WHIM syndrome: congenital immune deficiency disease
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology
Reference58 articles.
1. A new familial immunodeficiency disorder characterized by severe neutropenia, a defective marrow release mechanism, and hypogammaglobulinemia
2. Myelokathexis — A New Form of Chronic Granulocytopenia
3. WHIM syndrome, an autosomal dominant disorder: Clinical, hematological, and molecular studies
4. Role of the intracellular domains of CXCR4 in SDF-1–mediated signaling
5. Myelokathexis: a rare form of chronic benign granulocytopenia
Cited by 183 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. Periodontal disease in patients with WHIM syndrome;Journal of Clinical Periodontology;2024-01-07
2. Congenital neutropenia: From lab bench to clinic bedside and back;Mutation Research/Reviews in Mutation Research;2024-01
3. Increased Susceptibility of WHIM Mice to Papillomavirus-induced Disease is Dependent upon Immune Cell Dysfunction;2023-11-15
4. WHIM Syndrome: Report of a Novel Familial CXCR4V340fs Gain-of-function Mutation with a Milder Phenotype;2023-11-14
5. Nature and nurture: understanding phenotypic variation in inborn errors of immunity;Frontiers in Cellular and Infection Microbiology;2023-09-14
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