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Year Number of Results
2013 2
2015 2
2016 4
2017 5
2018 4
2019 9
2020 8
2021 8
2022 18
2023 11
2024 6

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69 results

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PCDH19-clustering epilepsy, pathophysiology and clinical significance.
Kowkabi S, Yavarian M, Kaboodkhani R, Mohammadi M, Shervin Badv R. Kowkabi S, et al. Among authors: shervin badv r. Epilepsy Behav. 2024 Mar 22;154:109730. doi: 10.1016/j.yebeh.2024.109730. Online ahead of print. Epilepsy Behav. 2024. PMID: 38521028 Review.
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Ashrafi M, Kameli R, Hosseinpour S, Razmara E, Zamani Z, Rezaei Z, Mashayekhi R, Pak N, Barzegar M, Azizimalamiri R, Kashani MR, Khosroshahi N, Rasulinezhad M, Heidari M, Amanat M, Abdi A, Mohammadi B, Mohammadi M, Zamani GR, Badv RS, Omrani A, Nikbakht S, Bereshneh AH, Movahedinia M, Moghaddam HF, Ardakani HS, Akbari MG, Tousi MB, Shahi MV, Hosseini F, Amouzadeh MH, Hosseini SA, Nikkhah A, Khajeh A, Alizadeh H, Yarali B, Rohani M, Karimi P, Elahi HML, Hosseiny SMM, Sadeghzadeh MS, Mohebbi H, Moghadam MH, Aryan H, Vahidnezhad H, Soveizi M, Rabbani B, Rabbani A, Mahdieh N, Garshasbi M, Tavasoli AR. Ashrafi M, et al. Among authors: badv rs. Neurogenetics. 2023 Oct;24(4):279-289. doi: 10.1007/s10048-023-00730-y. Epub 2023 Aug 19. Neurogenetics. 2023. PMID: 37597066
COLQ-related congenital myasthenic syndrome: An integrative view.
Eshaghian T, Rabbani B, Badv RS, Mikaeeli S, Gharib B, Iyadurai S, Mahdieh N. Eshaghian T, et al. Among authors: badv rs. Neurogenetics. 2023 Jul;24(3):189-200. doi: 10.1007/s10048-023-00719-7. Epub 2023 May 25. Neurogenetics. 2023. PMID: 37231228
Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalities.
Whittle EF, Chilian M, Karimiani EG, Progri H, Buhas D, Kose M, Ganetzky RD, Toosi MB, Torbati PN, Badv RS, Shelihan I, Yang H, Elloumi HZ, Lee S, Jamshidi Y, Pittman AM, Houlden H, Ignatius E, Rahman S, Maroofian R, Yoon WH, Carroll CJ. Whittle EF, et al. Among authors: badv rs. Genet Med. 2023 Feb;25(2):100332. doi: 10.1016/j.gim.2022.11.001. Epub 2022 Dec 15. Genet Med. 2023. PMID: 36520152 Free PMC article.
Sexual Dimorphism in Telomere Length in Childhood Autism.
Panahi Y, Salasar Moghaddam F, Babaei K, Eftekhar M, Shervin Badv R, Eskandari MR, Vafaee-Shahi M, Pezeshk H, Pedram M. Panahi Y, et al. Among authors: shervin badv r. J Autism Dev Disord. 2023 May;53(5):2050-2061. doi: 10.1007/s10803-022-05486-2. Epub 2022 Feb 27. J Autism Dev Disord. 2023. PMID: 35220523
69 results