52 results on '"Zieger B"'
Search Results
2. Next-generation sequencing identified different types of Hermansky-Pudlak syndrome associated with phenotype variability
3. Newly diagnosed children and adolescents with haemophilia A and B in Germany – the GEPHARD study of the `Standing Commission Paediatrics of the Society for Thrombosis and Haemostasis Research
4. Preliminary Results Regarding Effects of Pulsatility during Extracorporeal Circulation on In Vitro Hemolysis, Coagulation and Inflammation
5. Detection and Differential Diagnosis of Prekallikrein Deficiency: Genetic Study of New Families and Systematic Review of the Literature
6. Novel likely Pathogenic Variant in the Second Calcium Binding Domain of αIIb (Subunit of αIIbβ3) in a Patient with Glanzmann Thrombasthenia
7. Successful Treatment with Emicizumab of a Patient with Severe Haemophilia A and Factor VIII Inhibitors
8. Acquired von Willebrand Syndrome in Pediatric Patients during Mechanical Circulatory Support
9. Hypertrophe Pylorusstenose: Sonographisches Monitoringbei konservativer intravenöserTherapie mit Atropinsulfat
10. Successful Allogenic Haematopoietic Stem Cell Transplantation in a Boy with Hemophilia A and MDS-RAEB
11. Cardiac thrombus with risk of fulminant pulmonary embolism in paediatric antiphospholipid syndrome
12. Tubular Aggregate Myopathy Caused by an Autosomal Dominant Mutation in ORAI 1 Gene
13. Increased Levels of von Willebrand Factor Parameters in Children with Febrile Seizures
14. A Bladder Hematoma Mimicking a Tumor in a Newborn with Severe Hemophilia A
15. Acute “Tumour-like” Tongue Haematoma: The Challenge to Diagnose Haemophilia A
16. Platelet repellent properties of hydrogel coatings on polyurethane coated glass surfaces
17. Platelet function in patients with left ventricular assist devices
18. Diagnose angeborener Störungen der Thrombozytenfunktion
19. Genetics of inherited platelet disorders
20. Therapie hereditärer Thrombozytopathien
21. A Prospective Randomised Control Study: Reduction of Children's Pain Expectation Using a Picture Book during Blood Withdrawal
22. Coincidence of 2 Severe Chronic Diseases: Presymptomatic Diagnosis of Wilson Disease in A Boy With Severe Haemophilia A
23. Molecular Genetic Analysis of a Patient with Moderate Hemophilia A and Psychomotor Developmental Delay
24. Homozygous Point Mutations in Platelet Glycoprotein ITGA2B Gene as Cause of Glanzmann Thrombasthenia in 2 Families
25. Prophylactic Use of Clopidogrel in Paediatric Cardiac Patients
26. Acquired Von Willebrand Syndrome (AVWS) and bleeding complications in long-term patients with Ventricular Assist Devices (VAD)
27. Anterior Spinal Artery Syndrome in a 13-Year-Old Boy 8 Days After Taekwondo-Fight: Vascular Obliteration Due to Vessel Lesion or Thrombophilia?
28. Progressive Thrombosis in a 13-Year-Old Girl with Trisomy 21 Under Therapy with Low Molecular Weight Heparin
29. Acquired Von Willebrand Syndrome in patients with extra-corporeal life support (ECLS) or membrane oxygenation (ECMO)
30. Diagnostic and Therapeutic Considerations on Inherited Platelet Disorders in Neonates and Children
31. Compound Heterozygosity of the Protein S-Gene as a Cause of Severe Cerebral Sinovenous Thrombosis in a 7-Year-Old Child
32. Compound Heterozygous Mutations in 2 Siblings with Hermansky-Pudlak Syndrome Type 1 (HPS1)
33. Novel Homozygous Mutation (c.175delG) in Platelet GlycoproteinITGA2BGene as Cause of Glanzmann's Thrombasthenia Type I
34. Acquired von Willebrand syndrome and hemolysis in different types of ventricular assist devices (VAD) and total artificial heart (TAH)
35. Erfolgreiche konservative Therapie einer akzidentellen Perforation des Ösophagus bei einem extremen Frühgeborenen
36. Septins, a Novel Group of GTP-binding Proteins – Relevance in Hemostasis, Neuropathology and Oncogenesis
37. Lepirudin Treatment in a Girl with Iliac Vein Thrombosis, Severe Pulmonary Embolism and Suspected Heparin-induced Thrombocytopenia (HIT) II
38. Wirksamkeit einer kurzen psychologischen Vorbereitung von Kindern bei Blutentnahmen mithilfe eines Büchleins
39. Heparin induzierte Thrombozytopenie Typ II (HIT II) bei 6-jährigem Jungen nach Herzoperation verursacht Multiorganversagen
40. Lepirudin treatment in a boy with suspected HIT II after surgery because of tetralogy of Fallot
41. A large Swiss family with Bernard-Soulier syndrome
42. Hemolysis in patients with ventricular assist devices (VAD): Systems differ significantly
43. Identification of a novel factor X deletion in combination with a missense mutation in the F10 gene
44. Hämostaseologischer Notfall bei einem extremen Frühgeborenen: großer intrakardialer Thrombus mit konsekutivem Kreislaufversagen und Anurie – erfolgreiche Lysetherapie mit Urokinase und Orgaran
45. Fallbericht: Interstitielles Emphysem mit ausgeprägter Pseudozystenbildung bei einem Frühgeborenen trotz milder Beatmung
46. Referenzradiologie des Nephroblastoms: Diagnosegenauigkeit und Bedeutung für die präoperative Chemotherapie
47. Erhöhte systolische Blutdruckwerte aber nicht ein atherogenes Lipidprofil erhöhen die Intima media Dicke (IMD) bei gut eingestellten Kindern und Jugendlichen mit Typ 1 Diabetes mellitus
48. Perioperative Risiken und Therapie bei Epilepsiepatienten
49. Hypertrophe Pylorusstenose: Sonographisches Monitoringbei konservativer intravenöserTherapie mit Atropinsulfat
50. Ein einfacher Test für die Bestimmung der Funktion des Von-Willebrand-Faktors: die Kollagenbindungsaktivität
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