Lista de obras - Eirik Bratland - Dominio Público Uruguay

A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1.

artículo científico publicado en 2016

A novel cell-based assay for measuring neutralizing autoantibodies against type I interferons in patients with autoimmune polyendocrine syndrome type 1.

artículo científico publicado en 2014

Altered DNA methylation profile in Norwegian patients with Autoimmune Addison's Disease

artículo científico publicado en 2014

Altered Immune Activation and IL-23 Signaling in Response to Candida albicans in Autoimmune Polyendocrine Syndrome Type 1

artículo científico publicado en 2017

Analysis of cellular and humoral immune responses against cytomegalovirus in patients with autoimmune Addison's disease

artículo científico publicado en 2016

Anticommensal Responses Are Associated with Regulatory T Cell Defect in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients.

artículo científico publicado en 2016

Autoantibodies against aromatic amino acid hydroxylases in patients with autoimmune polyendocrine syndrome type 1 target multiple antigenic determinants and reveal regulatory regions crucial for enzymatic activity

artículo científico publicado en 2012

Autoimmune Addison's disease - An update on pathogenesis

artículo científico publicado en 2018

CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles

artículo científico publicado en 2014

Cellular immunity and immunopathology in autoimmune Addison's disease

scientific article published on 15 December 2010

Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease

artículo científico publicado en 2019

Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases

scientific journal article

Epitope mapping of human aromatic l-amino acid decarboxylase

artículo científico publicado en 2007

Functional studies of novel CYP21A2 mutations detected in Norwegian patients with congenital adrenal hyperplasia.

artículo científico publicado en 2014

High frequency of cytolytic 21-hydroxylase-specific CD8+ T cells in autoimmune Addison's disease patients

artículo científico publicado en 2014

Hypomagnesemia and functional hypoparathyroidism due to novel mutations in the Mg-channel TRPM6

artículo científico publicado en 2015

Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease

artículo científico publicado en 2019

Increased infiltration and tolerised antigen-specific CD8+ TEM cells in tumor but not peripheral blood have no impact on survival of HCMV+ glioblastoma patients.

artículo científico publicado en 2017

Induction of CXCL10 chemokine in adrenocortical cells by stimulation through toll-like receptor 3.

artículo científico publicado en 2012

Interleukin-2 and subunit alpha of its soluble receptor in autoimmune Addison's disease--an association study and expression analysis

artículo científico publicado en 2014

Peripheral Blood Cells from Patients with Autoimmune Addison's Disease Poorly Respond to Interferons In Vitro, Despite Elevated Serum Levels of Interferon-Inducible Chemokines.

artículo científico publicado en 2015

Potential Transcriptional Biomarkers to Guide Glucocorticoid Replacement in Autoimmune Addison's Disease

artículo científico publicado en 2021

Radioimmunoassay for autoantibodies against interferon omega; its use in the diagnosis of autoimmune polyendocrine syndrome type I

artículo científico publicado en 2008

Sequential bortezomib and temozolomide treatment promotes immunological responses in glioblastoma patients with positive clinical outcomes: A phase 1B study

artículo científico publicado en 2020

T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency

artículo científico publicado en 2009

The effect of types I and III interferons on adrenocortical cells and its possible implications for autoimmune Addison's disease

artículo científico publicado en 2014

The potential role for infections in the pathogenesis of autoimmune Addison's disease

artículo científico publicado en 2018

The purification and application of biologically active recombinant steroid cytochrome P450 21-hydroxylase: the major autoantigen in autoimmune Addison's disease

artículo científico publicado en 2009

The substrate-binding domain of 21-hydroxylase, the main autoantigen in autoimmune Addison's disease, is an immunodominant T cell epitope

artículo científico publicado en 2006

Lista de obras de Eirik Bratland

A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1.

A novel cell-based assay for measuring neutralizing autoantibodies against type I interferons in patients with autoimmune polyendocrine syndrome type 1.

Altered DNA methylation profile in Norwegian patients with Autoimmune Addison's Disease

Altered Immune Activation and IL-23 Signaling in Response to Candida albicans in Autoimmune Polyendocrine Syndrome Type 1

Analysis of cellular and humoral immune responses against cytomegalovirus in patients with autoimmune Addison's disease

Anticommensal Responses Are Associated with Regulatory T Cell Defect in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients.

Autoantibodies against aromatic amino acid hydroxylases in patients with autoimmune polyendocrine syndrome type 1 target multiple antigenic determinants and reveal regulatory regions crucial for enzymatic activity

Autoimmune Addison's disease - An update on pathogenesis

CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles

Cellular immunity and immunopathology in autoimmune Addison's disease

Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease

Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases

Epitope mapping of human aromatic l-amino acid decarboxylase

Functional studies of novel CYP21A2 mutations detected in Norwegian patients with congenital adrenal hyperplasia.

High frequency of cytolytic 21-hydroxylase-specific CD8+ T cells in autoimmune Addison's disease patients

Hypomagnesemia and functional hypoparathyroidism due to novel mutations in the Mg-channel TRPM6

Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease

Increased infiltration and tolerised antigen-specific CD8+ TEM cells in tumor but not peripheral blood have no impact on survival of HCMV+ glioblastoma patients.

Induction of CXCL10 chemokine in adrenocortical cells by stimulation through toll-like receptor 3.

Interleukin-2 and subunit alpha of its soluble receptor in autoimmune Addison's disease--an association study and expression analysis

Peripheral Blood Cells from Patients with Autoimmune Addison's Disease Poorly Respond to Interferons In Vitro, Despite Elevated Serum Levels of Interferon-Inducible Chemokines.

Potential Transcriptional Biomarkers to Guide Glucocorticoid Replacement in Autoimmune Addison's Disease

Radioimmunoassay for autoantibodies against interferon omega; its use in the diagnosis of autoimmune polyendocrine syndrome type I

Sequential bortezomib and temozolomide treatment promotes immunological responses in glioblastoma patients with positive clinical outcomes: A phase 1B study

T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency

The effect of types I and III interferons on adrenocortical cells and its possible implications for autoimmune Addison's disease

The potential role for infections in the pathogenesis of autoimmune Addison's disease

The purification and application of biologically active recombinant steroid cytochrome P450 21-hydroxylase: the major autoantigen in autoimmune Addison's disease

The substrate-binding domain of 21-hydroxylase, the main autoantigen in autoimmune Addison's disease, is an immunodominant T cell epitope