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Rosacea as a striking feature in family members with a STAT1 gain‐of‐function mutation

Journal of the European Academy of Dermatology and Venereology, 2020-06, Vol.34 (6), p.e265-e267

2020

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Molecular analysis for patients with IL-12 receptor β1 deficiency

Clinical genetics, 2014-08, Vol.86 (2), p.161-166

2014

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Recurrent Salmonella Infections and Nephritis Complicating IgA Vasculitis in a Patient with IL-12Rβ1 Deficiency

Journal of investigational allergology & clinical immunology, 2022-07, Vol.32 (4), p.308-310

2022

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Systemic Autoimmunity in a Patient With CANDLE Syndrome

Journal of investigational allergology & clinical immunology, 2019-02, Vol.29 (1), p.75-76

2019

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Pulmonary Geotrichosis in Chronic Granulomatous Disease

Journal of investigational allergology & clinical immunology, 2022-01, Vol.32 (4), p.306-308

2022

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Clinical Manifestations in Carriers of X-Linked Chronic Granulomatous Disease in Mexico

Journal of investigational allergology & clinical immunology, 2019-04, Vol.29 (2), p.134-136

2019

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Molecular analysis for patients with IL-12 receptor beta 1 deficiency

Clinical genetics, 2014-08, Vol.86 (2), p.161-166

2014

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B subset cells in patients with chronic granulomatous disease in a Mexican population

Allergologia et immunopathologia, 2019-07, Vol.47 (4), p.372-377

2019

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Clinical and immunological features of common variable immunodeficiency in Mexican patients

Allergologia et immunopathologia, 2014-05, Vol.42 (3), p.235-240

2014

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

Allergologia et immunopathologia, 2014-01, Vol.42 (1), p.35-43

2014

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Severe congenital neutropenia with a novel ELANE mutation in 2 Mexican patients

Journal of investigational allergology & clinical immunology, 2014, Vol.24 (4), p.267-268

2014

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

Allergologia et immunopathologia, 2013-03, Vol.41 (2), p.108-113

2013

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Detection of inheritance pattern in thirty-three Mexican males with chronic granulomatous disease through 123 dihydrorhodamine assay

Allergologia et immunopathologia, 2014-11, Vol.42 (6), p.580-585

2014

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Association between maternal perceptions and actual nutritional status for children in a study group in Mexico

Nutrición hospitalaria : organo oficial de la Sociedad Española de Nutrición Parenteral y Enteral, 2012, Vol.27 (1), p.209-212

2012

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Salmonella vertebral osteitis and sepsis in a girl with interferon gamma pathway deficiency

Journal of investigational allergology & clinical immunology, 2012, Vol.22 (4), p.289-291

2012

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SFRP-01 – Recherche expérimentale – Défaut héréditaire de CYBB et prédisposition mendélienne aux infections mycobactériennes

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2008-06, Vol.15 (5), p.1031-1031

2008

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Rosacea as a striking feature in family members with a STAT 1 gain‐of‐function mutation

Journal of the European Academy of Dermatology and Venereology, 2020-06, Vol.34 (6)

2020

Volltextzugriff (PDF)

Molecular analysis for patients with IL-12 receptor [beta]1 deficiency

Clinical genetics, 2014-08, Vol.86 (2), p.161

2014

Volltextzugriff (PDF)

Association between maternal perceptions and actual nutritional status for children in a study group in Mexico Asociación entre la percepción materna y el estado nutricional real de los niños en un grupo de estudio en México

Nutrición hospitalaria : organo oficial de la Sociedad Española de Nutrición Parenteral y Enteral, 2012-02, Vol.27 (1), p.209-212

2012

Volltextzugriff (PDF)

Rosacea as a striking feature in family members with a STAT1 gain-of-function mutation

Journal of the European Academy of Dermatology and Venereology : JEADV, 2020, Vol.34 (6), p.e265-e267

2020

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Successful adjunctive immunoglobulin treatment in patients affected by leukocyte adhesion deficiency type 1 (LAD-1)

Immunologic research, 2014-12, Vol.61 (3), p.260-268

2014

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Description of BCG and Tuberculosis Disease in a Cohort of 79 Patients with Chronic Granulomatous Disease

Journal of clinical immunology, 2024-12, Vol.44 (8), p.171, Article 171

2024

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Successful adjunctive immunoglobulin treatment in patients affected by leukocyte adhesion deficiency type 1 (LAD-1)

Immunologic research, 2015-03, Vol.61 (3), p.260-268

2015

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Rosacea as a striking feature in family members with a STAT1 gain‐of‐function mutation

Molecular analysis for patients with IL-12 receptor β1 deficiency

Recurrent Salmonella Infections and Nephritis Complicating IgA Vasculitis in a Patient with IL-12Rβ1 Deficiency

Systemic Autoimmunity in a Patient With CANDLE Syndrome

Pulmonary Geotrichosis in Chronic Granulomatous Disease

Clinical Manifestations in Carriers of X-Linked Chronic Granulomatous Disease in Mexico

Molecular analysis for patients with IL-12 receptor beta 1 deficiency

B subset cells in patients with chronic granulomatous disease in a Mexican population

Clinical and immunological features of common variable immunodeficiency in Mexican patients

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

Severe congenital neutropenia with a novel ELANE mutation in 2 Mexican patients

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

Detection of inheritance pattern in thirty-three Mexican males with chronic granulomatous disease through 123 dihydrorhodamine assay

Association between maternal perceptions and actual nutritional status for children in a study group in Mexico

Salmonella vertebral osteitis and sepsis in a girl with interferon gamma pathway deficiency

SFRP-01 – Recherche expérimentale – Défaut héréditaire de CYBB et prédisposition mendélienne aux infections mycobactériennes

Rosacea as a striking feature in family members with a STAT 1 gain‐of‐function mutation

Molecular analysis for patients with IL-12 receptor [beta]1 deficiency

Association between maternal perceptions and actual nutritional status for children in a study group in Mexico Asociación entre la percepción materna y el estado nutricional real de los niños en un grupo de estudio en México

Rosacea as a striking feature in family members with a STAT1 gain-of-function mutation

Successful adjunctive immunoglobulin treatment in patients affected by leukocyte adhesion deficiency type 1 (LAD-1)

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

Description of BCG and Tuberculosis Disease in a Cohort of 79 Patients with Chronic Granulomatous Disease

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

Successful adjunctive immunoglobulin treatment in patients affected by leukocyte adhesion deficiency type 1 (LAD-1)

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