Lista de obras - Nina K Serwas - Dominio Público Uruguay

Atypical manifestation of LRBA deficiency with predominant IBD-like phenotype

artículo científico publicado en 2015

CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis.

artículo científico publicado en 2017

CEBPE-Mutant Specific Granule Deficiency Correlates With Aberrant Granule Organization and Substantial Proteome Alterations in Neutrophils.

artículo científico publicado en 2018

Clinical and Molecular Heterogeneity of RTEL1 Deficiency

artículo científico publicado en 2017

Clinical features of interleukin 10 receptor gene mutations in children with very early-onset inflammatory bowel disease

artículo científico publicado en 2015

Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 Deficiency

artículo científico publicado en 2017

Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis

scientific article published on 15 July 2019

Human NF-κB1 Haploinsufficiency and Epstein-Barr Virus-Induced Disease-Molecular Mechanisms and Consequences.

artículo científico publicado en 2017

INFLAMMATORY BOWEL DISEASE-LIKE PHENOTYPE IN A YOUNG GIRL WITH PROLIDASE DEFICIENCY: A NEW SPECTRUM OF CLINICAL MANIFESTATION.

artículo científico publicado en 2015

ITK Deficiency: How can EBV be Treated Before Lymphoma?

artículo científico publicado en 2015

Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia

artículo científico publicado en 2014

Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections

artículo científico publicado en 2015

Long-term remission after allogeneic hematopoietic stem cell transplantation in LPS-responsive beige-like anchor (LRBA) deficiency

artículo científico publicado en 2014

Multiple Presentations of LRBA Deficiency: a Single-Center Experience.

artículo científico publicado en 2017

Novel Mutation in CECR1 Leads to Deficiency of ADA2 with Associated Neutropenia

artículo científico publicado en 2018

Publisher Correction: Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis

scientific article published on 02 October 2019

Lista de obras de Nina K Serwas

Atypical manifestation of LRBA deficiency with predominant IBD-like phenotype

CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis.

CEBPE-Mutant Specific Granule Deficiency Correlates With Aberrant Granule Organization and Substantial Proteome Alterations in Neutrophils.

Clinical and Molecular Heterogeneity of RTEL1 Deficiency

Clinical features of interleukin 10 receptor gene mutations in children with very early-onset inflammatory bowel disease

Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 Deficiency

Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis

Human NF-κB1 Haploinsufficiency and Epstein-Barr Virus-Induced Disease-Molecular Mechanisms and Consequences.

INFLAMMATORY BOWEL DISEASE-LIKE PHENOTYPE IN A YOUNG GIRL WITH PROLIDASE DEFICIENCY: A NEW SPECTRUM OF CLINICAL MANIFESTATION.

ITK Deficiency: How can EBV be Treated Before Lymphoma?

Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia

Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections

Long-term remission after allogeneic hematopoietic stem cell transplantation in LPS-responsive beige-like anchor (LRBA) deficiency

Multiple Presentations of LRBA Deficiency: a Single-Center Experience.

Novel Mutation in CECR1 Leads to Deficiency of ADA2 with Associated Neutropenia

Publisher Correction: Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis