Items where Author is "Rohani, M."

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Number of items: 26.

Article

Azimi, A. and Parvaresh, M. and Shahidi, G. and Habibi, A. and Rohani, S. and Safdarian, M. and Fattahi, A. and Taheri, M. and Rohani, M. (2018) Anteromedial GPi deep brain stimulation in Tourette syndrome: The first case series from Iran. Clinical Neurology and Neurosurgery, 172. pp. 116-119.

Mostafavi, E. and Ghasemi, A. and Rohani, M. and Molaeipoor, L. and Esmaeili, S. and Mohammadi, Z. and Mahmoudi, A. and Aliabadian, M. and Johansson, A. (2018) Molecular survey of tularemia and plague in small mammals from Iran. Frontiers in Cellular and Infection Microbiology, 8 (JUL).

Khajevand-Khazaei, M.-R. and Ziaee, P. and Motevalizadeh, S.-A. and Rohani, M. and Afshin-Majd, S. and Baluchnejadmojarad, T. and Roghani, M. (2018) Naringenin ameliorates learning and memory impairment following systemic lipopolysaccharide challenge in the rat. European Journal of Pharmacology, 826. pp. 114-122.

Khajevand-Khazaei, M.-R. and Ziaee, P. and Motevalizadeh, S.-A. and Rohani, M. and Afshin-Majd, S. and Baluchnejadmojarad, T. and Roghani, M. (2018) Naringenin ameliorates learning and memory impairment following systemic lipopolysaccharide challenge in the rat. European Journal of Pharmacology, 826. pp. 114-122.

Rohani, M. and Shahidi, G. and Vali, F. and Lang, A.E. and Slow, E. and Gahl, W.A. and Behnam, B. (2018) Oculogyric crises in PLA2G6 associated neurodegeneration. Parkinsonism and Related Disorders, 52. pp. 111-112.

Rohani, M. and Shahidi, G. and Vali, F. and Lang, A.E. and Slow, E. and Gahl, W.A. and Behnam, B. (2018) Oculogyric crises in PLA2G6 associated neurodegeneration. Parkinsonism and Related Disorders, 52. pp. 111-112.

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.

Rohani, M. and Meysamie, A. and Zamani, B. and Sowlat, M.M. and Akhoundi, F.H. (2018) Reduced retinal nerve fiber layer (RNFL) thickness in ALS patients: a window to disease progression. Journal of Neurology, 265 (7). pp. 1557-1562.

Shahidi, G. and Rohani, M. and Munhoz, R.P. and Akhoundi, F.H. (2018) Tardive akathisia with asymmetric and upper-body presentation: Report of two cases and literature review. Tremor and Other Hyperkinetic Movements, 8.

Rohani, M. and Munhoz, R.P. and Haeri, G. (2017) Abnormal movements induced by methanol toxicity. Postgraduate Medical Journal, 93 (1106). e2.

Rohani, M. and Mohseni, M. and Arami, M. and Rezazadeh, A. (2017) Palatal tremor with audible click. Postgraduate Medical Journal, 93 (1106). e1.

Safdarian, M. and Munhoz, R.P. and Aghaei, M. and Rohani, M. (2017) Wilson�s disease presenting as central pontine myelinolysis. Neurological Sciences, 38 (12). pp. 2223-2225.

Safdarian, M. and Munhoz, R.P. and Aghaei, M. and Rohani, M. (2017) Wilson�s disease presenting as central pontine myelinolysis. Neurological Sciences, 38 (12). pp. 2223-2225.

Fallahi, B. and Esmaeili, A. and Beiki, D. and Oveisgharan, S. and Noorollahi-Moghaddam, H. and Erfani, M. and Tafakhori, A. and Rohani, M. and Fard-Esfahani, A. and Emami-Ardekani, A. and Geramifar, P. and Eftekhari, M. (2016) Evaluation of 99mTc-TRODAT-1 SPECT in the diagnosis of Parkinson�s disease versus other progressive movement disorders. Annals of Nuclear Medicine, 30 (2). pp. 153-162.

