All Stories

  1. Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency

    Article • Blood Coagulation & Fibrinolysis, June 2016, Wolters Kluwer Health

    Prof Nejat Akar

  2. A comparison of healthy infants and adults with respect to indirect microparticle activity and the parameters of thrombin generation test

    Article • Turkish Journal of Hematology, May 2016, Journal of Clinical Research of Pediatric Endocrinology

    Prof Nejat Akar

  3. SPATIALLY EXPLICIT MODELS TO INVESTIGATE GEOGRAPHIC PATTERNS IN THE DISTRIBUTION OF FORENSIC STRs

    Article • May 2016, Cold Spring Harbor Laboratory Press

    Prof Nejat Akar

  4. Grandmother's effect on child weight in Turkish Community

    Article • Journal of Paediatrics and Child Health, April 2016, Wiley

    Prof Nejat Akar

  5. Detection of TET2, KRAS and CBL variants by Next Generation Sequencing and analysis of their correlation with JAK2 and FLT3 in childhood AML

    Article • Egyptian Journal of Medical Human Genetics, April 2016, Elsevier

    Prof Nejat Akar

  6. Hemoglobin H Disease in Turkey: Experience from Eight Centers

    Article • Turkish Journal of Hematology, February 2016, Journal of Clinical Research of Pediatric Endocrinology

    Prof Nejat Akar

  7. Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling Study

    Article • PLoS ONE, February 2016, PLOS

    Prof Nejat Akar

  8. Endothelial Cells, Ankaferd Hemostat, And Estradiol

    Article • Turkish Journal of Hematology, January 2016, Journal of Clinical Research of Pediatric Endocrinology

    Prof Nejat Akar

  9. Antibacterial activities of Ankaferd Hemostat (ABS) on ‘Shiga toxin producing Escherichia coli’ and other pathogens significant in foodborne diseases

    Article • Turkish Journal of Hematology, January 2016, Journal of Clinical Research of Pediatric Endocrinology

    Prof Nejat Akar

  10. The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β0-thalassaemia homozygotes

    Article • British Journal of Haematology, January 2016, Wiley

    Prof Nejat Akar

  11. Qualitative/Chemical Analyses of Ankaferd Hemostat and Its Antioxidant Content in Synthetic Gastric Fluids

    Article • BioMed Research International, January 2016, Hindawi Publishing Corporation

    Prof Nejat Akar, Dr Umit Yavuz Malkan

  12. A Further Note on the Thalassemia Screening Program in the Muğla Region of Turkey

    Article • Hemoglobin, November 2015, Taylor & Francis

    Prof Nejat Akar

  13. Radioactive fallout and neural tube defects

    Article • Egyptian Journal of Medical Human Genetics, October 2015, Elsevier

    Prof Nejat Akar

  14. C-type lectin domain family 12, member A: A common denominator in Behçet’s syndrome and acute gouty arthritis

    Article • Medical Hypotheses, August 2015, Elsevier

    Prof Nejat Akar

  15. Prothrombotic risk factors in childhood migraine and comparison of acetylsalicyclic acid and propranolol in prophylactic therapy

    Article • Journal of Pediatric Neurology, July 2015, Thieme Publishing Group

    Prof Nejat Akar

  16. Behçet’s disease as cause of sinovenous thrombosis in a pediatric patient

    Article • Journal of Pediatric Neurology, July 2015, Thieme Publishing Group

    Prof Nejat Akar

  17. Phylogeographic Refinement and Large Scale Genotyping of Human Y Chromosome Haplogroup E Provide New Insights into the Dispersal of Early Pastoralists in the African Continent

    Article • Genome Biology and Evolution, June 2015, Oxford University Press (OUP)

    Prof Nejat Akar

  18. A Novel Beta Globin Gene Polymorphism in Turkish Population: IVS-II 706 G>A

    Article • The Journal of Pediatric Research, June 2015, Journal of Clinical Research of Pediatric Endocrinology

    Prof Nejat Akar

  19. A Novelist Observation on Emotional Deprivation During the First World War

    Article • The Journal of Pediatric Research, March 2015, Journal of Clinical Research of Pediatric Endocrinology

    Prof Nejat Akar

  20. Nail Destruction Due to “Print Correction Fluid”

    Article • The Journal of Pediatric Research, March 2015, Journal of Clinical Research of Pediatric Endocrinology

    Prof Nejat Akar

  21. Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann’s thrombasthenia

    Article • Platelets, March 2015, Taylor & Francis

    Prof Nejat Akar

  22. High iron content of Ankaferd hemostat as a clue for its hemostatic action of red blood cell origin

    Article • Blood Coagulation & Fibrinolysis, March 2015, Wolters Kluwer Health

    Prof Nejat Akar

  23. Ankaferd Blood Stopper induces apoptosis and regulates PAR1 and EPCR expression in human leukemia cells

    Article • Egyptian Journal of Medical Human Genetics, January 2015, Elsevier

    Prof Nejat Akar

  24. γA gene repeats polymorphism for the analysis of haplotypes of abnormal hemoglobins

    Article • Thalassemia Reports, September 2014, PAGEPress Publications

    Prof Nejat Akar

  25. Hemoglobin Lansing (Alpha) [HBA2 CD87 (HIS>GLU) (C>A)] in a Turkish Individual Resulting from Another Nucleotide Substitution

    Article • Turkish Journal of Hematology, September 2014, Journal of Clinical Research of Pediatric Endocrinology

    Prof Nejat Akar

  26. Does FVL have an effect on longevity?

    Article • Egyptian Journal of Medical Human Genetics, July 2014, Elsevier

    Prof Nejat Akar

  27. An Updated Review of Abnormal Hemoglobins in the Turkish Population

    Article • Turkish Journal of Hematology, March 2014, Journal of Clinical Research of Pediatric Endocrinology

    Prof Nejat Akar

  28. Evaluation of indirect microparticle activity and parameters of thrombin generation test in healthy infants

    Article • Thrombosis Research, February 2014, Elsevier

    Prof Nejat Akar

  29. Naming a novel hemoglobin variant

    Article • Journal of Chromatography B, February 2014, Elsevier

    Prof Nejat Akar

  30. An Analysis of the Levels of the Soluble Form of the Endothelial Protein C Receptor in Children with Henoch–Schönlein Purpura

