Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/article/10.1007/s00431-018-3248-1/fulltext.html
Reference48 articles.
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2. Agarwal S, Mayer L (2013) Diagnosis and treatment of gastrointestinal disorders in patients with primary immunodeficiency. Clin Gastroenterol Hepatol 11(9):1050–1063. https://doi.org/10.1016/j.cgh.2013.02.024
3. Aghamohammadi A, Abolhassani H, Biglari M, Abolmaali S, Moazzami K, Tabatabaeiyan M, Asgarian-Omran H, Parvaneh N, Mirahmadian M, Rezaei N (2011) Analysis of switched memory B cells in patients with IgA deficiency. Int Arch Allergy Immunol 156(4):462–468. https://doi.org/10.1159/000323903
4. Aghamohammadi A, Mohammadi J, Parvaneh N, Rezaei N, Moin M, Espanol T, Hammarstrom L (2008) Progression of selective IgA deficiency to common variable immunodeficiency. Int Arch Allergy Immunol 147:87–92. https://doi.org/10.1159/000135694
5. Aytekin C, Tuygun N, Gokce S, Dogu F, Ikinciogullari A (2012) Selective IgA deficiency: clinical and laboratory features of 118 children in Turkey. J Clin Immunol 32:961–966. https://doi.org/10.1007/s10875-012-9702-3
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