The First Purine Nucleoside Phosphorylase Deficiency Patient Resembling IgA Deficiency and a Review of the Literature-Reference-Cited by-同舟云学术

The First Purine Nucleoside Phosphorylase Deficiency Patient Resembling IgA Deficiency and a Review of the Literature

Published:2019-03-19 Issue:4 Volume:48 Page:410-430
ISSN:0882-0139
Container-title:Immunological Investigations
language:en
Short-container-title:Immunological Investigations

Author:

Fekrvand Saba¹^ORCID,Yazdani Reza¹,Abolhassani Hassan¹²,Ghaffari Javad³,Aghamohammadi Asghar¹

Affiliation:

1. Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children’s Medical Center, Tehran, and the University of Medical Science, Tehran, Iran

2. Division of Clinical Immunology, Department of Laboratory Medicine, Karolinska Institute at Karolinska University Hospital Huddinge, Stockholm, Sweden

3. Department of Pediatrics, Mazandaran University of Medical Sciences, Sari, Iran

Publisher

Informa UK Limited

Subject

General Medicine,Immunology

Link

https://www.tandfonline.com/doi/pdf/10.1080/08820139.2019.1570249

Reference82 articles.

1. Clinical implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency

2. Purine nucleoside phosphorylase deficiency in two unrelated Saudi patients

3. A novel mutation in purine nucleoside phosphorylase in a child with normal uric acid levels

4. Early Immune Response in Healthy and Immunocompromised Subjects with Primary Varicella-Zoster Virus Infection

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