Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Notes: The journal of allergy and clinical immunology. - 141, 6 (2018) , 2303-2306, ISSN: 1097-6825

Event: Veröffentlichung

(where): Freiburg

(who): Universität

(when): 2021

Creator: Lawless, Dylan
Geier, Christoph B.
Ehl, Stephan
Speckmann, Carsten
Walter, Jolan E.
Savic, Sinisa

DOI: 10.1016/j.jaci.2018.02.007

URN: urn:nbn:de:bsz:25-freidok-1758465

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 25.03.2025, 1:46 PM CET

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Associated

Lawless, Dylan
Geier, Christoph B.
Ehl, Stephan
Speckmann, Carsten
Walter, Jolan E.
Savic, Sinisa
Universität

Time of origin

2021

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Rolle des Recombination Activating Gene 1 (RAG 1) im ventrikulären Remodeling nach Myokardinfarkt

Confirmation of the localization of the human recombination activating gene 1 (RAG1) to chromosome 11p13

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DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency

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Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate kinase deficiency natural history study

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Rolle des Recombination Activating Gene 1 (RAG 1) im ventrikulären Remodeling nach Myokardinfarkt

Confirmation of the localization of the human recombination activating gene 1 (RAG1) to chromosome 11p13

MAP kinase activating death domain deficiency is a novel cause of impaired lymphocyte cytotoxicity

Severe plasma prekallikrein deficiency: clinical characteristics, novel KLKB1 mutations, and estimated prevalence

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Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate kinase deficiency natural history study

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Common Variable Immunodeficiency

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Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency

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Other Objects (12)

BCL10 deficiency presenting as severe combined immunodeficiency escaping newborn screening

Rolle des Recombination Activating Gene 1 (RAG 1) im ventrikulären Remodeling nach Myokardinfarkt

Confirmation of the localization of the human recombination activating gene 1 (RAG1) to chromosome 11p13

MAP kinase activating death domain deficiency is a novel cause of impaired lymphocyte cytotoxicity

Severe plasma prekallikrein deficiency: clinical characteristics, novel KLKB1 mutations, and estimated prevalence

Severe plasma prekallikrein deficiency : clinical characteristics, novel KLKB1 mutations, and estimated prevalence

Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis

DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency

Base composition, selection, and phylogenetic significance of indels in the recombination activating gene-1 in vertebrates

Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate kinase deficiency natural history study

Common Variable Immunodeficiency

Acquired immunodeficiency syndrome

BCL10 deficiency presenting as severe combined immunodeficiency escaping newborn screening

Rolle des Recombination Activating Gene 1 (RAG 1) im ventrikulären Remodeling nach Myokardinfarkt

Confirmation of the localization of the human recombination activating gene 1 (RAG1) to chromosome 11p13

MAP kinase activating death domain deficiency is a novel cause of impaired lymphocyte cytotoxicity

Severe plasma prekallikrein deficiency: clinical characteristics, novel KLKB1 mutations, and estimated prevalence

Severe plasma prekallikrein deficiency : clinical characteristics, novel KLKB1 mutations, and estimated prevalence

Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis

DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency

Base composition, selection, and phylogenetic significance of indels in the recombination activating gene-1 in vertebrates

Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate kinase deficiency natural history study

Common Variable Immunodeficiency

Acquired immunodeficiency syndrome

BCL10 deficiency presenting as severe combined immunodeficiency escaping newborn screening

Rolle des Recombination Activating Gene 1 (RAG 1) im ventrikulären Remodeling nach Myokardinfarkt

Confirmation of the localization of the human recombination activating gene 1 (RAG1) to chromosome 11p13

MAP kinase activating death domain deficiency is a novel cause of impaired lymphocyte cytotoxicity

Severe plasma prekallikrein deficiency: clinical characteristics, novel KLKB1 mutations, and estimated prevalence

Severe plasma prekallikrein deficiency : clinical characteristics, novel KLKB1 mutations, and estimated prevalence

Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis

DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency

Base composition, selection, and phylogenetic significance of indels in the recombination activating gene-1 in vertebrates

Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate kinase deficiency natural history study

Common Variable Immunodeficiency

Acquired immunodeficiency syndrome

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