Clinical, immunological features and follow up of 20 patients with dedicator of cytokinesis 8 (DOCK8) deficiency-Reference-Cited by-同舟云学术

Clinical, immunological features and follow up of 20 patients with dedicator of cytokinesis 8 (DOCK8) deficiency

Published:2020-03-11 Issue:5 Volume:31 Page:515-527
ISSN:0905-6157
Container-title:Pediatric Allergy and Immunology
language:en
Short-container-title:Pediatr Allergy Immunol

Author:

Haskologlu Sule¹^ORCID,Kostel Bal Sevgi¹,Islamoglu Candan¹,Aytekin Caner²,Guner Sukru³,Sevinc Selin¹,Keles Sevgi³,Kendirli Tanil⁴,Ceylaner Serdar⁵,Dogu Figen¹,Ikinciogullari Aydan¹

Affiliation:

1. Department of Pediatrics Division of Immunology and Allergy Ankara University Faculty of Medicine Ankara Turkey

2. Department of Pediatric Immunology Dr.Sami Ulus Maternity and Children’s Health and Diseases Training and Research Hospital Ankara Turkey

3. Department of Pediatrics Division of Immunology and Allergy Necmettin Erbakan University Faculty of Medicine Konya Turkey

4. Pediatric Intensive Care Unit Ankara University School of Medicine Ankara Turkey

5. Intergen Genetic Diagnosis Center Ankara Turkey

Publisher

Wiley

Subject

Immunology,Immunology and Allergy,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pai.13236

Reference27 articles.

1. Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity

2. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome

3. Combined Immunodeficiency Associated withDOCK8Mutations

4. Dedicator of cytokinesis 8 (DOCK8) deficiency

5. DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A novel hemizygous CD40L mutation of X-linked hyper IgM syndromes and compound heterozygous DOCK8 mutations of hyper IgE syndromes in two Chinese families;Immunogenetics;2024-04-08

2. Clinical, immunological, and genetic description of a Mexican cohort of patients with DOCK8 deficiency;Pediatric Allergy and Immunology;2024-02

3. Reduced toxicity conditioning and a high CD34+ cell dose can achieve full donor chimerism in DOCK8 deficiency;Journal of Allergy and Clinical Immunology: Global;2023-08

4. Successful treatment of DOCK8 deficiency by allogeneic hematopoietic cell transplantation from alternative donors;International Journal of Hematology;2023-05-03

5. Genetics of Inborn Errors of Immunity in highly consanguineous Middle Eastern and North African populations;Seminars in Immunology;2023-05