All Stories

  1. Updates on Pediatric Hepatoblastoma
  2. ADPKD, COVID-19, and Apixaban: The Treacherous Intracystic Bleeding – A Letter on Apixaban Causing Hepatic Cystic Bleeding by Shehi et al.
  3. Non-celiac wheat sensitivity: rationality and irrationality of a gluten-free diet in individuals affected with non-celiac disease: a review
  4. Lupus nephritis and Zimmerhackl’s legacy for histopathology: A milestone for clinical trials and reduction of interobserver disagreement
  5. The tumor microenvironment may trigger lymphoproliferation in cardiac myxoma
  6. Mathematical models in nursing research
  7. Cancer Stem Cells and their Management in Cancer Therapy
  8. Hypophosphatasia: The Unusual Presentation
  9. Targeting NLRP3 inflammasome in an animal model for Coronavirus Disease 2019 (COVID‐19) caused by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS‐CoV‐2)
  10. Face Masks Are Beneficial Regardless of the Level of Infection in the Fight Against COVID-19
  11. Low bone mineral density in HIV-positive young Italians and migrants
  12. Kefir microbial composition is a deciding factor in the physiological impact of kefir in a mouse model of obesity
  13. Association between factor V Leiden mutation and recurrent pregnancy loss in the middle east countries: a Newcastle–Ottawa meta-analysis
  14. MMP inhibitors attenuate doxorubicin cardiotoxicity by preventing intracellular and extracellular matrix remodeling
  15. Pediatrics: An Evolving Concept for the 21st Century
  16. Pediatric Sarcoidosis: A Review with Emphasis on Early Onset and High-Risk Sarcoidosis and Diagnostic Challenges
  17. Congenital Segmental Intestinal Dilatation: A 25-Year Review with Long-Term Follow-up at the Medical University of Innsbruck, Austria
  18. The microbiota of the bilio-pancreatic system: a cohort, STROBE-compliant study
  19. EPAS 1, congenital heart disease, and high altitude: disclosures by genetics, bioinformatics, and experimental embryology
  20. Endothelial cells of different organs exhibit heterogeneity in von Willebrand factor expression in response to hypoxia
  21. Tuberculosis evolution and climate change: How much work is ahead?
  22. Aluminum Exposure from Parenteral Nutrition: Early Bile Canaliculus Changes of the Hepatocyte
  23. Sialidosis: A Review of Morphology and Molecular Biology of a Rare Pediatric Disorder
  24. Fine Needle Aspiration Cytology for Neck Masses in Childhood. An Illustrative Approach
  25. Vanishing gastroschisis: Good outcome after a 10-year follow-up
  26. Bactibilia in diseases of the biliary tract and pancreatic gland in patients older than 80 years: a STROBE-retrospective cohort study in a teaching hospital in Italy
  27. Chloroquine-induced cardiomyopathy: a reversible cause of heart failure
  28. Antioxidants and Cancer: Theories, Techniques, and Trials in Preventing Cancer
  29. Co-ingestion of aspirin and acetaminophen promoting fulminant liver failure: A critical review of Reye syndrome in the current perspective at the dawn of the 21st century
  30. Co-ingestion of willow bark tea and acetaminophen associated with fatal infantile fulminant liver failure
  31. “English Disease”: Historical Notes on Rickets, the Bone–Lung Link and Child Neglect Issues
  32. Pediatric adrenal cortical carcinomas: Histopathological criteria and clinical trials. A systematic review
  33. Complete Maxillo-Mandibular Syngnathia in a Newborn with Multiple Congenital Malformations
  34. Eosinophilic Esophagitis
  35. Malignant pleural mesothelioma in a child
  36. Adenovirus necrotizing hepatitis complicating atypical teratoid rhabdoid tumor
  37. Laboratory Procedures Update on Hirschsprung Disease
  38. Differential Expression of Sonic Hedgehog Protein in Human Hepatocellular Carcinoma and Intrahepatic Cholangiocarcinoma
  39. R&D Implementation in a Department of Laboratory Medicine and Pathology: A Systematic Review Based on Pharmaceutical Companies
  40. Parenteral Soy Oil and Fish Oil Emulsions
  41. A Case of an Infant With Compound Heterozygous Mutations for Hypertrophic Cardiomyopathy Producing a Phenotype of Left Ventricular Noncompaction
  42. Factor V Leiden mutation in women with early recurrent pregnancy loss: a meta-analysis and systematic review of the causal association
  43. Mitochondriome and Cholangiocellular Carcinoma
  44. Anderson-Fabry cardiomyopathy: prevalence, pathophysiology, diagnosis and treatment
  45. Residues 240–250 in the C-Terminus of the Pirh2 Protein Complement the Function of the RING Domain in Self-Ubiquitination of the Pirh2 Protein
