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Items: 18

1.

Farber disease: report of three cases with joint involvement mimicking juvenile idiopathic arthritis.

Moghadam SH, Tavasoli AR, Modaresi M, Ziaee V.

J Musculoskelet Neuronal Interact. 2019 Dec 1;19(4):521-525.

PMID:
31789304
2.

Cinnarizine and sodium valproate as the preventive agents of pediatric migraine: A randomized double-blind placebo-controlled trial.

Amanat M, Togha M, Agah E, Ramezani M, Tavasoli AR, Azizi Malamiri R, Fashandaky F, Heidari M, Salehi M, Eshaghi H, Ashrafi MR.

Cephalalgia. 2019 Nov 10:333102419888485. doi: 10.1177/0333102419888485. [Epub ahead of print]

PMID:
31707814
3.

Persistent dystonia and basal ganglia involvement following metronidazole induced encephalopathy.

Omrani A, Rohani M, Hosseinpour S, Tavasoli AR.

Neurol Sci. 2019 Oct 25. doi: 10.1007/s10072-019-04091-z. [Epub ahead of print] No abstract available.

PMID:
31654363
4.

RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant.

Kameli R, Amanat M, Rezaei Z, Hosseionpour S, Nikbakht S, Alizadeh H, Ashrafi MR, Omrani A, Garshasbi M, Tavasoli AR.

Orphanet J Rare Dis. 2019 Jul 26;14(1):184. doi: 10.1186/s13023-019-1155-9.

5.

Deep brain stimulation in status dystonicus caused by anti-NMDA receptor encephalitis.

Tavasoli AR, Shahidi G, Parvaresh M, Fasano A, Ashrafi MR, Hosseinpour S, Lang AE, Rohani M.

Parkinsonism Relat Disord. 2019 Sep;66:255-257. doi: 10.1016/j.parkreldis.2019.07.023. Epub 2019 Jul 20. No abstract available.

PMID:
31345707
6.

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.

Acta Neurol Belg. 2019 Jun 20. doi: 10.1007/s13760-019-01168-6. [Epub ahead of print] Review.

PMID:
31222513
7.

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.

Cephalalgia. 2019 Oct;39(12):1509-1517. doi: 10.1177/0333102419851814. Epub 2019 Jun 1.

PMID:
31154809
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.

Neuropediatrics. 2019 Apr;50(2):130-134. doi: 10.1055/s-0039-1679911. Epub 2019 Feb 21.

PMID:
30791064
9.

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.

Eur J Med Genet. 2019 Feb 13:103629. doi: 10.1016/j.ejmg.2019.02.002. [Epub ahead of print]

PMID:
30769224
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.

Orphanet J Rare Dis. 2018 Aug 3;13(1):130. doi: 10.1186/s13023-018-0876-5.

11.

Genotype, phenotype and in silico pathogenicity analysis of HEXB mutations: Panel based sequencing for differential diagnosis of gangliosidosis.

Mahdieh N, Mikaeeli S, Tavasoli AR, Rezaei Z, Maleki M, Rabbani B.

Clin Neurol Neurosurg. 2018 Apr;167:43-53. doi: 10.1016/j.clineuro.2018.02.011. Epub 2018 Feb 8.

PMID:
29448188
12.

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.

J Child Neurol. 2018 Mar;33(4):255-259. doi: 10.1177/0883073817751804. Epub 2018 Jan 15.

PMID:
29333903
13.

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

Ashrafi MR, Tavasoli AR, Alizadeh H, Zare Noghabi J, Parvaneh N.

Iran J Child Neurol. 2017 Spring;11(2):69-77.

14.

Neurological and Vascular Manifestations of Ethylmalonic Encephalopathy.

Tavasoli AR, Rostami P, Ashrafi MR, Karimzadeh P.

Iran J Child Neurol. 2017 Spring;11(2):57-60.

15.

Early infantile presentation of 3-methylglutaconic aciduria type 1 with a novel mutation in AUH gene: A case report and literature review.

Tavasoli AR, Shervin Badv R, Zschocke J, Ashrafi MR, Rostami P.

Brain Dev. 2017 Sep;39(8):714-716. doi: 10.1016/j.braindev.2017.04.007. Epub 2017 Apr 21. Review.

PMID:
28438368
16.

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

Ashrafi MR, Tavasoli AR.

Brain Dev. 2017 May;39(5):369-385. doi: 10.1016/j.braindev.2017.01.001. Epub 2017 Jan 20. Review.

PMID:
28117190
17.

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.

Pediatr Neurol. 2014 Oct;51(4):503-8. doi: 10.1016/j.pediatrneurol.2014.05.031. Epub 2014 Jun 6.

PMID:
25023977
18.

Dosimetry of gamma chamber blood irradiator using PAGAT gel dosimeter and Monte Carlo simulations.

Mohammadyari P, Zehtabian M, Sina S, Tavasoli AR, Faghihi R.

J Appl Clin Med Phys. 2014 Jan 4;15(1):3952. doi: 10.1120/jacmp.v15i1.3952.

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