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Items: 23

1.

A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18.

Safavi M, Haghi Ashtiani MT, Badv RS, Azari-Yam A, Vasei M.

Arch Iran Med. 2019 Oct 1;22(10):627-628.

2.
3.

A novel case report of spinal muscular atrophy with progressive myoclonic epilepsy from Iran.

Shervin Badv R, Nilipour Y, Rahimi-Dehgolan S, Rashidi-Nezhad A, Ghahvechi Akbari M.

Int Med Case Rep J. 2019 May 30;12:155-159. doi: 10.2147/IMCRJ.S202046. eCollection 2019. Erratum in: Int Med Case Rep J. 2019 Jul 12;12:235.

4.

Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies.

Mohammadzadeh A, Akbaroghli S, Aghaei-Moghadam E, Mahdieh N, Badv RS, Jamali P, Kariminejad R, Chavoshzadeh Z, Ghasemi Firouzabadi S, Mansour Ghanaie R, Nozari A, Banihashemi S, Hadipour F, Hadipour Z, Kariminejad A, Najmabadi H, Shafeghati Y, Behjati F.

Cell J. 2019 Oct;21(3):337-349. doi: 10.22074/ cellj.2019.6053. Epub 2019 Jun 15.

5.

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
6.

Impacts of the international economic sanctions on Iranian patients with epilepsy.

Asadi-Pooya AA, Azizimalamiri R, Badv RS, Yarali B, Asadollahi M, Homayoun M, Sharifi S.

Epilepsy Behav. 2019 Jun;95:166-168. doi: 10.1016/j.yebeh.2019.04.011. Epub 2019 May 4.

PMID:
31063932
7.

Hemi-ESES associated with agenesis of the corpus callosum and normal cognition.

Mohammadi M, Kowkabi S, Asadi-Pooya AA, Malamiri RA, Badv RS.

Epilepsy Behav Case Rep. 2019 Feb 10;11:96-98. doi: 10.1016/j.ebcr.2019.01.005. eCollection 2019.

8.

Impact of hematopoietic stem cell transplant on VEP and ABR values of the patients with malignant infantile osteopetrosis.

Badv RS, Dehghani SS, Behfar M, Ahadi B, Tabasi A, Hamidieh AA.

Eur J Paediatr Neurol. 2018 Jul;22(4):718-724. doi: 10.1016/j.ejpn.2018.04.005. Epub 2018 Apr 18.

PMID:
29730165
9.

Pathogenic significance of SCN1A splicing variants causing Dravet syndrome: Improving diagnosis with targeted sequencing for variants by in silico analysis.

Mahdieh N, Mikaeeli S, Badv RS, Shirazi AG, Maleki M, Rabbani B.

Clin Neurol Neurosurg. 2018 Mar;166:80-90. doi: 10.1016/j.clineuro.2018.01.030. Epub 2018 Jan 31.

PMID:
29408779
10.

Efficacy of low glycemic index treatment in epileptic patients: a systematic review.

Rezaei S, Harsini S, Kavoosi M, Badv RS, Mahmoudi M.

Acta Neurol Belg. 2018 Sep;118(3):339-349. doi: 10.1007/s13760-018-0881-4. Epub 2018 Jan 24. Review.

PMID:
29368115
11.

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
12.

Does Parent Report Gross Motor Function Level of Cerebral Palsy Children Impact on the Quality of Life in these Children?

Pashmdarfard M, Amini M, Badv RS, Ghaffarzade Namazi N, Rassafiani M.

Iran J Child Neurol. 2017 Fall;11(4):52-57.

13.

Short-term and long-term efficacy of classical ketogenic diet and modified Atkins diet in children and adolescents with epilepsy: A systematic review and meta-analysis.

Rezaei S, Abdurahman AA, Saghazadeh A, Badv RS, Mahmoudi M.

Nutr Neurosci. 2019 May;22(5):317-334. doi: 10.1080/1028415X.2017.1387721. Epub 2017 Oct 25.

PMID:
29069983
14.

Association of the Single Nucleotide Polymorphisms of the Genes Encoding IL-2 and IFN-γ With Febrile Seizure.

Shahrokhi A, Zare-Shahabadi A, Naeimi Poor M, Sajedi F, Soltani S, Zoghi S, Shervin Badv R, Ashrafi MR, Rezaei N.

Acta Med Iran. 2017 Jun;55(6):354-359.

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.

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.

Acta Neurol Belg. 2017 Mar;117(1):175-182. doi: 10.1007/s13760-016-0732-0. Epub 2016 Dec 7.

PMID:
27928725
17.

Selection of Suitable Reference Genes for Analysis of Salivary Transcriptome in Non-Syndromic Autistic Male Children.

Panahi Y, Salasar Moghaddam F, Ghasemi Z, Hadi Jafari M, Shervin Badv R, Eskandari MR, Pedram M.

Int J Mol Sci. 2016 Oct 12;17(10). pii: E1711.

18.

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.

Neuromuscul Disord. 2016 Jul;26(7):423-7. doi: 10.1016/j.nmd.2016.05.004. Epub 2016 May 9.

PMID:
27234309
19.

The effects of classic ketogenic diet on serum lipid profile in children with refractory seizures.

Zamani GR, Mohammadi M, Ashrafi MR, Karimi P, Mahmoudi M, Badv RS, Tavassoli AR, Azizi Malamiri R.

Acta Neurol Belg. 2016 Dec;116(4):529-534. Epub 2016 Jan 20.

PMID:
26791878
20.

Single nucleotide polymorphisms of TNF-Α gene in febrile seizures.

Zare-Shahabadi A, Ashrafi MR, Shahrokhi A, Soltani S, Zoghi S, Soleimani F, Vameghi R, Badv RS, Rezaei N.

J Neurol Sci. 2015 Sep 15;356(1-2):153-6. doi: 10.1016/j.jns.2015.06.039. Epub 2015 Jun 23.

PMID:
26119396
21.

General movements as a predictive tool of the neurological outcome in term born infants with hypoxic ischemic encephalopathy.

Soleimani F, Badv RS, Momayezi A, Biglarian A, Marzban A.

Early Hum Dev. 2015 Aug;91(8):479-82. doi: 10.1016/j.earlhumdev.2015.05.007. Epub 2015 Jun 10.

PMID:
26070097
22.
23.

CNS structural anomalies in Iranian children with global developmental delay.

Zamani GR, Shervin-Badv R, Niksirat A, Alizadeh H.

Iran J Child Neurol. 2013 Winter;7(1):25-8.

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