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A Rare Case of Cerebrotendinous Xanthomatosis Associated With a Mutation on COG8 Gene.
J Investig Med High Impact Case Rep. 2023 Jan-Dec;11:23247096231168109. doi: 10.1177/23247096231168109.
J Investig Med High Impact Case Rep. 2023.
PMID: 37083278
Free PMC article.
A novel variant of Paganini-Miozzo syndrome: a case report.
Sarmadian R, Gilani A, Biglari HN.
Sarmadian R, et al. Among authors: biglari hn.
Oxf Med Case Reports. 2023 Mar 25;2023(3):omad024. doi: 10.1093/omcr/omad024. eCollection 2023 Mar.
Oxf Med Case Reports. 2023.
PMID: 36993824
Free PMC article.
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An unusual case of a toddler with Canavan disease with frequent intractable seizures: A case report and review of the literature.
Irilouzadian R, Goudarzi A, Hesami H, Sarmadian R, Biglari HN, Gilani A.
Irilouzadian R, et al. Among authors: biglari hn.
SAGE Open Med Case Rep. 2023 Mar 21;11:2050313X231160885. doi: 10.1177/2050313X231160885. eCollection 2023.
SAGE Open Med Case Rep. 2023.
PMID: 36968992
Free PMC article.
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The First Report of Iranian Registry of Patients with Spinal Muscular Atrophy.
Mansouri V, Heidari M, Bemanalizadeh M, Azizimalamiri R, Nafissi S, Akbari MG, Barzegar M, Moayedi AR, Badv RS, Mohamadi M, Tavasoli AR, Amirsalari S, Khajeh A, Inaloo S, Fatehi F, Hosseinpour S, Babaei M, Hosseini SA, Mahdi Hosseiny SM, Fayyazi A, Hosseini F, Toosi MB, Khosroshahi N, Ghabeli H, Biglari HN, Kakhki SK, Mirlohi SH, Bidabadi E, Mohammadi B, Omrani A, Sedighi M, Vafaee-Shahi M, Rasulinezhad M, Hoseini SM, Movahedinia M, Rezaei Z, Karimi P, Farshadmoghadam H, Anvari S, Yaghini O, Nasiri J, Zamani G, Ashrafi MR.
Mansouri V, et al. Among authors: biglari hn.
J Neuromuscul Dis. 2023;10(2):211-225. doi: 10.3233/JND-221614.
J Neuromuscul Dis. 2023.
PMID: 36776076
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