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Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes.
Darvish H, Azcona LJ, Tafakhori A, Mesias R, Ahmadifard A, Sanchez E, Habibi A, Alehabib E, Johari AH, Emamalizadeh B, Jamali F, Chapi M, Jamshidi J, Kajiwara Y, Paisán-Ruiz C. Darvish H, et al. Among authors: jamali f. Sci Rep. 2020 Jan 22;10(1):968. doi: 10.1038/s41598-020-57929-4. Sci Rep. 2020. PMID: 31969655 Free PMC article.
Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy.
Chapi M, Sabbaghi H, Suri F, Alehabib E, Rahimi-Aliabadi S, Jamali F, Jamshidi J, Emamalizadeh B, Darvish H, Mirrahimi M, Ahmadieh H, Daftarian N. Chapi M, et al. Among authors: jamali f. Ophthalmic Genet. 2019 Jun;40(3):259-266. doi: 10.1080/13816810.2019.1622023. Epub 2019 Jun 19. Ophthalmic Genet. 2019. PMID: 31215831
Treatment of Myoclonus-dystonia with carbamazepine.
Sanjari Moghaddam H, Tafakhori A, Darvish H, Mahmoudi-Gharaei J, Jamali F, Aghamollaii V. Sanjari Moghaddam H, et al. Among authors: jamali f. Parkinsonism Relat Disord. 2018 Aug;53:116-117. doi: 10.1016/j.parkreldis.2018.05.005. Epub 2018 May 28. Parkinsonism Relat Disord. 2018. PMID: 29853296 No abstract available.
341 results