Noohi, N. and Ebrahimipour, G. and Rohani, M. and Talebi, M. and Pourshafie, M.R. (2016) Evaluation of potential probiotic characteristics and antibacterial effects of strains of Pediococcus species isolated from broiler chickens. British Poultry Science, 57 (3). pp. 317-323.

Rohani, M. and Almasi, M. and Soltan Sanjari, M. (2016) Familial Horizontal Gaze Palsy With Progressive Scoliosis. Pediatric Neurology, 64. pp. 103-104.

Jaberi, E. and Rohani, M. and Shahidi, G.A. and Nafissi, S. and Arefian, E. and Soleimani, M. and Rasooli, P. and Ahmadieh, H. and Daftarian, N. and KaramiNejadRanjbar, M. and Klotzle, B. and Fan, J.-B. and Turk, C. and Steemers, F. and Elahi, E. (2016) Identification of mutation in GTPBP2 in patients of a family with neurodegeneration accompanied by iron deposition in the brain. Neurobiology of Aging, 38. 216.e11-216.e18.

Jaberi, E. and Rohani, M. and Shahidi, G.A. and Nafissi, S. and Arefian, E. and Soleimani, M. and Moghadam, A. and Arzenani, M.K. and Keramatian, F. and Klotzle, B. and Fan, J.-B. and Turk, C. and Steemers, F. and Elahi, E. (2016) Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction. Movement Disorders, 31 (7). pp. 1004-1011.

Rohani, M. and Almasi, M. (2016) Supranuclear gaze palsy and hummingbird sign. Postgraduate Medical Journal, 92 (1094). p. 743.

Shamshiri, H. and Fatehi, F. and Davoudi, F. and Mir, E. and Pourmirza, B. and Abolfazli, R. and Etemadifar, M. and Harirchian, M.H. and Gharagozli, K. and Ayromlou, H. and Basiri, K. and Zamani, B. and Rohani, M. and Sedighi, B. and Roudbari, A. and Delavar Kasmaei, H. and Nikkhah, K. and Ranjbar Naeini, A. and Nafissi, S. (2015) Amyotrophic lateral sclerosis progression: Iran-ALS clinical registry, a multicentre study. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 16 (7-8). pp. 506-511.

Rohani, M. and Noohi, N. and Talebi, M. and Katouli, M. and Pourshafie, M.R. (2015) Highly heterogeneous probiotic Lactobacillus species in healthy iranians with low functional activities. PLoS ONE, 10 (12).

Jaberi, E. and Rohani, M. and Shahidi, G.A. and Nafissi, S. and Arefian, E. and Soleimani, M. and Rasooli, P. and Ahmadieh, H. and Daftarian, N. and KaramiNejadRanjbar, M. and Klotzle, B. and Fan, J.-B. and Turk, C. and Steemers, F. and Elahi, E. (2015) Identification of mutation in GTPBP2 in patients of a family with neurodegeneration accompanied by iron deposition in the brain. Neurobiology of Aging, 38. 216.e11-216.e18.

Rohani, M. and Aghaei, M. and Jenabi, A. and Yazdanfar, S. and Mousavi, D. and Miri, S. (2015) Restless legs syndrome in hemodialysis patients in Iran. Neurological Sciences, 36 (5). pp. 723-727.

Rohani, M. and Miri, S. (2015) Teaching Video NeuroImages: Hand tremor, tongue and perioral fasciculation in a patient with Kennedy disease. Neurology, 84 (10). e76.

Ghazavi, F. and Fazlali, Z. and Banihosseini, S.S. and Hosseini, S.-R. and Kazemi, M.H. and Shojaee, S. and Parsa, K. and Sadeghi, H. and Sina, F. and Rohani, M. and Shahidi, G.-A. and Ghaemi, N. and Ronaghi, M. and Elahi, E. (2011) PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutations. Movement Disorders, 26 (1). pp. 80-89.

This list was generated on Sun Sep 22 08:11:20 2019 +0330.