    Article • Pediatric Hematology and Oncology, December 2013, Taylor & Francis

    Prof Nejat Akar

  31. Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls

    Article • European Journal of Epidemiology, July 2013, Springer Science + Business Media

    Prof Nejat Akar

  32. Genome-Wide Transcriptional Reorganization Associated with Senescence-to-Immortality Switch during Human Hepatocellular Carcinogenesis

    Article • PLoS ONE, May 2013, PLOS

    Dr Rengul Cetin-Atalay, Dr Gokhan YILDIZ, Prof Nejat Akar

  33. A novel protein C inhibitor gene mutation in pediatric stroke patients after bone marrow transplantation

    Article • Molecular Biology Reports, May 2013, Springer Science + Business Media

    Prof Nejat Akar

  34. Blood group genotyping in multi-transfused patients

    Article • Transfusion and Apheresis Science, April 2013, Elsevier

    Prof Nejat Akar

  35. Endothelial Protein C Receptor and Pediatric Arterial Stroke

    Article • Turkish Journal of Hematology, March 2013, Journal of Clinical Research of Pediatric Endocrinology

    Prof Nejat Akar

  36. Three thousand eight hundred-year-old toys of the Hittites

    Article • European Journal of Pediatrics, January 2013, Springer Science + Business Media

    Prof Nejat Akar

  37. Effect of Factor V Leiden on Thrombosis in Childhood Leukemia

    Article • Open Journal of Blood Diseases, January 2013, Scientific Research Publishing, Inc,

    Prof Nejat Akar

  38. Identification of four common α-thalassemia gene deletions among a group with hemoglobinopathies in Sétif population, Algeria

    Article • Pteridines, January 2013, De Gruyter

    Prof Nejat Akar

  39. C0369 Factor V leiden and prothrombin 20210A mutations among turkish pediatric leukemia patients

    Article • Thrombosis Research, October 2012, Elsevier

    Prof Nejat Akar

  40. C0377 Does FVL have an effect on longevity?

    Article • Thrombosis Research, October 2012, Elsevier

    Prof Nejat Akar

  41. Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis

    Article • PROTEOMICS - CLINICAL APPLICATIONS, August 2012, Wiley

    Prof Nejat Akar

  42. Inherited Thrombophilia in Pediatric Ischemic Stroke: An Egyptian Study

    Article • Pediatric Neurology, August 2012, Elsevier

    Prof Nejat Akar

  43. Methylenetetrahydrofolate reductase gene polymorphism in type 1 diabetes mellitus: Relationship to microvascular complications

    Article • Egyptian Journal of Medical Human Genetics, June 2012, Elsevier

    Prof Nejat Akar

  44. Intron F G79A Polymorphism of the Protein Z Gene in Turkish Behçet Patients

    Article • Current Eye Research, May 2012, Taylor & Francis

    Prof Nejat Akar

  45. Neural Tube Defects in Algeria

    Article • March 2012, IntechOpen

    Prof Nejat Akar

  46. To the editor

    Article • World Journal of Pediatrics, January 2012, Springer Science + Business Media

    Prof Nejat Akar

  47. Endothelial Dysfunction and Vitamin D Levels in Kidney Allograft Recipients

    Article • Turkish Nephrology Dialysis Transplantation, January 2012, Turkish Nephrology Dialysis Transplantation

    Prof Nejat Akar

  48. Nutritional Factors, Homocysteine and C677T Polymorphism of the Methylenetetrahydrofolate Reductase Gene in Algerian Subjects with Cardiovascular Disease

    Article • Pteridines, January 2012, De Gruyter

    Prof Nejat Akar

  49. TNF-α-308 G/A Polymorphism in Egyptian Budd-Chiari Syndrome Patients

    Article • Turkish Journal of Hematology, January 2012, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  50. First Observation of Hemoglobin M Saskatoon (�63 (E7) His>Tyr(C-T)) in the Iraqi Population

    Article • Turkish Journal of Hematology, January 2012, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  51. Dual Diverse Dynamic Reversible Actions of Ankaferd on EPCR and PAI-1 Inside Vascular Endothelial Cells With and Without LPS

    Article • Turkish Journal of Hematology, January 2012, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  52. A novel homozygous nucleotide deletion at JAK�2 gene in a pediatric B-cell precursor acute lymphoblastic leukemia

    Article • Turkish Journal of Hematology, January 2012, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  53. Factor V Leiden and Prothrombin 20210A Mutations among Turkish Pediatric Leukemia Patients

    Article • Leukemia Research and Treatment, January 2012, Hindawi Publishing Corporation

    Prof Nejat Akar

  54. The value of procalcitonin measurements in children with familial Mediterranean fever

    Article • Rheumatology International, November 2011, Springer Science + Business Media

    Prof Nejat Akar

  55. Role of ZIP14 (SLC39A14) gene histidine rich regions in neural tube defects

    Article • Egyptian Journal of Medical Human Genetics, November 2011, Elsevier

    Prof Nejat Akar

  56. Lipoprotein A Levels in Pediatric Migraine

    Article • Pediatric Neurology, October 2011, Elsevier

    Prof Nejat Akar

  57. Thrombotic gene polymorphisms and postoperative outcome after coronary artery bypass graft surgery

    Article • Journal of Cardiothoracic Surgery, September 2011, Springer Science + Business Media

    Prof Nejat Akar

  58. The Association of Protease Activated Receptor 1 gene −506 I/D Polymorphism with Disease-Free Survival in Breast Cancer Patients

    Article • Annals of Surgical Oncology, August 2011, Springer Science + Business Media

    Prof Nejat Akar

  59. The incidence of alpha-thalassemia in Iraqi Turks

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  60. The importance of studying inherited hematological disorders in ancient Anatolian populations

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  61. A novel 110 bp insertion in a patient with homocystinuria