  46. A Balanced IL-1β Activity Is Required for Host Response to Citrobacter rodentium Infection
  47. Low-Dose Vasopressin Improves Cardiac Function in Newborn Piglets With Acute Hypoxia-Reoxygenation
  48. A case of lamin A/C mutation cardiomyopathy with overlap features of ARVC: A critical role of genetic testing
  49. Mimickers and tumours in the lower urinary tract: Need for a more efficient vigilance?
  50. Appendix carcinoids in childhood: Long-term experience at a single institution in Western Canada and systematic review
  51. Epithelial Cell Extrusion Leads to Breaches in the Intestinal Epithelium
  52. Recurrent anencephaly: A case report and examination of theVANGL1andFOXN1genes
  53. BMP-binding protein twisted gastrulation is required in mammary gland epithelium for normal ductal elongation and myoepithelial compartmentalization
  54. UBE4B: A Promising Regulatory Molecule in Neuronal Death and Survival
  55. Infantile myofibromatosis: report on a family with autosomal dominant inheritance and variable penetrance
  56. Branchiooculofacial Syndrome and Bilateral Ectopic Thymus: Report of a Family
  57. Holoprosencephaly-Polydactyly (Pseudotrisomy 13) Syndrome: Case Report and Diagnostic Criteria
  58. Angiogenic Remodeling in Pediatric EoE Is Associated With Increased Levels of VEGF-A, Angiogenin, IL-8, and Activation of the TNF-α–NFκB Pathway
  59. Sacrococcygeal Teratoma – a single center study of 43 years (1968–2011) including follow-up data and histopathological reevaluation of specimens
  60. FOXO3/FKHRL1 is activated by 5-aza-2-deoxycytidine and induces silenced caspase-8 in neuroblastoma
  61. Twisted gastrulation expression in cholangiocellular and hepatocellular carcinoma
  62. Clear Cell Variant of Embryonal Rhabdomyosarcoma: Report of an Unusual Retroperitoneal Tumor—Case Report and Literature Review
  63. Early versus delayed cyclosporine treatment in cardiac recovery and intestinal injury during resuscitation of asphyxiated newborn piglets
  64. OTX2mutations contribute to the otocephaly-dysgnathia complex
  65. Hepatic ultrastructure in a neonatal piglet model of intestinal failure-associated liver disease (IFALD)
  66. Canine Liver Transplantation Model and the Intermediate Filaments of the Cytoskeleton of the Hepatocytes
  67. Vasopressin improves systemic hemodynamics without compromising mesenteric perfusion in the resuscitation of asphyxiated newborn piglets: a dose–response study
  68. Mitochondrial DNA Depletion Syndrome-An Unusual Reason for Interstage Attrition after the Modified Stage 1 Norwood Operation
  69. Tolerability of inhaled N-chlorotaurine in an acute pig streptococcal lower airway inflammation model
  70. Medical management of motility disorders in patients with intestinal failure: a focus on necrotizing enterocolitis, gastroschisis, and intestinal atresia
  71. Familial adenomatous polyposis with concurrent metastatic appendiceal carcinoid and ovarian cystoadenoma
  72. Papillary renal cell carcinoma: report of a rare entity in childhood with review of the clinical management
  73. PRRX1 is mutated in a fetus with agnathia-otocephaly
  74. Decreased Apoptosis Despite Severe CD4 Depletion in the Thymus of a Human Immunodeficiency Virus-1 Infected Child
  75. Novel Neonatal Piglet Models of Surgical Short Bowel Syndrome With Intestinal Failure
  76. Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture
  77. The expression of twisted gastrulation in postnatal mouse brain and functional implications
  78. Solid-pseudopapillary tumor of the pancreas in a 12-year-old girl – 7 years follow-up and histopathological reevaluation: Case report and subject review
  79. Histology and synchrotron radiation-based microtomography of the inner ear in a molecularly confirmed case of CHARGE syndrome
  80. β-cell development and turnover during prenatal life in humans
  81. Epidermal Growth Factor Receptor Expression in Human Fetal Cochlea With Turner Syndrome
  82. The cochlea in fetuses with neural tube defects
  83. Tolerability of inhaled N-chlorotaurine in the pig model
  84. Immunohistochemical detection of polyductin and co-localization with liver progenitor cell markers during normal and abnormal development of the intrahepatic biliary system and in adult hepatobiliary carcinomas
