Tavasoli AR - Search Results

1

The First Comprehensive Cohort of the Duchenne Muscular Dystrophy in Iranian Population: Mutation Spectrum of 314 Patients and Identifying Two Novel Nonsense Mutations.

Zamani G, Hosseini Bereshneh A, Azizi Malamiri R, Bagheri S, Moradi K, Ashrafi MR, Tavasoli AR, Mohammadi M, Badv RS, Ghahvechi Akbari M, Heidari M. Zamani G, et al. Among authors: tavasoli ar. J Mol Neurosci. 2020 Oct;70(10):1565-1573. doi: 10.1007/s12031-020-01594-9. Epub 2020 May 21. J Mol Neurosci. 2020. PMID: 32436198

2

Effects of miglustat on stabilization of neurological disorder in niemann-pick disease type C: Iranian pediatric case series.

Karimzadeh P, Tonekaboni SH, Ashrafi MR, Shafeghati Y, Rezayi A, Salehpour S, Ghofrani M, Taghdiri MM, Rahmanifar A, Zaman T, Aryani O, Shoar BN, Shiva F, Tavasoli A, Houshmand M. Karimzadeh P, et al. J Child Neurol. 2013 Dec;28(12):1599-606. doi: 10.1177/0883073812464526. Epub 2012 Nov 8. J Child Neurol. 2013. PMID: 23143717

3

Diffuse dermal melanocytosis in two patients with Sandhoff disease and mucopolysaccharidosis VI.

Ashrafi MR, Tavasoli A, Shiva S, Parvaneh N, Tamizifar B. Ashrafi MR, et al. Int J Dermatol. 2014 Jun;53(6):736-8. doi: 10.1111/ijd.12303. Epub 2013 Oct 18. Int J Dermatol. 2014. PMID: 24134161

4

Efficacy and safety of cinnarizine in the prophylaxis of migraine in children: a double-blind placebo-controlled randomized trial.

Ashrafi MR, Salehi S, Malamiri RA, Heidari M, Hosseini SA, Samiei M, Tavasoli AR, Togha M. Ashrafi MR, et al. Among authors: tavasoli ar. Pediatr Neurol. 2014 Oct;51(4):503-8. doi: 10.1016/j.pediatrneurol.2014.05.031. Epub 2014 Jun 6. Pediatr Neurol. 2014. PMID: 25023977 Clinical Trial.

5

Efficacy of pregabalin in childhood refractory partial seizure.

Zamani G, Tavasoli A, Zare-Shahabadi A, Rezaei N, Ahmadvand A. Zamani G, et al. Iran J Pediatr. 2014 Feb;24(1):100-4. Epub 2014 Jan 26. Iran J Pediatr. 2014. PMID: 25793053 Free PMC article.

6

Childhood leukodystrophies: A literature review of updates on new definitions, classification, diagnostic approach and management.

Ashrafi MR, Tavasoli AR. Ashrafi MR, et al. Among authors: tavasoli ar. Brain Dev. 2017 May;39(5):369-385. doi: 10.1016/j.braindev.2017.01.001. Epub 2017 Jan 20. Brain Dev. 2017. PMID: 28117190 Review.

7

Neurological and Vascular Manifestations of Ethylmalonic Encephalopathy.

Tavasoli AR, Rostami P, Ashrafi MR, Karimzadeh P. Tavasoli AR, et al. Iran J Child Neurol. 2017 Spring;11(2):57-60. Iran J Child Neurol. 2017. PMID: 28698729 Free PMC article.

8

Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo Diseases.

Ashrafi MR, Tavasoli AR, Alizadeh H, Zare Noghabi J, Parvaneh N. Ashrafi MR, et al. Among authors: tavasoli ar. Iran J Child Neurol. 2017 Spring;11(2):69-77. Iran J Child Neurol. 2017. PMID: 28698732 Free PMC article.

9

The First Report of Relative Incidence of Inherited White Matter Disorders in an Asian Country Based on an Iranian Bioregistry System.

Ashrafi MR, Rezaei Z, Heidari M, Nikbakht S, Malamiri RA, Mohammadi M, Zamani GR, Badv RS, Rostami P, Movahedinia M, Qorbani M, Amanat M, Tavasoli AR. Ashrafi MR, et al. Among authors: tavasoli ar. J Child Neurol. 2018 Mar;33(4):255-259. doi: 10.1177/0883073817751804. Epub 2018 Jan 15. J Child Neurol. 2018. PMID: 29333903

10

Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations.

Tavasoli AR, Parvaneh N, Ashrafi MR, Rezaei Z, Zschocke J, Rostami P. Tavasoli AR, et al. Orphanet J Rare Dis. 2018 Aug 3;13(1):130. doi: 10.1186/s13023-018-0876-5. Orphanet J Rare Dis. 2018. PMID: 30075786 Free PMC article.

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