Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood - Wikidata - awgldk - TriplyDB

Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood

Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood

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Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood

http://www.wikidata.org/entity/Q33429970

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2016 nî lūn-bûn

@nan

2016 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

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name

Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood

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Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood

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type

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Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood

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Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood

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Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood

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Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood

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FPED.2016.00003

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Frontiers in pediatrics

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Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood

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Sujal Ghosh

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Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity

Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations

Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations

Autoimmune and other cytopenias in primary immunodeficiencies: pathomechanisms, novel differential diagnoses, and treatment

Dominant-activating germline mutations in the gene encoding the PI(3)K catalytic subunit p110δ result in T cell senescence and human immunodeficiency

Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3.

The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis.

Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015.

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3

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scholarly article

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10.3389/FPED.2016.00003

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Markus G. Seidel

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2016-02-02T00:00:00Z

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292676234

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26870718

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