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  62. First observation of MTHFR 678 C-A (Ala222Ala) single nucleotide polymorphism

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  63. The frequency of Factor V 1691G-A mutation in Iraqi Turks

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  64. Endothelial Protein C Receptor gene expression in a woman with homozygous EPCR 23 bp insertion

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  65. The frequency of FV G1691A and PT G20210A mutations in an Albanian population

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  66. The effects of Ankaferd Blood Stopper on transcription factors in HUVEC and erythrocyte protein profile

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  67. The effects of endothelial protein C receptor gene polymorphisms on sEPCR levels in venous thrombotic patients

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  68. Dual diverse dynamic reversible actions of Ankaferd on EPCR and PAI-1 inside vascular endothelial cells with and without LPS

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  69. First observation of hemoglobin Crete (B129 (H7) Ala>Pro) in Turkish population

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  70. The role of tumor necrosis factor-alpha -308 G/A and transforming growth factor-beta 1 -915 G/C polymorphisms in childhood idiopathic thrombocytopenic purpura

    Article • Turkish Journal of Hematology, August 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  71. Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis

    Article • Molecular Biology Reports, June 2011, Springer Science + Business Media

    Prof Nejat Akar

  72. Kikuchi-Fujimoto Disease Associated with Aseptic Meningitis: A Case Report

    Article • Çocuk Enfeksiyon Dergisi/Journal of Pediatric Infection, June 2011, AVES Publishing Co.

    Prof Nejat Akar

  73. Childhood migraine and hypercoagulopathy

    Article • British Journal of Haematology, May 2011, Wiley

    Prof Nejat Akar

  74. Hemoglobin alpha 2 gene +861 G>A polymorphism in Turkish population

    Article • Egyptian Journal of Medical Human Genetics, May 2011, Elsevier

    Prof Nejat Akar

  75. A novel MEFV gene mutation (A511V) in a Chilean FMF patient

    Article • Egyptian Journal of Medical Human Genetics, May 2011, Elsevier

    Prof Nejat Akar

  76. Protease activated receptor 1 gene −506 I / D polymorphism in cancer patients with and without venous thrombosis

    Article • European Journal Of Haematology, April 2011, Wiley

    Prof Nejat Akar

  77. Factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms and the risk of tamoxifen-associated thromboembolism in breast cancer patients

    Article • Thrombosis Research, April 2011, Elsevier

    Prof Nejat Akar

  78. The relation between soluble endothelial protein C receptor and factor VIII levels and FVIII/sEPCR index in healthy infants

    Article • Turkish Journal of Hematology, March 2011, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  79. Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents

    Article • Journal of Pediatric Endocrinology and Metabolism, January 2011, De Gruyter

    Prof Nejat Akar

  80. Thrombosis and risk factors

    Article • Turkish Journal of Hematology, December 2010, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  81. The incidence of alpha-thalassemia in Setif, Algeria

    Article • Turkish Journal of Hematology, December 2010, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  82. Association of Methylenetetrahydrofolate Reductase C677T and Cystathionine β-Synthase Polymorphisms in Cardiovascular Disease in the Algerian Population

    Article • Genetic Testing and Molecular Biomarkers, December 2010, Mary Ann Liebert Inc

    Prof Nejat Akar

  83. Functional proteomic analysis of Ankaferd® Blood Stopper

    Article • Turkish Journal of Hematology, June 2010, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  84. Ribosomal protein S19 - 631 insertion is an African-originated mutation

    Article • Turkish Journal of Hematology, June 2010, LookUs Bilisim, Ltd.

    Prof Nejat Akar

  85. Methylenetetrahydrofolate reductase C677T polymorphism in breast cancer risk

    Article • Breast Cancer Research and Treatment, May 2010, Springer Science + Business Media

    Prof Nejat Akar

  86. A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss

    Article • The American Journal of Human Genetics, May 2010, Elsevier

    Prof Nejat Akar

  87. A novel mutation of 5α-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment

    Article • European Journal of Pediatrics, February 2010, Springer Science + Business Media

    Prof Nejat Akar

  88. Association between the −402GA, −401GT, and −323ins10-bp polymorphisms of factor VII gene and breast cancer

    Article • Breast Cancer, January 2010, Springer Science + Business Media

    Prof Nejat Akar

  89. Hyperhomocysteinemia and C677T Polymorphism of Methylenetetrahydrofolate Reductase Gene in Patients with Cardiovascular Disease

    Article • Pteridines, January 2010, De Gruyter

    Prof Nejat Akar

  90. Association of the tumor necrosis factor-alpha −308 G/A polymorphism with nasal polyposis

    Article • European Archives of Oto-Rhino-Laryngology, December 2009, Springer Science + Business Media

    Prof Nejat Akar

  91. Soluble endothelial cell protein C receptor and thrombomodulin levels after renal transplantation

    Article • International Urology and Nephrology, October 2009, Springer Science + Business Media

    Prof Nejat Akar

  92. SOLUBLE ENDOTHELIAL PROTEIN C RECEPTOR LEVEL IN CHILDREN WITH SEPSIS

    Article • Pediatric Hematology and Oncology, September 2009, Taylor & Francis

    Prof Nejat Akar

  93. Relationship between functional promoter polymorphism in the XBP1 gene (−116C/G) and atherosclerosis, ischemic stroke and hyperhomocysteinemia

    Article • Molecular Biology Reports, August 2009, Springer Science + Business Media

    Prof Nejat Akar

  94. Response

    Article • Pediatric Neurology, July 2009, Elsevier

    Prof Nejat Akar

  95. Cerebral infarct associated with prothrombin gene G 20210 A variant in a Turkish child with cystic fibrosis: an unusual coexistence

    Article • European Journal Of Haematology, April 2009, Wiley

    Prof Nejat Akar

  96. Soluble endothelial protein C receptor levels in healthy population

    Article • Journal of Thrombosis and Thrombolysis, March 2009, Springer Science + Business Media

