Ashrafi MR - Search Results

1

Primary and Secondary Microcephaly, Global Developmental Delay, and Seizure in Two Siblings Caused by a Novel Missense Variant in the ZNF335 Gene.

Tavasoli AR, Memar EHE, Ashrafi MR, Hosseini SMM, Haghighi R, Ghabeli H, Pourbakhtyaran E, Rasoulinezhad M, Mohammadi P, Heidari M. Tavasoli AR, et al. Among authors: ashrafi mr. J Mol Neurosci. 2022 Apr;72(4):719-729. doi: 10.1007/s12031-021-01955-y. Epub 2022 Jan 4. J Mol Neurosci. 2022. PMID: 34982360

2

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. 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.

3

Diagnosis of an abnormality in brain MRI.

Hosseini SA, Ashrafi MR, Heidari M. Hosseini SA, et al. Among authors: ashrafi mr. Iran J Pediatr. 2014 Dec;24(6):779-80. Epub 2014 Aug 12. Iran J Pediatr. 2014. PMID: 26019787 Free PMC article. No abstract available.

4

The quality of life in boys with Duchenne muscular dystrophy.

Zamani G, Heidari M, Azizi Malamiri R, Ashrafi MR, Mohammadi M, Shervin Badv R, Hosseini SA, Salehi S, Shahrokhi A, Qorbani M, Fathi MR. Zamani G, et al. Among authors: ashrafi mr. Neuromuscul Disord. 2016 Jul;26(7):423-7. doi: 10.1016/j.nmd.2016.05.004. Epub 2016 May 9. Neuromuscul Disord. 2016. PMID: 27234309

5

The efficacy of the ketogenic diet in infants and young children with refractory epilepsies using a formula-based powder.

Ashrafi MR, Hosseini SA, Zamani GR, Mohammadi M, Tavassoli A, Badv RS, Heidari M, Karimi P, Malamiri RA. Ashrafi MR, et al. Acta Neurol Belg. 2017 Mar;117(1):175-182. doi: 10.1007/s13760-016-0732-0. Epub 2016 Dec 7. Acta Neurol Belg. 2017. PMID: 27928725 Clinical Trial.

6

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

Ashrafi MR, Tavasoli AR. Ashrafi MR, et al. 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. Among authors: ashrafi mr. 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. 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. 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. Among authors: ashrafi mr. 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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