All Stories

  1. Langerhans-Zell-Histiozytose
  2. Tumoren der Schilddrüse
  3. Leukocyte Adhesion Defect Type I: Delayed Umbilical Cord Separation, a Surplus of Cells, and a Deficit of Defense
  4. Disease response criteria in Langerhans cell histiocytosis: a global view
  5. The Diligent Lego Player with Talocalcaneal Callosities
  6. The ECHO recommendations for dealing with vinblastine shortage affecting standard treatment of systemic Langerhans cell histiocytosis
  7. Therapiestrategien bei Kindern und Jugendlichen mit Langerhanszell Histiozytosen
  8. Aktualisierte AWMF Leitlinie zur Diagnostik und Therapie der Langerhanszell Histiozytose (LCH) im Kindes- und Jugendalter
  9. Clinicogenomic associations in childhood Langerhans cell histiocytosis: an international cohort study
  10. Outcome of haematopoietic cell transplantation in children with lysosomal acid lipase deficiency: a study on behalf of the EBMT Inborn Errors Working Party
  11. Essential medicines for childhood cancer in Europe: a pan-European, systematic analysis by SIOPE
  12. Concurrence of a kinase‐dead BRAF and an oncogenic KRAS gain‐of‐function mutation in juvenile xanthogranuloma
  13. Whole‐body magnetic resonance imaging for staging Langerhans cell histiocytosis in children and young adults
  14. Fröschlein im Mund: eine Blickdiagnose?
  15. SARS-CoV-2 Associated Pediatric Inflammatory Multisystem Syndrome With a High Prevalence of Myocarditis – A Multicenter Evaluation of Clinical and Laboratory Characteristics, Treatment and Outcome
  16. Vemurafenib acts as a molecular on-off switch governing systemic inflammation in Langerhans cell histiocytosis
  17. Additive Prognostic Impact of Gastrointestinal Involvement in Severe Multisystem Langerhans Cell Histiocytosis
  18. Training von Basisreanimationsmaßnahmen (Newborn Life Support, Paediatric Basic Life Support)
  19. EVOLUTION OF TREATMENT OF CHILDREN WITH LANGERHANS CELL HISTIOCYTOSIS
  20. Langerhans Cell Histiocytosis of the Orbit: Spectrum of Clinical and Imaging Findings
  21. Novel Compound Heterozygous Mutations in Two Families With Bernard–Soulier Syndrome
  22. Stem cell transplantation for children with hemophagocytic lymphohistiocytosis: results from the HLH-2004 study
  23. Hemolytic anemia due to the unstable hemoglobin Wien: manifestations and long-term course in the largest pedigree identified to date
  24. The coming of age of Langerhans cell histiocytosis
  25. Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study
  26. Epigenomics and Single-Cell Sequencing Define a Developmental Hierarchy in Langerhans Cell Histiocytosis
  27. Low mortality and short‐term morbidity in very preterm infants in Austria 2011–2016
  28. Mycoplasma-pneumoniae -assoziierte Mukositis mit Hautbeteiligung - ein Fallbericht
  29. Successful Treatment with SCIG of a Child with Refractory Chronic ITP
  30. Mycoplasma pneumoniae -associated mucositis with cutaneous involvement - a case report
  31. Longitudinal assessment of peripheral blood BRAFV600E levels in patients with Langerhans cell histiocytosis
  32. Langerhans cell histiocytosis in children
  33. Langerhans cell histiocytosis in children
  34. An update on the treatment of pediatric-onset Langerhans cell histiocytosis through pharmacotherapy
  35. Histiozytäre Erkrankungen
  36. Confirmed efficacy of etoposide and dexamethasone in HLH treatment: long-term results of the cooperative HLH-2004 study