    Prof Nejat Akar

  97. A note on Homocysteine levels in Children

    Article • Thrombosis Research, March 2009, Elsevier

    Prof Nejat Akar

  98. Thrombophilic Risk Factors in Epileptic Children Treated with Valproic Acid

    Article • Pediatric Neurology, February 2009, Elsevier

    Prof Nejat Akar

  99. The effects of tamoxifen on homocysteine levels in breast cancer patients

    Article • Open Medicine, January 2009, De Gruyter

    Prof Nejat Akar

  100. SOLUBLE ENDOTHELIAL PROTEIN C RECEPTOR LEVEL IN CHILDREN WITH SEPSIS

    Article • Pediatric Hematology and Oncology, January 2009, Taylor & Francis

    Prof Nejat Akar

  101. Polymorphisms of 5,10-Methylenetetrahydrofolate Reductase and Cystathionine β-Synthase Genes as a Risk Factor for Neural Tube Defects in Sétif, Algeria

    Article • Pediatric Neurosurgery, January 2009, Karger Publishers

    Prof Nejat Akar

  102. Factor V Leiden and prothrombin G20210A polymorphisms are not associated with disease-free survival in breast cancer

    Article • Breast Cancer Research and Treatment, September 2008, Springer Science + Business Media

    Prof Nejat Akar

  103. The 19-bp deletion of dihydrofolate reductase (DHFR), methylenetetrahydrofolate reductase (MTHFR) C677T, Factor V Leiden, prothrombin G20210A polymorphisms in cancer patients with and without thrombosis

    Article • Annals of Hematology, August 2008, Springer Science + Business Media

    Prof Nejat Akar

  104. Soluble endothelial protein C receptor levels in Behçet patients with and without ocular involvement

    Article • Graefe s Archive for Clinical and Experimental Ophthalmology, July 2008, Springer Science + Business Media

    Prof Nejat Akar

  105. Dihydrofolate reductase (DHRF) 19-bp intron-1 deletion and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms in breast cancer

    Article • Breast Cancer Research and Treatment, May 2008, Springer Science + Business Media

    Prof Nejat Akar

  106. Serum Endothelial Monocyte-Activating Polypeptide–II: A Novel Biomarker in Patients with Non–Small-Cell Lung Cancer

    Article • Clinical Lung Cancer, May 2008, Elsevier

    Prof Nejat Akar

  107. Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome

    Article • Pediatrics International, April 2008, Wiley

    Prof Nejat Akar

  108. Thrombophilia-associated gene mutations in women with pregnancies complicated by fetal neural tube defects

    Article • International Journal of Gynecology & Obstetrics, February 2008, Wiley

    Prof Nejat Akar

  109. Intron F G79a polymorphism of the protein Z gene in cancer patients with and without thrombosis

    Article • Journal of Thrombosis and Thrombolysis, February 2008, Springer Science + Business Media

    Prof Nejat Akar

  110. Relationship between susceptibility to antimicrobials and virulence factors in paediatric Escherichia coli isolates

    Article • International Journal of Antimicrobial Agents, February 2008, Elsevier

    Prof Nejat Akar

  111. MEF2A Sequence Variants in Turkish Population

    Article • Clinical and Applied Thrombosis/Hemostasis, December 2007, SAGE Publications

    Prof Nejat Akar

  112. Prevalence of the MEFV Gene Mutations in Childhood Polyarteritis Nodosa

    Article • The Journal of Pediatrics, December 2007, Elsevier

    Prof Nejat Akar, Professor Ozgur KASAPCOPUR

  113. Off-pump coronary artery bypass graft surgery after stent implantation in a patient with combined thrombophilic risk factors

    Article • Canadian Journal of Cardiology, November 2007, Elsevier

    Prof Nejat Akar

  114. Vascular endothelial growth factor gene 936 C/T polymorphism in breast cancer patients

    Article • Cancer Immunology Immunotherapy, August 2007, Springer Science + Business Media

    Prof Nejat Akar

  115. Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

    Article • The American Journal of Human Genetics, February 2007, Elsevier

    Prof Nejat Akar

  116. EPCR gene A3 haplotype and elevated soluble endothelial protein C receptor (sEPCR) levels in Turkish pediatric stroke patients

    Article • Thrombosis Research, January 2007, Elsevier

    Prof Nejat Akar

  117. Idiopathic portal vein thrombosis and FVIII levels

    Article • Thrombosis Research, January 2007, Elsevier

    Prof Nejat Akar

  118. Vascular endothelial growth factor C936T polymorphism in cancer patients with thrombosis

    Article • American Journal of Hematology, January 2007, Wiley

    Prof Nejat Akar

  119. Serum Pro-Hepcidin Levels and Relationship with Ferritin in Healthy Non-Anaemic Infants

    Article • Acta Haematologica, January 2007, Karger Publishers

    Prof Nejat Akar

  120. HOMOZYGOUS 23-bp INSERTION OF ENDOTHELIAL PROTEIN C RECEPTOR GENE IN A CHILD WITH FATAL SEPSIS

    Article • Pediatric Hematology and Oncology, January 2007, Taylor & Francis

    Prof Nejat Akar

  121. A further note on thrombosis in patients with homozygous beta thalassemia

    Article • Thrombosis and Haemostasis, December 2006, Schattauer GmbH

    Prof Nejat Akar

  122. No Relation between Angiotensin-Converting Enzyme Gene Polymorphism and Pseudoexfoliation

    Article • Ophthalmic Research, November 2006, Karger Publishers

    Prof Nejat Akar

  123. Prevalence of Factor V 1691 G–A (Leiden) and prothrombin G20210A polymorphisms and the risk of venous thrombosis among cancer patients

    Article • Journal of Thrombosis and Thrombolysis, November 2006, Springer Science + Business Media

    Prof Nejat Akar

  124. Keratin 8 sequence variants in patients with pancreatitis and pancreatic cancer

    Article • Journal of Molecular Medicine, October 2006, Springer Science + Business Media

    Prof Nejat Akar

  125. Plasminogen activator inhibitor-1 gene 4G/5G polymorphism in cancer patients with and without thrombosis

    Article • Journal of Thrombosis and Thrombolysis, October 2006, Springer Science + Business Media

    Prof Nejat Akar

  126. Does SLC30A4 (ZNT4) gene exon 5 915 T-C alteration play a role in neural tube defects?

    Article • Trace Elements and Electrolytes, October 2006, Dustri-Verlgag Dr. Karl Feistle

    Prof Nejat Akar

  127. Noma

    Article • The Lancet, September 2006, Elsevier

    Prof Nejat Akar

  128. Pediatric Stroke, Homocysteine and MTHFR 677C-T and 1298 A-C

    Article • Journal of Pediatric Hematology/Oncology, September 2006, Wolters Kluwer Health

    Prof Nejat Akar

  129. Prothrombin Gene 20209 C>T Along with the First Description of a Homozygous Polymorphism at the 3′ Downstream Region +4 C>T in the Turkish Population

    Article • Laboratory Hematology, September 2006, Carden Jennings Publishing Co.

