Soroor Inaloo
Overview
Explore the profile of Soroor Inaloo including associated specialties, affiliations and a list of published articles.
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Articles
32
Citations
157
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Recent Articles
1.
Ashrafi M, Babaee M, Hashemi Nazari S, Barzegar M, Ghazavi M, Toosi M, et al.
J Neuromuscul Dis
. 2025 Feb;
11(6):1190-1199.
PMID: 39967428
Background: Three medications have been approved for spinal muscular atrophy (SMA) treatment. No head-to-head clinical trials have directly compared the efficacy of nusinersen and risdiplam. We compare the efficacy of...
2.
Sahebi K, Foroozand H, Bahmei M, Taghizadeh R, Zare S, Inaloo S
Heliyon
. 2025 Feb;
11(2):e41675.
PMID: 39897933
The widespread use of glucocorticoids in clinical practice may occasionally be complicated by hypokalemic paralysis. Previously, only a few cases of glucocorticoid-induced hypokalemic paralysis in healthy adults had been reported....
3.
Nemati H, Modanlou A, Shorafae E, Taghizade R, Inaloo S
Iran J Child Neurol
. 2025 Feb;
19(1):15-23.
PMID: 39896696
Objectives: Epilepsy is one of the most common health problems in Iran. Considering this issue, the present study aimed to investigate New-Onset Refractory Status Epilepticus (NORSE) and Febrile Infection-Related Epilepsy...
4.
Mansouri V, Heidari M, Bemanalizadeh M, Azizimalamiri R, Nafissi S, Ghahvechi Akbari M, et al.
J Neuromuscul Dis
. 2023 Feb;
10(2):211-225.
PMID: 36776076
Background: Insufficient amounts of survival motor neuron protein is leading to one of the most disabling neuromuscular diseases, spinal muscular atrophy (SMA). Before the current study, the detailed characteristics of...
5.
Moravej H, Inaloo S, Nahid S, Mazloumi S, Nemati H, Moosavian T, et al.
Indian Pediatr
. 2023 Jan;
60(3):193-196.
PMID: 36604934
Objective: This study aimed to find the common inborn errors of metabolism in Iranian patients with autism spectrum disorder. Methods: In this cross-sectional multicenter study, 105 children and adolescents with...
6.
Abdollahifard S, Kheshti F, Inaloo S
Iran J Child Neurol
. 2022 Oct;
16(3):213-217.
PMID: 36204446
Case Presentation: The first case was a 4-year-old female patient who firstly presented with nausea and vomiting; then, the case was discharged; however, 1 week later, the case was returned...
7.
Nemati H, Boroujeni A, Inaloo S, Katibeh P, Shahriari M
Neurol India
. 2021 Nov;
69(5):1343-1348.
PMID: 34747809
Background And Objectives: Folate is an important vitamin with a significant role in cell metabolism processes, and its deficiency is associated with several diseases. In addition, cerebral folate deficiency is...
8.
Nejabat M, Inaloo S, Taghipour Sheshdeh A, Bahramjahan S, Sarvestani F, Katibeh P, et al.
Front Pediatr
. 2021 Sep;
9:734946.
PMID: 34540776
Cerebral palsy (CP) is a heterogeneous permanent disorder impacting movement and posture. Investigations aimed at diagnosing this disorder are expensive and time-consuming and can eventually inconclusive. This study aimed to...
9.
Paktinat M, Hessami K, Inaloo S, Nemati H, Katibeh P, Nejabat M, et al.
Int J Pediatr
. 2021 Mar;
2021:6695119.
PMID: 33777149
Introduction: Acute necrotizing encephalopathy (ANE), a rare entity with unique clinical presentation, can be associated significant morbidity and mortality. The majority of ANE reported cases are sporadic. However, reports of...
10.
Habibzadeh P, Tabatabaei Z, Inaloo S, Nashatizadeh M, Synofzik M, Ostovan V, et al.
Front Genet
. 2021 Jan;
11:585136.
PMID: 33414805
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a rare neurodegenerative disorder caused by biallelic mutations in the gene. Once thought to be limited to Charlevoix-Saguenay region of Quebec, recent...