Items where Author is "Alavi, A."

Article

Hashemi, S.S. and Zare-Abdollahi, D. and Bakhshandeh, M.K. and Vafaee, A. and Abolhasani, S. and Inanloo Rahatloo, K. and DanaeeFard, F. and Farboodi, N. and Rohani, M. and Alavi, A. (2021) Clinical spectrum in multiple families with primary COQ10 deficiency. American Journal of Medical Genetics, Part A, 185 (2). pp. 440-452.

Haeri, G. and Hajiakhoundi, F. and Alavi, A. and Ghiasi, M. and Munhoz, R.P. and Rohani, M. (2021) Congenital Ichthyosis in a Case of Spinocerebellar Ataxia Type 34: A Novel Presentation for a Known Mutation. Movement Disorders Clinical Practice, 8 (2). pp. 275-278.

Khani, M. and Shamshiri, H. and Fatehi, F. and Rohani, M. and Haghi Ashtiani, B. and Akhoundi, F.H. and Alavi, A. and Moazzeni, H. and Taheri, H. and Ghani, M.T. and Javanparast, L. and Hashemi, S.S. and Haji-Seyed-Javadi, R. and Heidari, M. and Nafissi, S. and Elahi, E. (2020) Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations. Molecular Genetics and Genomic Medicine, 8 (7).

Haeri, G. and Akhoundi, F.H. and Alavi, A. and Abdi, S. and Rohani, M. (2020) Endocrine Abnormalities in a Case of Neurodegeneration with Brain Iron Accumulation. Movement Disorders Clinical Practice, 7 (6). pp. 706-707.

Rohani, M. and Fasano, A. and Akhoundi, F.H. and Haeri, G. and Lang, A.E. and Rahimi Bidgoli, M.M. and Javanparast, L. and Zamani, B. and Shahidi, G. and Alavi, A. (2019) Beta-propeller protein associated neurodegeneration (BPAN); the first report of three patients from Iran with de novo novel mutations. Parkinsonism and Related Disorders, 61. pp. 231-233.

Khani, M. and Alavi, A. and Shamshiri, H. and Zamani, B. and Hassanpour, H. and Kazemi, M.H. and Nafissi, S. and Elahi, E. (2019) Mutation screening of SLC52A3, C19orf12, and TARDBP in Iranian ALS patients. Neurobiology of Aging, 75. 225.e9-225.e14.

Rohani, M. and Fasano, A. and Lang, A.E. and Zamani, B. and Javanparast, L. and Bidgoli, M.-M.R. and Alavi, A. (2018) Pantothenate kinase-associated neurodegeneration mimicking Tourette syndrome: a case report and review of the literature. Neurological Sciences. pp. 1-4.

Rohani, M. and Fasano, A. and Lang, A.E. and Zamani, B. and Javanparast, L. and Bidgoli, M.-M.R. and Alavi, A. (2018) Pantothenate kinase-associated neurodegeneration mimicking Tourette syndrome: a case report and review of the literature. Neurological Sciences, 39 (10). pp. 1797-1800.

Mohammadi, M.R. and Ahmadi, N. and Salmanian, M. and Asadian-Koohestani, F. and Ghanizadeh, A. and Alavi, A. and Malek, A. and Dastgiri, S. and Moharreri, F. and Hebrani, P. and Arman, S. and Dastjerdi, J.K. and Motavallian, A. (2016) Psychiatric disorders in Iranian children and adolescents. Iranian Journal of Psychiatry, 11 (2). pp. 87-98.

Mohammadi, M.R. and Ahmadi, N. and Salmanian, M. and Asadian-Koohestani, F. and Ghanizadeh, A. and Alavi, A. and Malek, A. and Dastgiri, S. and Moharreri, F. and Hebrani, P. and Arman, S. and Dastjerdi, J.K. and Motavallian, A. (2016) Psychiatric disorders in Iranian children and adolescents. Iranian Journal of Psychiatry, 11 (2). pp. 87-98.

Mohammadi, M.R. and Salmanian, M. and Ghanizadeh, A. and Alavi, A. and Malek, A. and Fathzadeh, H. and Moharreri, F. and Hebrani, P. and Arman, S. and Khoshhal Dastjerdi, J. and Motavallian, A. (2014) Psychological problems of Iranian children and adolescents: Parent report form of Strengths and Difficulties Questionnaire. Journal of Mental Health, 23 (6). pp. 287-291.