    Prof Nejat Akar

  130. Methylenetetrahydrofolate reductase 677 C-T and homocysteine levels in Turkish patients with pseudoexfoliation – response

    Article • Clinical and Experimental Ophthalmology, July 2006, Wiley

    Prof Nejat Akar

  131. A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis

    Article • Nature Genetics, May 2006, Nature

    Prof Nejat Akar

  132. 23-bp endothelial protein C receptor (EPCR) gene insertion mutation in cancer patients with and without thrombosis

    Article • American Journal of Hematology, January 2006, Wiley

    Prof Nejat Akar

  133. High plasma levels of factor VIII: An important risk factor for isolated pulmonary embolism

    Article • Respirology, January 2006, Wiley

    Prof Nejat Akar

  134. A germlinePTEN mutation with manifestations of prenatal onset and verrucous epidermal nevus

    Article • American Journal of Medical Genetics Part A, January 2006, Wiley

    Prof Nejat Akar

  135. Methylenetetrahydrofolate reductase 677 C-T and homocysteine levels in Turkish patients with pseudoexfoliation

    Article • Clinical and Experimental Ophthalmology, October 2005, Wiley

    Prof Nejat Akar

  136. Restriction Endonuclease Analysis as a Solution for Determining Rifampin Resistance Mutations by Automated DNA Sequencing in Heteroresistant Mycobacterium tuberculosis Strains

    Article • Microbial Drug Resistance, June 2005, Mary Ann Liebert Inc

    Prof Nejat Akar

  137. Is Tissue-Plasminogen Activator Gene Polymorphism a Risk Factor for Venous Thromboembolism in Every Population?

    Article • Journal of Thrombosis and Thrombolysis, February 2005, Springer Science + Business Media

    Prof Nejat Akar

  138. TNF-α −308G/A and IL-6 −174 G/C polymorphisms in the Turkish pediatric stroke patients

    Article • Thrombosis Research, January 2005, Elsevier

    Prof Nejat Akar

  139. Elevated FVIII and FIX level in a Behçet's disease patient with intracardiac thrombosis and pulmonary arterial aneurysms

    Article • Thrombosis Research, January 2005, Elsevier

    Prof Nejat Akar

  140. 657del5 Mutation of the Nijmegen Breakage Syndrome Gene (NBS1) in the Turkish Population

    Article • Human Biology, January 2005, Project Muse

    Prof Nejat Akar

  141. SERUM SOLUBLE TRANSFERRIN RECEPTOR IS A VALUABLE DIAGNOSTIC TOOL IN IRON DEFICIENCY OF BREATH-HOLDING SPELLS

    Article • Pediatric Hematology and Oncology, January 2005, Taylor & Francis

    Prof Nejat Akar

  142. FAMILIAL HIGH FACTOR VIII LEVEL IN A CHILD WITH NECROTIZING FASCIITIS COMPLICATING PRIMARY VARICELLA INFECTION

    Article • Pediatric Hematology and Oncology, January 2005, Taylor & Francis

    Prof Nejat Akar

  143. Sequence Analysis of rpoB Mutations in Rifampin-Resistant Clinical Mycobacterium tuberculosis Isolates from Turkey

    Article • Microbial Drug Resistance, December 2004, Mary Ann Liebert Inc

    Prof Nejat Akar

  144. The KBG syndrome: Confirmation of autosomal dominant inheritance and further delineation of the phenotype

    Article • American Journal of Medical Genetics Part A, September 2004, Wiley

    Prof Nejat Akar

  145. High factor VIII levels during attacks of familial Mediterranean fever

    Article • Pediatric Nephrology, July 2004, Springer Science + Business Media

    Prof Nejat Akar

  146. Natural immunity to Haemophilus influenzae type B in children of Ankara, Turkey

    Article • Pediatrics International, June 2004, Wiley

    Prof Nejat Akar

  147. Phylogeographic Analysis of Haplogroup E3b (E-M215) Y Chromosomes Reveals Multiple Migratory Events Within and Out Of Africa

    Article • The American Journal of Human Genetics, May 2004, Elsevier

    Prof Nejat Akar, Professor Martin Brian Richards

  148. Effect of Factor VIIIc Levels in Pediatric Stroke Patients

    Article • Pediatric Hematology and Oncology, January 2004, Taylor & Francis

    Prof Nejat Akar

  149. THE EFFECTS OF ACUTE INFECTION ON HEMATOLOGICAL PARAMETERS

    Article • Pediatric Hematology and Oncology, January 2004, Taylor & Francis

    Prof Nejat Akar

  150. Evaluation of Erythropoiesis by Serum Transferrin Receptor and Ferritin in Infants Aged 0–6 Months

    Article • Pediatric Hematology and Oncology, January 2004, Taylor & Francis

    Prof Nejat Akar

  151. Factor V Leiden and Prothrombin Gene 20210A Variant in Neonatal Thromboembolism and in Healthy Neonates and Adults: A Study in a Single Center

    Article • Pediatric Hematology and Oncology, December 2003, Taylor & Francis

    Prof Nejat Akar

  152. First observation of homozygous hemoglobin hamadan (B 56 (D7) GLY-ARG) and beta thalassemia (-29 G>A)- hemoglobin Hamadan combination in a Turkish family

