Ashrafi MR - Search Results

1

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.

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

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.

4

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.

5

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

6

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.

7

Leukoencephalopathy in RIN2 syndrome: Novel mutation and expansion of clinical spectrum.

Kameli R, Ashrafi MR, Ehya F, Alizadeh H, Hosseinpour S, Garshasbi M, Tavasoli AR. Kameli R, et al. Among authors: ashrafi mr. Eur J Med Genet. 2020 Jan;63(1):103629. doi: 10.1016/j.ejmg.2019.02.002. Epub 2019 Feb 13. Eur J Med Genet. 2020. PMID: 30769224

8

Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated Patients.

Rezaei Z, Hosseinpour S, Ashrafi MR, Mahdieh N, Alizadeh H, Mohammadpour M, Khosroshahi N, Amanat M, Tavasoli AR. Rezaei Z, et al. Among authors: ashrafi mr. Neuropediatrics. 2019 Apr;50(2):130-134. doi: 10.1055/s-0039-1679911. Epub 2019 Feb 21. Neuropediatrics. 2019. PMID: 30791064

9

Levetiracetam for prophylactic treatment of pediatric migraine: A randomized double-blind placebo-controlled trial.

Montazerlotfelahi H, Amanat M, Tavasoli AR, Agah E, Zamani GR, Sander JW, Badv RS, Mohammadi M, Dehghani M, Heidari M, Hosseini SA, Salehi M, Ashrafi MR. Montazerlotfelahi H, et al. Among authors: ashrafi mr. Cephalalgia. 2019 Oct;39(12):1509-1517. doi: 10.1177/0333102419851814. Epub 2019 Jun 1. Cephalalgia. 2019. PMID: 31154809 Clinical Trial.

10

Primary creatine deficiency syndrome as a potential missed diagnosis in children with psychomotor delay and seizure: case presentation with two novel variants and literature review.

Rostami P, Hosseinpour S, Ashrafi MR, Alizadeh H, Garshasbi M, Tavasoli AR. Rostami P, et al. Among authors: ashrafi mr. Acta Neurol Belg. 2020 Jun;120(3):511-516. doi: 10.1007/s13760-019-01168-6. Epub 2019 Jun 20. Acta Neurol Belg. 2020. PMID: 31222513 Review.

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