  37. Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis
  38. A consensus review on malignancy-associated hemophagocytic lymphohistiocytosis in adults
  39. Central Nervous System Langerhans Cell Histiocytosis
  40. Targeted inhibition of the MAPK pathway: emerging salvage option for progressive life-threatening multisystem LCH
  41. The Non-Langerhans Cell Histiocytoses (Rare Histiocytoses) – Clinical Aspects and Therapeutic Approaches
  42. Insights into the pathogenesis of Langerhans cell histiocytosis
  43. Current treatment of Langerhans cell histiocytosis
  44. Management of chronic immune thrombocytopenia in children and adolescents: lessons from an Austrian national cross-sectional study of 81 patients
  45. Two Novel Missense Mutations and a 5bp Deletion in the Erythroid-Specific Promoter of thePKLRGene in Two Unrelated Patients With Pyruvate Kinase Deficient Transfusion-Dependent Chronic Nonspherocytic Hemolytic Anemia
  46. Cladribine and cytarabine in refractory multisystem Langerhans cell histiocytosis: results of an international phase 2 study
  47. Malignancy-associated haemophagocytic lymphohistiocytosis in children and adolescents
  48. Treatment of Langerhans cell histiocytosis: it is time to learn from the past
  49. Lack of bone lesions at diagnosis is associated with inferior outcome in multisystem langerhans cell histiocytosis of childhood
  50. Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel
  51. Polycythaemia-inducing mutations in the erythropoietin receptor (EPOR): mechanism and function as elucidated by epidermal growth factor receptor-EPOR chimeras
  52. Histiozytosen
  53. Polycythemia-Inducing Mutations In The Erythropoietin Receptor (EPOR): Mechanism and Function Elucidated By EGFR– EPOR Chimeras
  54. Genetic Basis of Congenital Erythrocytosis
  55. Sequential decisions on FAS sequencing guided by biomarkers in patients with lymphoproliferation and autoimmune cytopenia
  56. Hypertrophic Obstructive Cardiomyopathy in an Infant With an Adrenocortical Tumor
  57. Radiological features of thymic langerhans cell histiocytosis
  58. Therapy prolongation improves outcome in multisystem Langerhans cell histiocytosis
  59. Treatment of Epstein Barr virus-induced haemophagocytic lymphohistiocytosis with rituximab-containing chemo-immunotherapeutic regimens
  60. Ferritin concentrations correlate to outcome of hematopoietic stem cell transplantation but do not serve as biomarker of graft-versus-host disease
  61. Stem cell transplantation after reduced-intensity conditioning for sickle cell disease
  62. Notch is active in Langerhans cell histiocytosis and confers pathognomonic features on dendritic cells
  63. Langerhans cell histiocytosis (LCH): Guidelines for diagnosis, clinical work-up, and treatment for patients till the age of 18 years
  64. Isolated cutaneous Langerhans cell histiocytosis in a premature baby: What is the optimal approach?
  65. Langerhans-Zell-Histiozytose
  66. Pulmonary Involvement in Pediatric-Onset Multisystem Langerhans Cell Histiocytosis: Effect on Course and Outcome
  67. Langerhans cell histiocytosis: pragmatic empirism on the road to rational cure
  68. Long‐term outcome of hypothalamic pituitary tumors in Langerhans cell histiocytosis
  69. Kopf- und Halstumore im Kindesalter
  70. Newly diagnosed immune thrombocytopenia in children and adults: a comparative prospective observational registry of the Intercontinental Cooperative Immune Thrombocytopenia Study Group
