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Heshmatzad, K. and Haghi Panah, M. and Tavasoli, A.R. and Ashrafi, M.R. and Mahdieh, N. and Rabbani, B. (2021) GFAP variants leading to infantile Alexander disease: Phenotype and genotype analysis of 135 cases and report of a de novo variant. Clinical Neurology and Neurosurgery, 207.
Mahdieh, N. and Soveizi, M. and Tavasoli, A.R. and Rabbani, A. and Ashrafi, M.R. and Kohlschütter, A. and Rabbani, B. (2021) Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants. Scientific Reports, 11 (1).
Mohammadi, P. and Daneshmand, M.A. and Mahdieh, N. and Ashrafi, M.R. and Heidari, M. and Garshasbi, M. (2021) Identification of a novel missense c.386G > A variant in a boy with the POMGNT1-related muscular dystrophy-dystroglycanopathy. Acta Neurologica Belgica, 121 (1). pp. 143-151.
Ashrafi, M.R. and Azizimalamiri, R. and Badv, R.S. and Tavasoli, A.R. and Nikkhah, A. and Montazerlotfelahi, H. and Vafaee-Shahi, M. and Heidari, M. (2020) Coronavirus, its neurologic manifestations, and complications. Iranian Journal of Pediatrics, 30 (2). pp. 1-4.
Rezaei, Z. and Hosseinpour, S. and Ashrafi, M.R. and Mahdieh, N. and Alizadeh, H. and Mohammadpour, M. and Khosroshahi, N. and Amanat, M. and Tavasoli, A.R. (2019) Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated Patients. Neuropediatrics, 50 (2). pp. 130-134.
