Mohammad Ghofrani
Overview
Explore the profile of Mohammad Ghofrani including associated specialties, affiliations and a list of published articles.
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34
Citations
190
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Recent Articles
11.
Taghdiri M, Omidbeigi M, Asaadi S, Azargashb E, Ghofrani M
Iran J Child Neurol
. 2017 Mar;
11(1):21-28.
PMID: 28277552
Objective: We aimed to find the prognostic factors to detect the patients who fail the treatment of epilepsy, in the early stages of the disease. Materials &methods: This study was...
12.
Alaei M, Talebi S, Ghofrani M, Taghizadeh M, Keramatipour M
Iran Biomed J
. 2016 Jul;
20(5):295-301.
PMID: 27452399
Background: Progressive encephalopathy with or without lipodystrophy is a rare autosomal recessive childhood-onset seipin-associated neurodegenerative syndrome, leading to developmental regression of motor and cognitive skills. In this study, we introduce...
13.
Bakhshandeh Bali M, Rahbarimanesh A, Sadeghi M, Sedighi M, Karimzadeh P, Ghofrani M
Acta Med Iran
. 2015 May;
53(5):276-80.
PMID: 26024701
Migraine involves 5-10% of children and adolescents. Thirty percent of children with severe migraine attacks have school absence and reduced quality of life that need preventive therapy. The purpose of...
14.
Taghdiri M, Bakhshandeh Bali M, Karimzadeh P, Ashrafi M, Tonekaboni S, Ghofrani M
Iran J Child Neurol
. 2015 Mar;
9(1):49-55.
PMID: 25767539
Objective: Approximately one third of epileptic children are resistant to anticonvulsant drugs. This study evaluates the effectiveness, safety, and tolerability of pregabalin as adjunctive therapy in epileptic children relative to...
15.
Karimzadeh P, Jafari N, Nejad Biglari H, Rahimian E, Ahmadabadi F, Nemati H, et al.
Iran J Child Neurol
. 2015 Feb;
8(4):66-71.
PMID: 25657773
Objective: Canavan's disease is a lethal illness caused by a single gene mutation that is inherited as an autosomal recessive pattern. It has many different clinical features especially in the...
16.
Karimzadeh P, Jafari N, Biglari H, Jabbeh Dari S, Ahmad Abadi F, Alaee M, et al.
Iran J Child Neurol
. 2014 Aug;
8(3):55-60.
PMID: 25143775
Objective: GM2-Gangliosidosis disease is a rare autosomal recessive genetic disorder that includes two disorders (Tay-Sachs and Sandhoff disease).These disorders cause a progressive deterioration of nerve cells and inherited deficiency in...
17.
Karimzadeh P, Sedighi M, Beheshti M, Azargashb E, Ghofrani M, Abdollahe-Gorgi F
Seizure
. 2014 May;
23(7):570-2.
PMID: 24795151
Purpose: Intractable epilepsy is a challenging aspects of pediatric epilepsy. This study was conducted to determine the efficacy and tolerability of Low Glycemic Index Treatment (LGIT) in pediatric patients referred...
18.
Karimzadeh P, Jafari N, Ahmad Abadi F, Jabbedari S, Taghdiri M, Alaee M, et al.
Iran J Child Neurol
. 2014 Mar;
8(1):58-61.
PMID: 24665329
Objective: Propionic acidemia is one of the rare congenital neurometabolic disorders with autosomal recessive inheritance. This disorder is caused by a defect in the propionyl-CoA carboxylase enzyme and can be...
19.
Karimzadeh P, Ahmadabadi F, Jafari N, Jabbehdari S, Alaee M, Ghofrani M, et al.
Iran J Child Neurol
. 2014 Mar;
7(4):47-52.
PMID: 24665318
Objective: Biotinidase deficiency is one of the rare congenital metabolic disorders with autosomal recessive inheritance. If this disorder is diagnosed in newborn period, could be prevented well from mental and...
20.
Ghofrani M
Iran J Child Neurol
. 2014 Mar;
7(4):1-5.
PMID: 24665310
The approach to a child who has experienced a first unprovoked generalized tonic-clonic seizure is challenging and at the same time controversial. How to establish the diagnosis, ways and means...