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1. Hypomorphic RAG deficiency: impact of disease burden on survival and thymic recovery argues for early diagnosis and HSCT

2. Wiskott-Aldrich Syndrome: A study on 577 patients defining the genotype as a predictive biomarker for disease severity

3. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

5. Acute chest syndrome in children with sickle cell disease: Data from a national AIEOP cohort identify priority areas of intervention in a hub‐and‐spoke system.

6. Acute chest syndrome in children with sickle cell disease: Data from a national AIEOP cohort identify priority areas of intervention in a hub‐and‐spoke system

7. ImmunoTyper-SR: A Novel Computational Approach for Genotyping Immunoglobulin Heavy Chain Variable Genes Using Short Read Data

9. ImmunoTyper-SR: A Novel Computational Approach for Genotyping Immunoglobulin Heavy Chain Variable Genes Using Short Read Data

10. Cutaneous barrier leakage and gut inflammation drive skin disease in Omenn syndrome

11. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

12. Multicenter analysis of neutrophil extracellular trap dysregulation in adult and pediatric COVID-19

13. Clonal Hematopoiesis Is Not Significantly Associated with Covid-19 Disease Severity

14. ImmunoTyper-SR: A computational approach for genotyping immunoglobulin heavy chain variable genes using short-read data

15. Immunopathological signatures in multisystem inflammatory syndrome in children and pediatric COVID-19

18. New data from the italian national register of congenital coagulopathies, 2016 annual survey

19. Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

20. Emergency management in patients with haemophilia A and inhibitors on prophylaxis with emicizumab: AICE practical guidance in collaboration with SIBioC, SIMEU, SIMEUP, SIPMeL and SISET

21. Physical activity improved by adherence to prophylaxis in an Italian population of children, adolescents and adults with severe haemophilia A: The SHAPE Study

26. X-linked recessive TLR7 deficiency in similar to 1% of men under 60 years old with life-threatening COVID-19

27. Autoantibodies neutralizing type I IFNs are present in similar to 4\% of uninfected individuals over 70 years old and account for similar to 20\% of COVID-19 deaths

28. Addressing the impact of SARS-CoV-2 infection in persons with congenital bleeding disorders: The Italian MECCOVID-19 study

29. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

30. Neutralizing type-I interferon autoantibodies are associated with delayed viral clearance and intensive care unit admission in patients with COVID-19

31. Risk factors for endocrine complications in transfusion-dependent thalassemia patients on chelation therapy with deferasirox: a risk assessment study from a multicentre nation-wide cohort

32. HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype-phenotype correlation

33. Consensus statements on vaccination in patients with haemophilia—Results from the Italian haemophilia and vaccinations (HEVA) project

35. Correspondence: Osteonecrosis in childhood acute lymphoblastic leukemia: a retrospective cohort study of the Italian Association of Pediatric Haemato-Oncology (AIEOP)

36. Second-line therapy in paediatric warm autoimmune haemolytic anaemia. Guidelines from the Associazione Italiana Onco-Ematologia Pediatrica (AIEOP)

37. EVENTI ACUTI NEI PAZIENTI CON MALATTIA DREPANOCITICADURANTE LA FASE I DEL LOCKDOWN: RISULTATI DELLA SURVEY NAZIONALE NEI CENTRI AIEOP

39. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

40. Use of Eltrombopag in Children With Chronic Immune Thrombocytopenia (ITP): A Real Life Retrospective Multicenter Experience of the Italian Association of Pediatric Hematology and Oncology (AIEOP)

43. B cell-helper neutrophils stimulate immunoglobulin diversification and production: 1.18

49. Neutrophils drive type-I interferon production and autoantibodies in Wiskott-Aldrich syndrome

50. Second-line therapy in paediatric warm autoimmune haemolytic anaemia. Guidelines from the Associazione Italiana Onco-Ematologia Pediatrica (AIEOP)

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