Inheritance pattern and clinical aspects of 93 Iranian patients with chronic granulomatous disease. - Wikidata - wikimedia - TriplyDB

Inheritance pattern and clinical aspects of 93 Iranian patients with chronic granulomatous disease.

Inheritance pattern and clinical aspects of 93 Iranian patients with chronic granulomatous disease.

http://www.wikidata.org/entity/Q47854983

about

Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity Bacillus Calmette-Guérin (BCG) complications associated with primary immunodeficiency diseases Clinical Features and Genetic Analysis of 48 Patients with Chronic Granulomatous Disease in a Single Center Study from Shanghai, China (2005-2015): New Studies and a Literature Review.Genetics of consanguinity and inbreeding in health and disease.Bacillus calmette-guerin infection in NADPH oxidase deficiency: defective mycobacterial sequestration and granuloma formation.Phagocyte NADPH oxidase, chronic granulomatous disease and mycobacterial infections.Common severe infections in chronic granulomatous disease Necrotizing Liver Granuloma/Abscess and Constrictive Aspergillosis Pericarditis with Central Nervous System Involvement: Different Remarkable Phenotypes in Different Chronic Granulomatous Disease Genotypes.Infections associated with chronic granulomatous disease: linking genetics to phenotypic expression.Pulmonary manifestations of chronic granulomatous disease.Phagocyte NADPH oxidase and specific immunity.Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects.Staphylococcus aureus, phagocyte NADPH oxidase and chronic granulomatous disease.Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.Infection Profile in Chronic Granulomatous Disease: a 23-Year Experience from a Tertiary Care Center in North India.Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients.A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients.Three novel mutations in CYBA among 22 Iranians with Chronic granulomatous disease.Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindreds.A Review of Chronic Granulomatous Disease.The three CYBA variants (rs4673, rs1049254 and rs1049255) are benign: new evidence from a patient with CGD.Aspergillosis in Chronic Granulomatous Disease.Paecilomyces formosus Infection in an Adult Patient with Undiagnosed Chronic Granulomatous Disease.NADPH Oxidase Deficiency: A Multisystem Approach.Considerations in the Diagnosis of Chronic Granulomatous Disease.

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P2860

Inheritance pattern and clinical aspects of 93 Iranian patients with chronic granulomatous disease.

http://www.wikidata.org/entity/Q47854983

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2011 nî lūn-bûn

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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Inheritance pattern and clinic ...... chronic granulomatous disease.

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Inheritance pattern and clinic ...... chronic granulomatous disease.

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Inheritance pattern and clinic ...... chronic granulomatous disease.

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Inheritance pattern and clinic ...... chronic granulomatous disease.

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Inheritance pattern and clinic ...... chronic granulomatous disease.

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Journal of Clinical Immunology

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Inheritance pattern and clinic ...... chronic granulomatous disease.

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Fariborz Zandieh

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Fatemeh Behmanesh

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Ghamar Taj Khotaei

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Iraj Mohammadzadeh

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Leyla Sedighipour

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Masoud Movahedi

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Mohammad Hassan Bemanian

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Mohsen Badalzadeh

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Mostafa Moin

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P2860

Chronic granulomatous disease: the European experience

Special article: chronic granulomatous disease in the United Kingdom and Ireland: a comprehensive national patient-based registry

Follow up of patients with chronic granulomatous disease diagnosed since 1990

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)

Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia

First report of clinical, functional, and molecular investigation of chronic granulomatous disease in nine Jordanian families

Genetic, biochemical, and clinical features of chronic granulomatous disease.

Genetic referrals of Middle Eastern origin in a western city: inbreeding and disease profile.

Chronic granulomatous disease. Report on a national registry of 368 patients.

Consanguinity and its relevance to clinical genetics.

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Mohammad Reza Fazlollahi

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