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Familial Emberger Syndrome With Autoimmunity, Hyper-Immunoglobulin E and Lymphatic Impairment Caused by a Novel GATA2 Mutation.
AlGassim M, Al Seraihi AF, AlShaibani A, Conca W, AlShehri S, Abouzied MM, Hamadah I, AlReshoodi S, Dasouki M, Sheikh F. AlGassim M, et al. Among authors: conca w. Hematol Oncol Stem Cell Ther. 2022 Jun 1;15(2):63-65. doi: 10.1016/j.hemonc.2020.05.004. Hematol Oncol Stem Cell Ther. 2022. PMID: 32497548 Free article. No abstract available.
An atypical pulmonary fibrosis is associated with co-inheritance of mutations in the calcium binding protein genes S100A3 and S100A13.
Al-Mutairy EA, Imtiaz FA, Khalid M, Al Qattan S, Saleh S, Mahmoud LM, Al-Saif MM, Al-Haj L, Al-Enazi A, AlJebreen AM, Mohammed SF, Mobeireek AF, Alkattan K, Chisti MA, Luzina IG, Al-Owain M, Weheba I, Abdelsayed AM, Ramzan K, Janssen LJ, Conca W, Alaiya A, Collison KS, Meyer BF, Atamas SP, Khabar KS, Hasday JD, Al-Mohanna F. Al-Mutairy EA, et al. Among authors: conca w. Eur Respir J. 2019 Jul 18;54(1):1802041. doi: 10.1183/13993003.02041-2018. Print 2019 Jul. Eur Respir J. 2019. PMID: 31073086 Free PMC article.
Pathophysiology of ANCA-associated Vasculitis.
Al-Hussain T, Hussein MH, Conca W, Al Mana H, Akhtar M. Al-Hussain T, et al. Among authors: conca w. Adv Anat Pathol. 2017 Jul;24(4):226-234. doi: 10.1097/PAP.0000000000000154. Adv Anat Pathol. 2017. PMID: 28537941 Review.
48 results