Lista de obras - Francisco Espinosa-Rosales

138 Transmission Pattern and Carriers Identification in Male Patients with Chronic Granulomatous Disease.

artículo científico publicado en 2012

604 Phenotypic and Functional Analysis of B Cells in Patients with Common Variable Immunodeficiency.

artículo científico publicado en 2012

A novel CD40LG deletion causes the hyper-IgM syndrome with normal CD40L expression in a 6-month-old child

artículo científico publicado en 2015

Advances in primary immunodeficiency diseases in Latin America: epidemiology, research, and perspectives

artículo científico

Advancing the management of primary immunodeficiency diseases in Latin America: Latin American Society for Immunodeficiencies (LASID) Initiatives.

artículo científico

Association analysis of the PTPN22 gene in childhood-onset systemic lupus erythematosus in Mexican population

article

Association of PDCD1 polymorphisms with childhood-onset systemic lupus erythematosus

artículo científico publicado en 2007

Association of TLR7 copy number variation with susceptibility to childhood-onset systemic lupus erythematosus in Mexican population

artículo científico publicado en 2010

Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice

artículo científico publicado en 2013

Bullous lesions as a manifestation of systemic lupus erythematosus in two Mexican teenagers

artículo científico publicado en 2010

Calidad de vida de los pacientes con inmunodeficiencias primarias de anticuerpos

Catastrophic Kawasaki disease or juvenile Polyarteritis nodosa?

artículo científico publicado en 2006

Characterization of Bruton's tyrosine kinase mutations in Mexican patients with X-linked agammaglobulinemia

artículo científico publicado en 2007

Clinical and genetic analysis of patients with X-linked hyper-IgM syndrome

article

Clinical and immunological features of common variable immunodeficiency in Mexican patients.

artículo científico publicado en 2013

Cochrane Review: Immunostimulants for preventing respiratory tract infection in children

Commentary on: ‘Immunostimulants for preventing respiratory tract infection in children’ with a response from the review authors

article

Common variable immunodeficiency. A clinical approach

artículo científico publicado en 2010

Consequences of two naturally occurring missense mutations in the structure and function of Bruton agammaglobulinemia tyrosine kinase

artículo científico publicado en 2012

Corticosteroid therapy for refractory infections in chronic granulomatous disease: case reports and review of the literature

artículo científico publicado en 2006

Critical issues and needs in management of primary immunodeficiency diseases in Latin America.

artículo científico publicado en 2010

Enfermedad de Kawasaki: cuadro clínico, exámenes de laboratorio y lesiones coronarias

Guidelines for the use of human immunoglobulin therapy in patients with primary immunodeficiencies in Latin America.

artículo científico

Hyper-IgE syndrome and autoimmunity in Mexican children

artículo científico publicado en 2006

IL-12Rβ1 deficiency: mutation update and description of the IL12RB1 variation database

artículo científico publicado en 2013

Immunogenicity of A 23-Valent Pneumococcal Polysaccharide Vaccine Among Mexican Children

Immunostimulants for preventing respiratory tract infection in children

artículo científico publicado en 2006

Increased pro-inflammatory cytokine production after lipopolysaccharide stimulation in patients with X-linked agammaglobulinemia.

artículo científico publicado en 2012

International Consensus Document (ICON): Common Variable Immunodeficiency Disorders

artículo científico publicado en 2016

Into Action: Improving Access to Optimum Care for all Primary Immunodeficiency Patients

artículo científico publicado en 2016

Juvenile rheumatoid arthritis and asthma, but not childhood-onset systemic lupus erythematosus are associated with FCRL3 polymorphisms in Mexicans

artículo científico publicado en 2012

Lymphocytes and B-cell abnormalities in patients with common variable immunodeficiency (CVID).

artículo científico publicado en 2013

Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with wiskott-Aldrich syndrome

artículo científico publicado en 2014

Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation

artículo científico publicado en 2013

Pediatric Churg-Strauss syndrome in Mexico

artículo científico publicado en 2006

Primary Immunodeficiency Diseases in Aguascalientes, Mexico: Results from an Educational Program

artículo científico publicado en 2016

Primary Immunodeficiency Diseases in Latin America: The Second Report of the LAGID Registry

scientific article published on 27 December 2006

Primary immunodeficiency diseases in Latin America: Proceedings of the Second Latin American Society for Immunodeficiencies (LASID) Advisory Board ⬇️

