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1. JAK inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID/EBMT-IEWP retrospective study

2. Impact of cytomegalovirus infection prior to hematopoietic stem cell transplantation in children with inborn errors of immunity

3. Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

4. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

5. Scalable GMP-compliant gene correction of CD4+ T cells with IDLV template functionally validated in vitro and in vivo

6. Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes

7. A Multi‑Center, Open‑Label, Single‑Arm Trial to Evaluate the Efficacy, Pharmacokinetics, and Safety and Tolerability of IGSC 20% in Subjects with Primary Immunodeficiency

12. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

13. JAK inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID/EBMT-IEWP retrospective study

15. Correction to: A Multi-center, Open-Label, Single-Arm Trial to Evaluate the Efficacy, Pharmacokinetics, and Safety and Tolerability of IGSC 20% in Subjects with Primary Immunodeficiency

16. 211 Biallelic null mutations in PPM1D cause a novel combined immunodeficiency with severe neurodevelopmental defects

17. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

18. Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutations

19. Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes

20. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

26. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

34. Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

35. Increased proportions of γδ T lymphocytes in atypical SCID associate with disease manifestations

37. High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers

41. Acquired and Innate Immunity Impairment and Severe Disseminated Mycobacterium genavense Infection in a Patient With a NF-κB1 Deficiency

42. Extreme Phenotypes With Identical Mutations: Two Patients With Same Non-sense NHEJ1 Homozygous Mutation

49. High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers

50. Prospective neonatal screening for severe T‐ and B‐lymphocyte deficiencies in Seville

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