First report on the Moroccan registry of primary immunodeficiencies: 15 years of experience (1998-2012) - Wikidata - wikimedia - TriplyDB

First report on the Moroccan registry of primary immunodeficiencies: 15 years of experience (1998-2012)

First report on the Moroccan registry of primary immunodeficiencies: 15 years of experience (1998-2012)

http://www.wikidata.org/entity/Q28235781

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Gene mutations responsible for primary immunodeficiency disorders: A report from the first primary immunodeficiency biobank in Iran Combined immunodeficiency in the United States and Kuwait: Comparison of patients' characteristics and molecular diagnosis.Primary Immunodeficiency Diseases in Highly Consanguineous Populations from Middle East and North Africa: Epidemiology, Diagnosis, and Care.CYBA encoding p22(phox), the cytochrome b558 alpha polypeptide: gene structure, expression, role and physiopathology.Family History of Early Infant Death Correlates with Earlier Age at Diagnosis But Not Shorter Time to Diagnosis for Severe Combined Immunodeficiency.[Clinical and immunological profile of 15 Moroccan patients with Hyper IgM syndrome].Primary Immunodeficiency Diseases in Oman: 10-Year Experience in a Tertiary Care Hospital.

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P2860

First report on the Moroccan registry of primary immunodeficiencies: 15 years of experience (1998-2012)

http://www.wikidata.org/entity/Q28235781

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2014 nî lūn-bûn

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2014年の論文

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P2860

Two Novel Frame Shift, Recurrent and De Novo Mutations in the ITGB2 (CD18) Gene Causing Leukocyte Adhesion Deficiency in a Highly Inbred North African Population.

Interleukin-12 receptor beta1 deficiency in a patient with abdominal tuberculosis

Population prevalence of diagnosed primary immunodeficiency diseases in the United States

Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency.

Incidence and temporal trends of primary immunodeficiency: a population-based cohort study

Primary immunodeficiencies in highly consanguineous North African populations.

Molecular defects in Moroccan patients with ataxia-telangiectasia.

The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population.

Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients.

Intermittent chronic neutropenia in a patient with familial Mediterranean fever.

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