artículo científico publicado el 22 de febrero de 2011

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders

artículo científico publicado en 2016

Reply

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

artículo científico publicado en 2010

Search for poliovirus carriers among people with primary immune deficiency diseases in the United States, Mexico, Brazil, and the United Kingdom

artículo científico publicado en 2004

Survival of Mexican patients with paediatric-onset systemic lupus erythematosus and abnormal electroencephalogram

artículo científico publicado en 2012

Tumor necrosis factor-alpha is a common genetic risk factor for asthma, juvenile rheumatoid arthritis, and systemic lupus erythematosus in a Mexican pediatric population

artículo científico publicado en 2009

Lista de obras de Francisco Espinosa-Rosales

138 Transmission Pattern and Carriers Identification in Male Patients with Chronic Granulomatous Disease.

604 Phenotypic and Functional Analysis of B Cells in Patients with Common Variable Immunodeficiency.

A novel CD40LG deletion causes the hyper-IgM syndrome with normal CD40L expression in a 6-month-old child

Advances in primary immunodeficiency diseases in Latin America: epidemiology, research, and perspectives

Advancing the management of primary immunodeficiency diseases in Latin America: Latin American Society for Immunodeficiencies (LASID) Initiatives.

Association analysis of the PTPN22 gene in childhood-onset systemic lupus erythematosus in Mexican population

Association of PDCD1 polymorphisms with childhood-onset systemic lupus erythematosus

Association of TLR7 copy number variation with susceptibility to childhood-onset systemic lupus erythematosus in Mexican population

Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice

Bullous lesions as a manifestation of systemic lupus erythematosus in two Mexican teenagers

Calidad de vida de los pacientes con inmunodeficiencias primarias de anticuerpos

Catastrophic Kawasaki disease or juvenile Polyarteritis nodosa?

Characterization of Bruton's tyrosine kinase mutations in Mexican patients with X-linked agammaglobulinemia

Clinical and genetic analysis of patients with X-linked hyper-IgM syndrome

Clinical and immunological features of common variable immunodeficiency in Mexican patients.

Cochrane Review: Immunostimulants for preventing respiratory tract infection in children

Commentary on: ‘Immunostimulants for preventing respiratory tract infection in children’ with a response from the review authors

Common variable immunodeficiency. A clinical approach

Consequences of two naturally occurring missense mutations in the structure and function of Bruton agammaglobulinemia tyrosine kinase

Corticosteroid therapy for refractory infections in chronic granulomatous disease: case reports and review of the literature

Critical issues and needs in management of primary immunodeficiency diseases in Latin America.

Enfermedad de Kawasaki: cuadro clínico, exámenes de laboratorio y lesiones coronarias

Guidelines for the use of human immunoglobulin therapy in patients with primary immunodeficiencies in Latin America.

Hyper-IgE syndrome and autoimmunity in Mexican children

IL-12Rβ1 deficiency: mutation update and description of the IL12RB1 variation database

Immunogenicity of A 23-Valent Pneumococcal Polysaccharide Vaccine Among Mexican Children

Immunostimulants for preventing respiratory tract infection in children

Increased pro-inflammatory cytokine production after lipopolysaccharide stimulation in patients with X-linked agammaglobulinemia.

International Consensus Document (ICON): Common Variable Immunodeficiency Disorders

Into Action: Improving Access to Optimum Care for all Primary Immunodeficiency Patients

Juvenile rheumatoid arthritis and asthma, but not childhood-onset systemic lupus erythematosus are associated with FCRL3 polymorphisms in Mexicans

Lymphocytes and B-cell abnormalities in patients with common variable immunodeficiency (CVID).

Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with wiskott-Aldrich syndrome

Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation

Pediatric Churg-Strauss syndrome in Mexico

Primary Immunodeficiency Diseases in Aguascalientes, Mexico: Results from an Educational Program

Primary Immunodeficiency Diseases in Latin America: The Second Report of the LAGID Registry

Primary immunodeficiency diseases in Latin America: Proceedings of the Second Latin American Society for Immunodeficiencies (LASID) Advisory Board ⬇️

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders

Reply

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

Search for poliovirus carriers among people with primary immune deficiency diseases in the United States, Mexico, Brazil, and the United Kingdom

Survival of Mexican patients with paediatric-onset systemic lupus erythematosus and abnormal electroencephalogram

Tumor necrosis factor-alpha is a common genetic risk factor for asthma, juvenile rheumatoid arthritis, and systemic lupus erythematosus in a Mexican pediatric population

Use of corticosteroids as an alternative to surgical treatment for liver abscesses in chronic granulomatous disease