Inaloo S - Search Results

1

TSC1 Mutations in Keratoconus Patients With or Without Tuberous Sclerosis.

Bykhovskaya Y, Fardaei M, Khaled ML, Nejabat M, Salouti R, Dastsooz H, Liu Y, Inaloo S, Rabinowitz YS. Bykhovskaya Y, et al. Among authors: inaloo s. Invest Ophthalmol Vis Sci. 2017 Dec 1;58(14):6462-6469. doi: 10.1167/iovs.17-22819. Invest Ophthalmol Vis Sci. 2017. PMID: 29261847 Free PMC article.

2

Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene.

Karimzadeh P, Naderi S, Modarresi F, Dastsooz H, Nemati H, Farokhashtiani T, Shamsian BS, Inaloo S, Faghihi MA. Karimzadeh P, et al. Among authors: inaloo s. BMC Med Genet. 2017 Jul 17;18(1):73. doi: 10.1186/s12881-017-0417-4. BMC Med Genet. 2017. PMID: 28716012 Free PMC article.

3

A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment.

Habibzadeh P, Inaloo S, Silawi M, Dastsooz H, Farazi Fard MA, Sadeghipour F, Faghihi Z, Rezaeian M, Yavarian M, Böhm J, Faghihi MA. Habibzadeh P, et al. Among authors: inaloo s. Front Neurol. 2019 Sep 4;10:944. doi: 10.3389/fneur.2019.00944. eCollection 2019. Front Neurol. 2019. PMID: 31551910 Free PMC article.

4

Multiple sclerosis in children.

Inaloo S, Haghbin S. Inaloo S, et al. Iran J Child Neurol. 2013 Spring;7(2):1-10. Iran J Child Neurol. 2013. PMID: 24665290 Free PMC article. Review.

5

Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

Habibzadeh P, Tabatabaei Z, Inaloo S, Nashatizadeh MM, Synofzik M, Ostovan VR, Faghihi MA. Habibzadeh P, et al. Among authors: inaloo s. Front Genet. 2020 Dec 22;11:585136. doi: 10.3389/fgene.2020.585136. eCollection 2020. Front Genet. 2020. PMID: 33414805 Free PMC article.

6

Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran.

Nejabat M, Inaloo S, Sheshdeh AT, Bahramjahan S, Sarvestani FM, Katibeh P, Nemati H, Tabei SMB, Faghihi MA. Nejabat M, et al. Among authors: inaloo s. Front Pediatr. 2021 Sep 3;9:734946. doi: 10.3389/fped.2021.734946. eCollection 2021. Front Pediatr. 2021. PMID: 34540776 Free PMC article.

7

Case Report of RANBP2 Mutation and Familial Acute Necrotizing Encephalopathy.

Paktinat M, Hessami K, Inaloo S, Nemati H, Katibeh P, Nejabat M, Darabi MH, Bereshneh AH. Paktinat M, et al. Among authors: inaloo s. Int J Pediatr. 2021 Mar 13;2021:6695119. doi: 10.1155/2021/6695119. eCollection 2021. Int J Pediatr. 2021. PMID: 33777149 Free PMC article.

8

The Cerebrospinal Fluid Concentration of Methyltetrahydrofolate and Serum Folate in Children with Developmental Delay, Regression, and/or Refractory Epilepsy.

Nemati H, Boroujeni AF, Inaloo S, Katibeh P, Shahriari M. Nemati H, et al. Among authors: inaloo s. Neurol India. 2021 Sep-Oct;69(5):1343-1348. doi: 10.4103/0028-3886.329526. Neurol India. 2021. PMID: 34747809 Free article.

9

Evaluation of The Metabolic Syndrome Criteria And Body Composition in Ambulatory Children with Epilepsy UsingSodium Valproate and Carbamazepine In Southern Iran: A Case-Control Study.

Inaloo S, Saki F, Paktinat M, Katibeh P, Nemati H, Ranjbar Omrani G. Inaloo S, et al. Iran J Child Neurol. 2020 Summer;14(3):47-56. Iran J Child Neurol. 2020. PMID: 32952581 Free PMC article.

10

Bone mineral density loss in ambulatory children with epilepsy in spite of using supplemental vitamin D in Southern Iran: a case-control study.

Inaloo S, Paktinat M, Saki F, Katibeh P, Nemati H, Dabbaghmanesh MH, Omrani GHR. Inaloo S, et al. J Bone Miner Metab. 2019 May;37(3):537-544. doi: 10.1007/s00774-018-0951-y. Epub 2018 Sep 6. J Bone Miner Metab. 2019. PMID: 30191457

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