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Clinically Complex LRBA Deficiency Due to a Founder Allele in the Georgian Jewish Population.
Freund T, Baxter SK, Walsh T, Golan H, Kapelushnik J, Abramsohn-Goldenberg M, Benor S, Sarid N, Ram R, Alcalay Y, Segel R, Renbaum P, Stepensky P, King MC, Torgerson TR, Hagin D. Freund T, et al. Among authors: golan h. J Clin Immunol. 2023 Jan;43(1):151-164. doi: 10.1007/s10875-022-01358-7. Epub 2022 Sep 5. J Clin Immunol. 2023. PMID: 36063261
Sustained Response to Imatinib in a Pediatric Patient with Concurrent Myeloproliferative Disease and Lymphoblastic Lymphoma Associated with a CCDC88C-PDGFRB Fusion Gene.
Bielorai B, Leitner M, Goldstein G, Mehrian-Shai R, Trakhtenbrot L, Fisher T, Marcu V, Yalon M, Schiby G, Barel O, Cal N, Golan H, Toren A. Bielorai B, et al. Among authors: golan h. Acta Haematol. 2019;141(2):119-127. doi: 10.1159/000495687. Epub 2019 Feb 6. Acta Haematol. 2019. PMID: 30726835
Successful treatment of invasive aspergillosis in chronic granulomatous disease by granulocyte transfusions followed by peripheral blood stem cell transplantation.
Bielorai B, Toren A, Wolach B, Mandel M, Golan H, Neumann Y, Kaplinisky C, Weintraub M, Keller N, Amariglio N, Paswell J, Rechavi G. Bielorai B, et al. Among authors: golan h. Bone Marrow Transplant. 2000 Nov;26(9):1025-8. doi: 10.1038/sj.bmt.1702651. Bone Marrow Transplant. 2000. PMID: 11100285
152 results