  85. Successful treatment of severe juvenile microscopic polyangiitis with rituximab
  86. Discordant Outcomes in a Case of Parvovirus B19 Transmission Into Both Dichorionic Twins
  87. Does perinatal asphyxia induce apoptosis in the inner ear?
  88. Diagnosis of Hepatic Iron Overload
  89. Morphology Studies of the Human Fetal Cochlea in Turner Syndrome
  90. Pelizaeus Merzbacher disease: morphological analysis of the vestibulo-cochlear system
  91. Osteogenic sarcoma (osteosarcoma) in the elderly: Tumor delineation and predisposing conditions
  92. External quality assurance as a revalidation method for pathologists in pediatric histopathology: Comparison of four international programs
  93. Unravelling the parental origin and mechanism of formation of the 47,XY,i(X)(q10) Klinefelter karyotype variant
  94. Spatial and temporal dynamics of innervation during the development of fetal human pancreas
  95. Biliary-Type Cytokeratin Pattern in a Canine Isolated Perfused Liver Transplantation Model
  96. Bile duct to portal space ratio and ductal plate remnants in liver disease of infants aged less than 1 year
  97. Errata
  98. Congenital Fibrosarcoma as Cause for Fetal Anemia: Prenatal Diagnosis and in utero Treatment
  99. An Unusual Case of Intrauterine Symptomatic Neonatal Liver Failure
  100. Metastasizing Renal Cell Carcinoma Developing in a Congenital Ectopic and Dysplastic Kidney
  101. CD1a down-regulation in primary invasive ductal breast carcinoma may predict regional lymph node invasion and patient outcome
  102. Kidney transplantation in patients suffering from hereditary complete complement C4 deficiency
  103. Atrial natriuretic peptide and CD34 overexpression in human idiopathic dilated cardiomyopathies
  104. Fetal Distribution of 5α-Reductase 1 and 5α-Reductase 2, and Their Input on Human Prostate Development
  105. Pure esophageal atresia with normal outer appearance: case report
  106. Fatal circumstances of human herpesvirus 6 infection: transcriptosome data analysis suggests caution in implicating HHV-6 in the cause of death
  107. Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T>C, p.M226T; c.1112C>T, p.T371I) of the tissue-nonspecific alkaline phosphatase gene
  108. Chemotherapeutic treatment of a pregnant patient with ovarian dysgerminoma
  109. Conjoined Epigastric Heteropagus Twins: Excision of a Parasitic Twin from the Anterior Abdominal Wall of Her Sibling
  110. Growth curves of the fetal prostate based on three-dimensional reconstructions: a correlation with gestational age and maternal testosterone levels
  111. Reevaluation of the Fetal Muscle Development of the Vesical Trigone
  112. Systemischer Lupus erythematodes im Kindes- und Jugendalter
  113. First localization and biochemical identification of chromogranin B- and secretoneurin-like immunoreactivity in the fetal human vagal/nucleus solitary complex
  114. Successful transplantation in a child with rapid progression of autosomal recessive polycystic kidney disease associated with a novel mutation
  115. Pregnancy outcomes in women with or without placental malaria infection
  116. Juvenile sarcoidosis presenting as Crohn’s Disease
  117. Nuclear Insulin-Like Growth Factor Binding Protein-3 Induces Apoptosis and Is Targeted to Ubiquitin/Proteasome–Dependent Proteolysis
  118. ARLTS1 variants and melanoma risk
  119. Comparative expression analysis of Pax3 and Pax7 during mouse myogenesis
  120. Local application of a collagen type I/hyaluronate matrix and growth and differentiation factor 5 influences the closure of osteochondral defects in a minipig model by enchondral ossification
  121. Single Nucleotide Polymorphisms (SNPs): History, Biotechnological Outlook and Practical Applications
  122. Use of Recombinant Factor VIIa(Novoseven??) in Combination with Other Coagulation Products Led to a Thrombotic Occlusion of the Truncus Brachiocephalicus in a Neonate Supported by Extracorporal Membrane Oxygenation
