Sergio Damian Rosenzweig


Ontology type: schema:Person     


Person Info

NAME

Sergio Damian

SURNAME

Rosenzweig

Publications in SciGraph latest 50 shown

  • 2021-11-17 CARD9 Expression Pattern, Gene Dosage, and Immunodeficiency Phenotype Revisited in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2021-10-16 A Double-Blind, Placebo-Controlled, Crossover Study of Magnesium Supplementation in Patients with XMEN Disease in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2021-06-21 A variant in human AIOLOS impairs adaptive immunity by interfering with IKAROS in NATURE IMMUNOLOGY
  • 2021-06-16 Correction to: Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel Mutations in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2021-05-25 Complicated Diagnosis and Treatment of HA20 due to Contiguous Gene Deletions involving 6q23.3 in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2021-05-05 Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel Mutations in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2021-04-14 Abnormal SCID Newborn Screening and Spontaneous Recovery Associated with a Novel Haploinsufficiency IKZF1 Mutation in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2021-01-03 IKAROS-Associated Diseases in 2020: Genotypes, Phenotypes, and Outcomes in Primary Immune Deficiency/Inborn Errors of Immunity in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-11-27 N-Glycan Modification in Covid-19 Pathophysiology: In vitro Structural Changes with Limited Functional Effects in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-11-02 POLD1 Deficiency Reveals a Role for POLD1 in DNA Repair and T and B Cell Development in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-10-01 Expanding the Clinical Phenotype of Chronic Granulomatous Disease: a Female Patient with a De Novo Mutation in CYBB in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-09-09 Correction to: A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-08-19 A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-07-17 Progressive B Cell Loss in Revertant X-SCID in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-01-20 Targeted therapy guided by single-cell transcriptomic analysis in drug-induced hypersensitivity syndrome/drug reaction with eosinophilia and systemic symptoms: A case report in NATURE MEDICINE
  • 2019-12-11 Mutations that prevent caspase cleavage of RIPK1 cause autoinflammatory disease in NATURE
  • 2018-08-20 Old vaccines, new diseases: when BCG meets SPPL2a in NATURE IMMUNOLOGY
  • 2018-05-21 Correction to: Use of Genetic Testing for Primary Immunodeficiency Patients in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2018-04-19 Use of Genetic Testing for Primary Immunodeficiency Patients in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2018-03-27 Ikaros family zinc finger 1 regulates dendritic cell development and function in humans in NATURE COMMUNICATIONS
  • 2017-12-06 Decreased Lymphocytes and Increased Risk for Infection are Common in Endogenous Pediatric Cushing Syndrome in PEDIATRIC RESEARCH
  • 2017-10-27 Erratum: Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic disease in NATURE GENETICS
  • 2017-06-19 Germline hypomorphic CARD11 mutations in severe atopic disease in NATURE GENETICS
  • 2017-06-16 Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes in SCIENTIFIC REPORTS
  • 2017-04-04 First Case of X-Linked Moesin Deficiency Identified After Newborn Screening for SCID in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2016-12-02 Phagocytes Defects in PRIMARY IMMUNODEFICIENCY DISEASES
  • 2016-09-26 Ataxia telangiectasia associated with nodular regenerative hyperplasia in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2016-07-07 Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation in GENETICS IN MEDICINE
  • 2016-07-02 A Novel Mutation in IKBKG/NEMO Leads to Ectodermal Dysplasia with Severe Immunodeficiency (EDA-ID) in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2016-02-11 Application of Flow Cytometry in the Evaluation of Primary Immunodeficiencies in THE INDIAN JOURNAL OF PEDIATRICS
  • 2015-03-27 Caspase-8 Deficiency Presenting as Late-Onset Multi-Organ Lymphocytic Infiltration with Granulomas in two Adult Siblings in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2014-10-29 Gain of Function Mutations of PIK3CD as a Cause of Primary Sclerosing Cholangitis in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2014-09-17 A de novo nonsense mutation in the tyrosine kinase lyn in a patient with an early onset autoinflammatory phenotype in PEDIATRIC RHEUMATOLOGY
  • 2014-09-17 TRNT1 missense mutations define an autoinflammatory disease characterized by recurrent fever, severe anemia, and b-cell immunodeficiency in PEDIATRIC RHEUMATOLOGY
  • 2014-03-08 Mutations in PIK3CD Can Cause Hyper IgM Syndrome (HIGM) Associated with Increased Cancer Susceptibility in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2014-01-09 News from the CIS Executive Committee in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2012-09-27 Defects in Innate Immunity: Receptors and Signaling Components in CLINICAL CASES IN PRIMARY IMMUNODEFICIENCY DISEASES
  • 2012-09-27 Disorders of Phagocytic Cells in CLINICAL CASES IN PRIMARY IMMUNODEFICIENCY DISEASES
  • 2012-09-27 Immune Dysregulation Diseases in CLINICAL CASES IN PRIMARY IMMUNODEFICIENCY DISEASES
  • 2011-08-04 Recent Insights into the Pathobiology of Innate Immune Deficiencies in CURRENT ALLERGY AND ASTHMA REPORTS
  • 2008-08-02 Clinical and Molecular Analysis of 49 Patients With X-linked Agammaglobulinemia From A Single Center in Argentina in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2008-01-12 Inflammatory Manifestations in Chronic Granulomatous Disease (CGD) in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2008 Phagocytes Defects in PRIMARY IMMUNODEFICIENCY DISEASES
  • 2007-01-19 Efficacy and Tolerability of an Argentine Intravenous Immunoglobulin in Pediatric Patients with Primary Immunodeficiency Diseases in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2005-05-29 Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations in NATURE GENETICS
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