    Article • American Journal of Hematology, November 2003, Wiley

    Prof Nejat Akar

  153. Effect of Twice Weekly Versus Daily Iron Treatment in Turkish Children with Iron Deficiency Anemia

    Article • Pediatric Hematology and Oncology, June 2003, Taylor & Francis

    Prof Nejat Akar

  154. Spectrum of GJB2 mutations in Turkey comprises both Caucasian and Oriental variants: Roles of parental consanguinity and assortative mating

    Article • Human Mutation, May 2003, Wiley

    Prof Nejat Akar

  155. Ligneous conjunctivitis, hydrocephalus, hydrocele, and pulmonary involvement in a child with homozygous type I plasminogen deficiency

    Article • European Journal of Pediatrics, April 2003, Springer Science + Business Media

    Prof Nejat Akar

  156. Factor VIII levels in children with thrombosis

    Article • Pediatrics International, April 2003, Wiley

    Prof Nejat Akar

  157. PT G20210A, factors V G1691A and 1299 His–Arg mutations and tamoxifen-associated thromboembolism in patients with breast cancer

    Article • Thrombosis Research, January 2003, Elsevier

    Prof Nejat Akar

  158. Letter to the Editor

    Article • Biological Trace Element Research, January 2003, Springer Science + Business Media

    Prof Nejat Akar

  159. Effect of Twice Weekly Versus Daily Iron Treatment in Turkish Children with Iron Deficiency Anemia

    Article • Pediatric Hematology and Oncology, January 2003, Taylor & Francis

    Prof Nejat Akar

  160. Serum amyloid A1 and tumor necrosis factor-alpha alleles in Turkish Familial Mediterranean Fever patients with and without amyloidosis

    Article • Amyloid, January 2003, Taylor & Francis

    Prof Nejat Akar

  161. Factor V Leiden and Prothrombin Gene 20210A Variant in Neonatal Thromboembolism and in Healthy Neonates and Adults: A Study in a Single Center

    Article • Pediatric Hematology and Oncology, January 2003, Taylor & Francis

    Prof Nejat Akar

  162. Factor V Gene (1691A and 4070G) and Prothrombin Gene 20210A Mutations in Patients with Behçet’s Disease

    Article • Pathophysiology of Haemostasis and Thrombosis, January 2003, Karger Publishers

    Prof Nejat Akar

  163. Factor V Leiden and prothrombin 20210 G-A mutations in controls and in patients with thromboembolic events during pregnancy or the puerperium

    Article • Archives of Gynecology and Obstetrics, November 2002, Springer Science + Business Media

    Prof Nejat Akar

  164. Three risk factors—high lipoprotein (a), elevated FVIII, and FV Leiden—in a pediatric Behçet's disease patient with deep vein thrombosis

    Article • Thrombosis Research, May 2002, Elsevier

    Prof Nejat Akar

  165. Does early erythropoietin therapy decrease transfusions in anemia of prematurity ?

    Article • The Indian Journal of Pediatrics, May 2002, Springer Science + Business Media

    Prof Nejat Akar

  166. Arthritis in children with familial Mediterranean fever

    Article • Rheumatology International, February 2002, Springer Science + Business Media

    Prof Nejat Akar

  167. RED BLOOD CELL INDEXES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS AND β-THALASSEMIA COMBINATION

    Article • Pediatric Hematology and Oncology, January 2002, Taylor & Francis

    Prof Nejat Akar

  168. HIGH LEVELS OF FVIII AND FIX IN A PEDIATRIC PATIENT WITH RETINAL ARTERY OCCLUSION

    Article • Pediatric Hematology and Oncology, January 2002, Taylor & Francis

    Prof Nejat Akar

  169. RECURRENT ARTERIAL THROMBOSIS IN A CHILD: Primary Antiphospholipid Antibody Syndrome

    Article • Pediatric Hematology and Oncology, January 2002, Taylor & Francis

    Prof Nejat Akar

  170. Tüberküloza Genetik Yatkınlık

    Article • Ankara Üniversitesi Tıp Fakültesi Mecmuası, January 2002, Ankara University

    Prof Nejat Akar

  171. Is high levels of factor VIII a possible risk factor for intracardiac thrombosis?

    Article • International Journal of Cardiology, December 2001, Elsevier

    Prof Nejat Akar

  172. E148Q of the MEFV Gene Causes Amyloidosis in Familial Mediterranean Fever Patients

    Article • PEDIATRICS, July 2001, American Academy of Pediatrics (AAP)

    Prof Nejat Akar

  173. Connexin 26 ( GJB2 ) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians

    Article • Human Genetics, May 2001, Springer Science + Business Media

    Prof Nejat Akar

  174. Common Mutations at the Homocysteine Metabolism Pathway and Pediatric Stroke

    Article • Thrombosis Research, April 2001, Elsevier

    Prof Nejat Akar

  175. The α2 Gene Alleles of the Platelet Collagen Receptor Integrin α2β1 in Turkish Children with Cerebral Infarct

    Article • Thrombosis Research, April 2001, Elsevier

    Prof Nejat Akar

  176. Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction

    Article • Clinical Cardiology, April 2001, Wiley

    Prof Nejat Akar

  177. Isolated recurrent pericarditis in a patient with familial Mediterranean fever

    Article • European Journal of Pediatrics, March 2001, Springer Science + Business Media

    Prof Nejat Akar

  178. Possible effects of antioxidant status on increased platelet aggregation in childhood iron-deficiency anemia

    Article • Pediatrics International, February 2001, Wiley

    Prof Nejat Akar

  179. Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome

    Article • European Journal of Pediatrics, February 2001, Springer Science + Business Media

    Prof Nejat Akar

  180. Plasminogen Activator Inhibitor-1 4G/5G Polymorphism in Turkish Children With Cerebral Infarct and Effect on Factor V 1691 A Mutation

    Article • Journal of Child Neurology, January 2001, Decker, Inc.

