The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
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Activated PI3 Kinase Delta Syndrome: From Genetics to Therapy."Immune TOR-opathies," a Novel Disease Entity in Clinical Immunology.Transitional B Cells and TLR9 Responses Are Defective in Selective IgA Deficiency.Delayed Diagnosis and Complications of Predominantly Antibody Deficiencies in a Cohort of Australian Adults.The classification, genetic diagnosis and modelling of monogenic autoinflammatory disordersNeurological Manifestations of Primary ImmunodeficienciesThe Phenotype and Treatment of WIP Deficiency: Literature Synopsis and Review of a Patient With Pre-transplant Serial Donor Lymphocyte Infusions to Eliminate CMV
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The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年學術文章
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2017年學術文章
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name
The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
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The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
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type
label
The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
@en
The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
@nl
prefLabel
The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
@en
The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
@nl
P2093
P2860
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The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
@en
P2093
Amos Etzioni
Aziz Bousfiha
Capucine Picard
Charlotte Cunningham-Rundles
Christoph Klein
Eric Oksenhendler
Fatima Ailal
H Bobby Gaspar
Hans D Ochs
Jean-Laurent Casanova
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P2888
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10.1007/S10875-017-0465-8
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2017-12-11T00:00:00Z