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Page 1
JAK2V617F Is a Risk Factor for TIA/Stroke in Young Patients.
Shapira Cohen T, Chodick G, Steinberg DM, Grossman E, Shohat M, Salomon O. Shapira Cohen T, et al. Among authors: shohat m. Thromb Haemost. 2022 Aug;122(8):1333-1340. doi: 10.1055/s-0042-1743470. Epub 2022 Mar 14. Thromb Haemost. 2022. PMID: 35288888
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.
Brownstein Z, Gulsuner S, Walsh T, Martins FTA, Taiber S, Isakov O, Lee MK, Bordeynik-Cohen M, Birkan M, Chang W, Casadei S, Danial-Farran N, Abu-Rayyan A, Carlson R, Kamal L, Arnthórsson AÖ, Sokolov M, Gilony D, Lipschitz N, Frydman M, Davidov B, Macarov M, Sagi M, Vinkler C, Poran H, Sharony R, Samra N, Zvi N, Baris-Feldman H, Singer A, Handzel O, Hertzano R, Ali-Naffaa D, Ruhrman-Shahar N, Madgar O, Sofrin-Drucker E, Peleg A, Khayat M, Shohat M, Basel-Salmon L, Pras E, Lev D, Wolf M, Steingrimsson E, Shomron N, Kelley MW, Kanaan MN, Allon-Shalev S, King MC, Avraham KB. Brownstein Z, et al. Among authors: shohat m. Clin Genet. 2020 Oct;98(4):353-364. doi: 10.1111/cge.13817. Epub 2020 Aug 24. Clin Genet. 2020. PMID: 33111345 Free PMC article.
Homozygous deletion of RAG1, RAG2 and 5' region TRAF6 causes severe immune suppression and atypical osteopetrosis.
Weisz Hubshman M, Basel-Vanagaite L, Krauss A, Konen O, Levy Y, Garty BZ, Smirin-Yosef P, Maya I, Lagovsky I, Taub E, Marom D, Gaash D, Shichrur K, Avigad S, Hayman-Manzur L, Villa A, Sobacchi C, Shohat M, Yaniv I, Stein J. Weisz Hubshman M, et al. Among authors: shohat m. Clin Genet. 2017 Jun;91(6):902-907. doi: 10.1111/cge.12916. Epub 2017 Mar 19. Clin Genet. 2017. PMID: 27808398
Abnormal liver test results in myotonic dystrophy.
Achiron A, Barak Y, Magal N, Shohat M, Cohen M, Barar R, Gadoth N. Achiron A, et al. Among authors: shohat m. J Clin Gastroenterol. 1998 Jun;26(4):292-5. doi: 10.1097/00004836-199806000-00016. J Clin Gastroenterol. 1998. PMID: 9649014
317 results