Habibe Nejad Biglari
Overview
Explore the profile of Habibe Nejad Biglari including associated specialties, affiliations and a list of published articles.
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11
Citations
23
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Recent Articles
1.
Nejad Biglari H, Molaei-Arsangi M, Ahmadipour H, Eftekhar Vaghefi R, Shafieei M, Parvaresh S
Iran J Child Neurol
. 2023 Aug;
17(3):43-54.
PMID: 37637791
Objectives: This study aimed to evaluate patients with focal seizures, their clinical manifestations, and their response to treatment, then compared the accuracy of electroencephalography and Magnetic Resonance Imaging (MRI) to...
2.
Hojabri M, Gilani A, Irilouzadian R, Nejad Biglari H, Sarmadian R
Clin Med Insights Case Rep
. 2023 Jul;
16:11795476231188061.
PMID: 37476682
Background: Primary deficiency of coenzyme Q deficiency-4 (CoQD4) is a heterogeneous disorder affecting different age groups. The main clinical manifestation consists of cerebellar ataxia, exercise intolerance, and dystonia. Case Report:...
3.
Ghoshouni H, Sarmadian R, Irilouzadian R, Nejad Biglari H, Gilani A
J Investig Med High Impact Case Rep
. 2023 Apr;
11:23247096231168109.
PMID: 37083278
Cerebrotendinous xanthomatosis () is a rare hereditary disease described by a mutation in the , which encodes the sterol 27-hydroxylase enzyme involved in the synthesis of bile acid. Accumulation of...
4.
Sarmadian R, Gilani A, Nejad Biglari H
Oxf Med Case Reports
. 2023 Mar;
2023(3):omad024.
PMID: 36993824
Paganini-Miozzo syndrome (MRXSPM) is a rare neurogenetic disorder that is transmitted by X-linked recessive inheritance. This is the third case reported of this disease in the world with a novel...
5.
Irilouzadian R, Goudarzi A, Hesami H, Sarmadian R, Nejad Biglari H, Gilani A
SAGE Open Med Case Rep
. 2023 Mar;
11:2050313X231160885.
PMID: 36968992
Canavan disease is a rare fetal inherited leukodystrophy, caused by accumulation of N-acetyl-aspartate in the brain. Here, we report a child presented with frequent intractable seizures and visual impairment. A...
6.
Karimi H, Sarmadian R, Gilani A, Salajegheh P, Nejad Biglari H, Gholizadeh M
J Med Case Rep
. 2022 Dec;
16(1):452.
PMID: 36471442
Background: Coronavirus disease 2019 can lead to rare but severe and life-threatening diseases in susceptible high-risk populations, including patients with immunodeficiency. A rare event in this report is stroke following...
7.
Tonekaboni S, Mahmoudi S, Abdollah Gorji F, Nejad Biglari H, Taghdiri M, Etemadi K, et al.
Iran J Child Neurol
. 2021 Nov;
15(4):27-34.
PMID: 34782839
Objective: Guillain-Barré Syndrome (GBS) is an acute inflammatory polyneuropathy characterized by a rapid progressive symmetric weakness. The GBS is the most common cause of acute flaccid paralysis (AFP) in most...
8.
Karimzadeh P, Jafari N, Nejad Biglari H, Jabbehdari S, Alizadeh M, Alizadeh G, et al.
Iran J Child Neurol
. 2016 Apr;
10(1):61-4.
PMID: 27057190
Objective: Adrenoleukodystrophy disorder is one of the x-linked genetic disorders caused by the myelin sheath breakdown in the brain. In this study, we present 4 yr experience on this disorder....
9.
Jabbehdari S, Rahimian E, Jafari N, Sanii S, Khayatzadehkakhki S, Nejad Biglari H
Iran J Child Neurol
. 2015 Sep;
9(3):57-61.
PMID: 26401154
Objective: Metachromatic leukodystrophy disorder (MLD) is one of the rare neurometabolic diseases caused due to lack of saposin B and arylsulfatase A enzyme deficiency. Materials & Methods: Eighteen patients diagnosed...
10.
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...