  71. Variant alleles of cytokine genes influence risk and clinical course of Langerhans cell histiocytosis
  72. Multisystem Langerhans Cell Histiocytosis in Children
  73. Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency
  74. Evaluating Bleeding Severity in Children with newly Diagnosed Immune Thrombocytopenia: A Pilot Study
  75. Novel TMPRSS6 mutations associated with iron-refractory iron deficiency anemia (IRIDA)
  76. Transcobalamin II deficiency at birth
  77. Subcutaneous anti-d globulin application is a safe treatment option of immune thrombocytopenia in children
  78. Diabetes insipidus in Langerhans cell histiocytosis: When is treatment indicated?
  79. Granulocyte Transfusions in Children and Young Adults
  80. A Syndrome with Congenital Neutropenia and Mutations inG6PC3
  81. Reactivations in Multisystem Langerhans Cell Histiocytosis: Data of the International LCH Registry
  82. Clinical and molecular characterisation of a prospectively collected cohort of children and adolescents with polycythemia vera
  83. Improved outcome in multisystem Langerhans cell histiocytosis is associated with therapy intensification
  84. Bone marrow assessment in Langerhans cell histiocytosis
  85. Extramedullary plasmacytoma of the adenoids
  86. Importance of allogeneic T-cells for disease control after stem cell transplantation for high-risk Langerhans cell histiocytosis
  87. Severe Anemia Owing to Occult Pulmonary Hemorrhage
  88. Central nervous system‐related permanent consequences in patients with Langerhans cell histiocytosis
  89. Critical issues concerning splenectomy for chronic idiopathic thrombocytopenic purpura in childhood
  90. Skelettbefall bei Langerhanszellhistiozytose
  91. Central diabetes insipidus: Is it Langerhans cell histiocytosis of the pituitary stalk? A diagnostic pitfall
  92. Improved outcome of treatment-resistant high-risk Langerhans cell histiocytosis after allogeneic stem cell transplantation with reduced-intensity conditioning
  93. Modern Imaging Methods for the Assessment of Langerhans' Cell Histiocytosis—Associated Neurodegenerative Syndrome: Case Report
  94. Risk factors for diabetes insipidus in langerhans cell histiocytosis
  95. Histiocytosis following T-acute lymphoblastic leukemia: A BFM study
  96. Langerhans cell histiocytosis in neonates
  97. Pineal gland abnormalities in Langerhans cell histiocytosis
  98. Central diabetes insipidus as presenting symptom of Langerhans cell histiocytosis
  99. Course and clinical impact of magnetic resonance imaging findings in diabetes insipidus associated with Langerhans cell histiocytosis
  100. Demonstration of CD1a positive cells in the cerebrospinal fluid—A clue to diagnosis of isolated Langerhans cell histiocytosis of the hypothalamic—pituitary axis?
  101. IVIG Treatment of Adenovirus Infection-Associated Macrophage Activation Syndrome in a Two-Year-Old Boy: Case Report and Review of the Literature
  102. Immunosuppressive treatment for chemotherapy-resistant multisystem langerhans cell histiocytosis
  103. IVIG Treatment of Adenovirus Infection-Associated Macrophage Activation Syndrome in a Two-Year-Old Boy: Case Report and Review of the Literature
  104. Response to initial treatment of multisystem langerhans cell histiocytosis: An important prognostic indicator
  105. Pattern and course of single-system disease in Langerhans cell histiocytosis data from the DAL-HX 83- and 90-study
  106. Statement of current majority practices in graft-versus-host disease prophylaxis and treatment in children
  107. Treatment of Multisystem Langerhans Cell Histiocytosis. Results of the DAL-HX 83 and DAL-HX 90 Studies
  108. Cyclosporine A therapy for multisystem Langerhans cell histiocytosis
  109. Cyclosporine A therapy for multisystem Langerhans cell histiocytosis
  110. Leucocyte transfusions from rhG-CSF or prednisolone stimulated donors for treatment of severe infections in immunocompromised neutropenic patients
  111. OCCURRENCE OF ACUTE NONLYMPHOBLASTIC LEUKEMIA IN TWO GIRLS AFTER TREATMENT OF RECURRENT, DISSEMINATED LANGERHANS CELL HISTIOCYTOSIS
  112. Transplantation activities and treatment strategies in paediatric stem cell transplantation centres: a report from the EBMT Working Party on Paediatric Diseases
  113. A single Centre Experience with allogeneic Stem Cell Transplantation for Severe Aplastic Anaemia in Childhood