A Case Series of Adenosine Deaminase 2-deficient Patients Emphasizing Treatment and Genotype-phenotype Correlations-Reference-Cited by-同舟云学术

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A Case Series of Adenosine Deaminase 2-deficient Patients Emphasizing Treatment and Genotype-phenotype Correlations

Published:2015-08 Issue:8 Volume:42 Page:1532-1534
ISSN:0315-162X
Container-title:The Journal of Rheumatology
language:en
Short-container-title:J Rheumatol

Author:

BATU EZGI DENIZ,KARADAG OMER,TASKIRAN EKIM ZIHNI,KALYONCU UMUT,AKSENTIJEVICH IVONA,ALIKASIFOGLU MEHMET,ÖZEN SEZA

Publisher

The Journal of Rheumatology

Subject

Immunology,Immunology and Allergy,Rheumatology

Reference12 articles.

1. Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy

2. Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2

3. Novel adenosine deaminase 2 mutations in a child with a fatal vasculopathy

4. 2012 Revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides

5. The American College of Rheumatology 1990 criteria for the classification of polyarteritis nodosa;Lightfoot;Arthritis Rheum,1990

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1. ADA2 Eksikliği;Güncel Pediatri;2024-08-15

2. Deficiency of adenosine deaminase type 2 (DADA2): clinical picture, diagnosis and treatment;Vnitřní lékařství;2024-06-20

3. Central retinal artery occlusion in a child with ADA2 deficiency: a case report;Annals of Medicine & Surgery;2024-02-28

4. Vasculitis and vasculopathy associated with inborn errors of immunity: an overview;Frontiers in Pediatrics;2024-01-31

5. Neurological involvement in patients with primary immunodeficiency;Allergologia et Immunopathologia;2024-01-01

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