  123. DMBT1 expression and glycosylation during the adenoma–carcinoma sequence in colorectal cancer
  124. DETECTION OF CHLAMYDIA PNEUMONIAE IN LIVER TRANSPLANT PATIENTS WITH CHRONIC ALLOGRAFT REJECTION
  125. Effects of Local Application of Growth and Differentiation Factor-5 (GDF-5) in a Full-thickness Cartilage Defect Model
  126. Das Wachstumsfaktorkomposit aus GDF-5 und mineralisiertem Kollagen verbessert die Ausheilung einer H�ftkopfnekrose
  127. Human brain of preterm infants after hypoxic-ischaemic injuries: no evidence of a substantial role for apoptosis by using a fine-tuned ultrasound-guided neuropathological analysis
  128. Pathology Quiz Case
  129. Iron overload in adult Hfe-deficient mice independent of changes in the steady-state expression of the duodenal iron transporters DMT1 and Ireg1/ferroportin
  130. Severe Anemia in a 25-Day-Old Infant Due to Gastric Teratoma with Focal Neuroblastoma
  131. Agnathia-otocephaly complex: Report of three cases with involvement of two different Carnegie stages
  132. Identification of a CTL4 /Neu1 fusion transcript in a sialidosis patient
  133. A new animal model of femoral head necrosis induced by intraosseous injection of ethanol
  134. Eosinophilic Enterocolitis in a Patient With Rheumatoid Arthritis
  135. Single nucleotide insertion in the 5′-untranslated region of hepatitis C virus with clearance of the viral RNA in a liver transplant recipient during acute hepatitis B virus superinfection
  136. Prenatal diagnosis and fetal pathology in a Turkish family harboring a novel nonsense mutation in the lysosomal α-N-acetyl-neuraminidase (sialidase) gene
  137. Ellis-van Creveld syndrome: a generalized dysplasia of enchondral ossification
  138. Perinatal hypophosphatasia: Radiology, pathology and molecular biology studies in a family harboring a splicing mutation (648+1A) and a novel missense mutation (N400S) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene
  139. Study of the Malformation of Ductal Plate of the Liver in Meckel Syndrome and Review of Other Syndromes Presenting with this Anomaly
  140. Akardius oder "Twin-Reversed-Arterial-Perfusion"-Sequenz
  141. The remodeling of the primitive human biliary system
  142. Central nervous system in twin reversed arterial perfusion sequence with special reference to examination of the brain in acardius anceps
  143. The central nervous system in microcephalic primordial dwarfism: Is there a characteristic developmental brain pathology in Seckel or Seckel-like syndrome?
  144. Norman-Roberts syndrome: prenatal diagnosis and autopsy findings
  145. Stage IIa Cervix Carcinoma with Metastasis to the Heart: Report of a Case with Immunohistochemistry, Flow Cytometry, and Virology Findings
  146. Huge Fetal Sacrococcygeal Teratoma with a Completely Formed Eye and Intratumoral DNA Ploidy Heterogeneity
  147. The distribution of HBV, HCV and HGV among livers with fulminant hepatic failure of different aetiology
  148. Short-rib-polydactyly syndrome type Verma-Naumoff-Le Marec in a fetus with histological hallmarks of type Saldino-Noonan but lacking internal organ abnormalities
  149. Ruhender Knorpel und Epiphysenfuge bei diastrophischer Dysplasie
  150. Utilization of magnetic resonance imaging in autopsy planning with specimen preservation for thoraco-omphalopagus symmetricus conjoined twins
  151. Case report: prenatal diagnosis of diastrophic dysplasia by ultrasound at 21 weeks of gestation in a mother with massive obesity
  152. Telencephalosynapsis (synencephaly) and rhombencephalosynapsis with posterior fossa ventriculocele (‘Dandy-Walker cyst’): an unusual aberrant syngenetic complex
  153. Wilms' tumor arising in a multicystic kidney
  154. Purification of alpha-1-antitrypsin monomer by preparative electrophoresis.