    Prof Nejat Akar

  181. Factor V 1691G-A mutation and high factor VIII levels in a patient with intracardiac thrombosis

    Article • European Journal of Pediatrics, November 2000, Springer Science + Business Media

    Prof Nejat Akar

  182. The Role of Prothrombotic Mutations in Patients with Buerger's Disease

    Article • Thrombosis Research, November 2000, Elsevier

    Prof Nejat Akar

  183. No association between Glu/Asp polymorphism of NOS3 gene and ischemic stroke

    Article • Neurology, August 2000, Wolters Kluwer Health

    Prof Nejat Akar

  184. MEFV mutations in multiplex families with familial Mediterranean fever: is a particular genotype necessary for amyloidosis?

    Article • Clinical Genetics, June 2000, Wiley

    Prof Nejat Akar

  185. Prothrombin Gene 20210 G→A and Factor V Arg 506 to Gln Mutation in a Patient with Buerger's Disease

    Article • Angiology, May 2000, SAGE Publications

    Prof Nejat Akar

  186. Spina bifida and common mutations at the homocysteine metabolism pathway

    Article • Clinical Genetics, March 2000, Wiley

    Prof Nejat Akar

  187. Effect Of Metylenetetrahydrofolate Reductase 677 C-T, 1298 A-C, and 1317 T-C on Factor V 1691 Mutation in Turkish Deep Vein Thrombosis Patients

    Article • Thrombosis Research, February 2000, Elsevier

    Prof Nejat Akar

  188. Factor V (his 1299 arg) in Turkish patients with venous thromboembolism

    Article • American Journal of Hematology, February 2000, Wiley

    Prof Nejat Akar

  189. Coexistence of factor V 1691 G-A and factor V 4070 A-G mutation in Turkish thromboembolic patients

    Article • American Journal of Hematology, January 2000, Wiley

    Prof Nejat Akar

  190. Factor V (His 1299 Arg) in Young Turkish Patients with Cerebral Infarct

    Article • Pathophysiology of Haemostasis and Thrombosis, January 2000, Karger Publishers

    Prof Nejat Akar

  191. Renal Amyloidosis in a Patient with Homozygous Sickle Cell Anemia and M694V/M694V Mutation

    Article • January 2000, Karger Publishers

    Prof Nejat Akar

  192. Effect of desferrioxamine on urinary copper and zinc excretion in β-thalassemia major patients

    Article • The Journal of Trace Elements in Experimental Medicine, January 2000, Wiley

    Prof Nejat Akar

  193. MEFV mutations in Turkish patients suffering from familial Mediterranean fever

    Article • Human Mutation, January 2000, Wiley

    Prof Nejat Akar

  194. Effect of desferrioxamine on urinary copper and zinc excretion in ?-thalassemia major patients

    Article • The Journal of Trace Elements in Experimental Medicine, January 2000, Wiley

    Prof Nejat Akar

  195. Recombinant human growth hormone treatment in children with thalassemia major

    Article • Pediatrics International, December 1999, Wiley

    Prof Nejat Akar

  196. Recombinant human growth hormone treatment in children with thalassemia major

    Article • Pediatrics International, December 1999, Wiley

    Prof Nejat Akar

  197. Feasibility of restriction enzyme protocols for the molecular diagnosis of abnormal hemoglobins in Turkish population

    Article • American Journal of Hematology, November 1999, Wiley

    Prof Nejat Akar

  198. Feasibility of restriction enzyme protocols for the molecular diagnosis of abnormal hemoglobins in Turkish population

    Article • American Journal of Hematology, November 1999, Wiley

    Prof Nejat Akar

  199. Plasma endothelin-1 levels in patients with left-to-right shunt with or without pulmonary hypertension

    Article • International Journal of Cardiology, July 1999, Elsevier

    Prof Nejat Akar

  200. Endothelial Nitric Oxide Synthase Intron 4, 27 bp Repeat Polymorphism in Turkish Patients with Deep Vein Thrombosis and Cerebrovascular Accidents

    Article • Thrombosis Research, April 1999, Elsevier

    Prof Nejat Akar

  201. Methylenetetrahydrofolate-Dehydrogenase 1958 G-A (R653 Q) Polymorphism in Turkish Patients with Venous Thromboembolism

    Article • Acta Haematologica, January 1999, Karger Publishers

    Prof Nejat Akar

  202. COEXISTENCE OF TWO PROTHROMBOTIC MUTATIONS, FACTOR V 1691 G-A AND PROTHROMBIN GENE 20210 G-A, AND THE RISK OF CEREBRAL INFARCT IN PEDIATRIC PATIENTS

    Article • Pediatric Hematology and Oncology, January 1999, Taylor & Francis

    Prof Nejat Akar

  203. Oxygen Free Radical-Dependent Increased Platelet Function in β-Thalassemia Major Patients

    Article • Thrombosis Research, December 1998, Elsevier

    Prof Nejat Akar

  204. Search for Genetic Factors Favoring Thrombosis in Turkish Population

    Article • Thrombosis Research, October 1998, Elsevier

    Prof Nejat Akar

  205. Prothrombin gene 20210 G-A mutation in the Turkish population

    Article • American Journal of Hematology, July 1998, Wiley

    Prof Nejat Akar

  206. Familial Mediterranean Fever — Amyloidosis and the Val726Ala Mutation

    Article • New England Journal of Medicine, April 1998, New England Journal of Medicine (NEJM/MMS)

    Prof Nejat Akar

  207. Further note for the discrimination of Hb C

    Article • American Journal of Hematology, February 1998, Wiley

    Prof Nejat Akar

  208. α-Thalassemia and Hereditary Spherocytosis in the Same Patient: The Interaction of two Diseases

    Article • Pediatric Hematology and Oncology, January 1998, Taylor & Francis

    Prof Nejat Akar

  209. Serum Interleukin-2 and Interleukin-6 Levels in IRON Deficiency Anemia

    Article • Pediatric Hematology and Oncology, January 1998, Taylor & Francis

    Prof Nejat Akar

  210. Effect of 1,2‐Dimethyl‐3‐Hydroxypyridin‐4‐One (L1) on zinc absorption

    Article • The Journal of Trace Elements in Experimental Medicine, January 1998, Wiley

