Farzad Ahmad Abadi
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Explore the profile of Farzad Ahmad Abadi including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
46
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Recent Articles
1.
Karimzadeh P, Ebrahimi M, Etemad K, Ahmad Abadi F, Hosseini Nezhad Z
Iran J Child Neurol
. 2024 Apr;
18(2):127-140.
PMID: 38617391
Abstract: Gangliosidosis is one of the hereditary metabolic diseases caused by the accumulation of Gangliosid in the central nervous system, leading to severe and progressive neurological deficits. Regarding phenotype, GM1...
2.
Karimzadeh P, Jafari N, Biglari H, Jabbehdari S, Khayat Zadeh S, Ahmad Abadi F, et al.
Iran J Child Neurol
. 2016 Jul;
10(3):73-81.
PMID: 27375759
Objective: We aimed to investigate the clinical and para clinical manifestations of neuro metabolic disorders, in patients who presented by neuro developmental delay in their neuro developmental milestones. Materials &...
3.
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...
4.
Yaghini O, Tonekaboni S, Amir Shahkarami S, Ahmad Abadi F, Shariat F, Abdollah Gorji F
Indian J Pediatr
. 2014 Aug;
82(3):225-9.
PMID: 25106841
Objective: To elucidate the effects of antiepileptic drugs (AEDs) on bone health status of ambulatory epileptic children. Methods: A total of 120 epileptic children aged 2-15 y were enrolled in...
5.
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...
6.
Karimzadeh P, Jafari N, Ahmad Abadi F, Jabbedari S, Taghdiri M, Nemati H, et al.
Iran J Child Neurol
. 2014 Mar;
7(3):63-6.
PMID: 24665309
Objective: Methylmalonic acidemia is one of the inborn errors of metabolism resulting in the accumulation of acylcarnitine in blood and increased urinary methylmalonic acid excretion. This disorder can have symptoms,...