Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome and recurrent intrauterine fetal death
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference4 articles.
1. Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome;Harbuz;Prenat Diagn,2010
2. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-related disorders: an evolving web of heritable autoimmune diseases;Verbsky;Curr Opin Pediatr,2013
3. Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity;Gambineri;J Allergy Clin Immunol,2008
4. Stillbirth rates: delivering estimates in 190 countries;Stanton;Lancet,2006
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1. The Landscape of Point Mutations in Human Protein Coding Genes Leading to Pregnancy Loss;International Journal of Molecular Sciences;2023-12-17
2. Gestational Development of the Human Immune System;Immunology and Allergy Clinics of North America;2023-02
3. A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops: a case report;BMC Medical Genomics;2021-02-26
4. Intrauterine IPEX;Frontiers in Pediatrics;2020-11-20
5. Clinical, Immunological, and Genetic Features in Patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) and IPEX-like Syndrome;The Journal of Allergy and Clinical Immunology: In Practice;2020-09
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