    Prof Nejat Akar

  211. Effect of 1,2-Dimethyl-3-Hydroxypyridin-4-One (L1) on zinc absorption

    Article • The Journal of Trace Elements in Experimental Medicine, January 1998, Wiley

    Prof Nejat Akar

  212. Letter to the Editor: Serum Superoxide Dismutase Levels of Beta Thalassemia Patients and Effects of High Dosage of Intravenous Desferrioxamine Treatment on Superoxide Dismutase Levels

    Article • Pediatric Hematology and Oncology, January 1998, Taylor & Francis

    Prof Nejat Akar

  213. Further delineation of the molecular pathology of Wilson disease in the Mediterranean population

    Article • Human Mutation, January 1998, Wiley

    Prof Nejat Akar

  214. Further delineation of the molecular pathology of Wilson disease in the Mediterranean population

    Article • Human Mutation, January 1998, Wiley

    Prof Nejat Akar

  215. Differential Structuring of Human Populations for Homologous X and Y Microsatellite Loci

    Article • The American Journal of Human Genetics, September 1997, Elsevier

    Prof Nejat Akar

  216. Coffee beans pica causing iron and zinc deficiency

    Article • The Journal of Trace Elements in Experimental Medicine, January 1997, Wiley

    Prof Nejat Akar

  217. Pregnancy outcome of mothers with defective oral zinc tolerance test

    Article • The Journal of Trace Elements in Experimental Medicine, January 1997, Wiley

    Prof Nejat Akar

  218. Wilson disease mutations associated with uncommon haplotypes in mediterranean patients

    Article • Human Genetics, November 1996, Springer Science + Business Media

    Prof Nejat Akar

  219. Direct detection of Hb C (B6 Glu-Lys) byBseRI analysis

    Article • American Journal of Hematology, August 1996, Wiley

    Prof Nejat Akar

  220. Erythrocyte P Antigen in Beta Thalassemia Major Patients with Human Parvovirus-B19 Infection

    Article • Pediatric Hematology and Oncology, January 1996, Taylor & Francis

    Prof Nejat Akar

  221. A Case of Severe Thrombocytopenia Due to Parvovirus B19 Virus

    Article • Pediatric Hematology and Oncology, January 1996, Taylor & Francis

    Prof Nejat Akar

  222. Verification of Hb O-Arab [β121(GH4)GLU → LYS] by Dual Restriction Enzyme Analysis

    Article • Hemoglobin, January 1996, Taylor & Francis

    Prof Nejat Akar

  223. Tuberculous osteomyelitis: an unusual case of tuberculous infection in a child undergoing continuous ambulatory peritoneal dialysis

    Article • Pediatric Nephrology, August 1995, Springer Science + Business Media

    Prof Nejat Akar

  224. Effects of Calcitonin Therapy on Osteoporosis in Patients with Thalassemia

    Article • Acta Haematologica, January 1995, Karger Publishers

    Prof Nejat Akar

  225. p53 Codon 213 (A-G) Polymorphism in a Turkish Population

    Article • Pediatric Hematology and Oncology, January 1995, Taylor & Francis

    Prof Nejat Akar

  226. Incidence of Parvovirus B19 Infection Among Thalassemia Major Patients from Ankara, Turkey

    Article • Pediatric Hematology and Oncology, January 1995, Taylor & Francis

    Prof Nejat Akar

  227. GM-CSF in the treatment of Fanconi's anaemia

    Article • British Journal of Haematology, August 1994, Wiley

    Prof Nejat Akar

  228. Rapid Diagnosis Of Two β-Thalassemia Mutatlons: Frameshift Codon 5 (-CT) And Codon 6 (-A)

    Article • Pediatric Hematology and Oncology, January 1994, Taylor & Francis

    Prof Nejat Akar

  229. Burkitt's lymphoma between African and American types in Turkish children: Clinical, viral (EBV), and molecular studies

    Article • Medical and Pediatric Oncology, January 1993, Wiley

    Professor Ian T Magrath, Prof Nejat Akar

  230. Desferoxamine and Urinary Zinc Excretion in β-Thalassemia Major

    Article • Pediatric Hematology and Oncology, January 1993, Taylor & Francis

    Prof Nejat Akar

  231. Hemoglobinopathies in the District of Antalya, Turkey

    Article • Pediatric Hematology and Oncology, January 1993, Taylor & Francis

    Prof Nejat Akar

  232. Effects of zinc supplementation on somatomedin-C level, in beta thalassemia

    Article • American Journal of Hematology, October 1992, Wiley

    Prof Nejat Akar

  233. Doppler Color Flow Imaging for the Evaluation of Postsplenectomy Portal Vein Thrombosis in Pediatric Hematological Diseases

    Article • Pediatric Hematology and Oncology, January 1992, Taylor & Francis

    Prof Nejat Akar

  234. Ultrastructural Changes in the Mucosa of the Small Intestine in Patients with Geophagia (Prasadʼs Syndrome)

    Article • Journal of Pediatric Gastroenterology and Nutrition, August 1990, Wolters Kluwer Health

    Prof Nejat Akar

  235. NAEVUS OF JAMAICA

    Article • The Lancet, December 1988, Elsevier

    Prof Nejat Akar

  236. High incidence of neural tube defects in Bursa, Turkey

    Article • Paediatric and Perinatal Epidemiology, January 1988, Wiley

    Prof Nejat Akar

  237. ANOREXIA AND ZINC

    Article • The Lancet, October 1984, Elsevier

    Prof Nejat Akar

  238. Prevalence of Thalassemia and G6PD Deficiency in North Cyprus

    Article • Acta Haematologica, January 1984, Karger Publishers

    Prof Nejat Akar

  239. Modernizer of Turkey's Pediatrics: Albert Eckstein in Exile

    Article • SSRN Electronic Journal, Social Science Electronic Publishing

    Prof Nejat Akar

  240. Further Notes on Albert Eckstein: The Modernizer of Turkey's Pediatrics

    Article • SSRN Electronic Journal, Social Science Electronic Publishing

    Prof Nejat Akar