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1. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

2. Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival

3. TCF3 haploinsufficiency defined by immune, clinical, gene-dosage, and murine studies

4. Outcome of hematopoietic cell transplantation for DNA double-strand break repair disorders

5. Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival

6. Executive Summary of the Consensus Document on the Diagnosis and Management of Patients with Primary Immunodeficiencies

7. The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis

8. Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases

10. Patients with CD3G mutations reveal a role for human CD3γ in Treg diversity and suppressive function

11. Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group

12. Correction to: Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group

13. Autoimmune lymphoproliferative syndrome due to somatic FAS mutation (ALPS-sFAS) combined with a germline caspase-10 (CASP10) variation

14. Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes

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

17. Regulatory B cells in patients suffering from inborn errors of immunity with severe immune dysregulation

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

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

23. Clinical Non-penetrance Associated with Biallelic Mutations in the RNase H2 Complex.

24. Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies

25. Executive Summary of the Consensus Document on the Diagnosis and Management of Patients with Primary Immunodeficiencies

26. Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies

27. Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes

28. Meningococcal B Vaccine Immunogenicity in Children With Defects in Complement and Splenic Function

29. The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis

31. Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children

32. Wiskott-Aldrich syndrome: a retrospective study of 577 patients defines the genotype as a predictive biomarker for disease severity and survival

33. Wiskott-Aldrich Syndrome: A Retrospective Study on 575 Patients Analyzing the Impact of Splenectomy, Stem Cell Transplantation, or No Definitive Treatment on Frequency of Disease-Related Complications and Physician-Perceived Quality of Life

34. Patients with CD3Gmutations reveal a role for human CD3γ in Tregdiversity and suppressive function

35. A Case of IL-7R Deficiency Caused by a Novel synonymous Mutation and Implications for Mutation screening in sCID Diagnosis.

37. Autoantibodies against type I IFNs in patients with critical influenza pneumonia

39. Patients with CD3G mutations reveal a role for human CD3γ in Treg diversity and suppressive function.

40. Imaging of bronchial pathology in antibody deficiency

41. Non-apoptotic FAS signaling controls mTOR activation and extrafollicular maturation in human B cells.

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