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Mutations of the RET-GDNF signaling pathway in Ondine's curse.
Amiel J, Salomon R, Attié T, Pelet A, Trang H, Mokhtari M, Gaultier C, Munnich A, Lyonnet S. Amiel J, et al. Among authors: mokhtari m. Am J Hum Genet. 1998 Mar;62(3):715-7. doi: 10.1086/301759. Am J Hum Genet. 1998. PMID: 9497256 Free PMC article. No abstract available.
Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes.
Richard P, Gaudon K, Andreux F, Yasaki E, Prioleau C, Bauché S, Barois A, Ioos C, Mayer M, Routon MC, Mokhtari M, Leroy JP, Fournier E, Hainque B, Koenig J, Fardeau M, Eymard B, Hantaï D. Richard P, et al. Among authors: mokhtari m. J Med Genet. 2003 Jun;40(6):e81. doi: 10.1136/jmg.40.6.e81. J Med Genet. 2003. PMID: 12807980 Free PMC article. No abstract available.
Evaluation of the COVID-19 vaccine effectiveness on the outcomes of COVID 19 disease in Iran: a test-negative case-control study.
Khosravi Shadmani F, Moradi G, Naghipour M, Torkaman Asadi F, Ahmadi A, Mirahmadizadeh A, Haghdoost AA, Mesgarpour B, Zahraei SM, Goya MM, Mokhtari M, Safari-Faramani R, Zomorrodi Zare F, Chegeni M, Najafi F. Khosravi Shadmani F, et al. Among authors: mokhtari m. Front Immunol. 2024 Aug 20;15:1420651. doi: 10.3389/fimmu.2024.1420651. eCollection 2024. Front Immunol. 2024. PMID: 39234259 Free PMC article.
551 results