Mir A - Search Results

1

SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population.

Mir A, Almudhry M, Alghamdi F, Albaradie R, Ibrahim M, Aldurayhim F, Alhedaithy A, Alamr M, Bawazir M, Mohammad S, Abdelhay S, Bashir S, Housawi Y. Mir A, et al. Hum Genet. 2022 Jan;141(1):81-99. doi: 10.1007/s00439-021-02404-x. Epub 2021 Nov 19. Hum Genet. 2022. PMID: 34797406

2

Use of Cyclophosphamide in a Child With Fulminant Acute Disseminated Encephalomyelitis.

Ayed H, Chaudhary MW, AlBaradie R, Mir A. Ayed H, et al. Among authors: mir a. Child Neurol Open. 2018 Mar 11;5:2329048X18754631. doi: 10.1177/2329048X18754631. eCollection 2018. Child Neurol Open. 2018. PMID: 29560383 Free PMC article.

3

Biotin-Thiamine-Responsive Basal Ganglia Disease-A Treatable Metabolic Disorder.

Mir A, Alhazmi R, Albaradie R. Mir A, et al. Pediatr Neurol. 2018 Oct;87:80-81. doi: 10.1016/j.pediatrneurol.2018.06.006. Epub 2018 Jul 12. Pediatr Neurol. 2018. PMID: 30119991 No abstract available.

4

Cardioembolic Stroke from an Atrial Myxoma in a Pediatric Patient: A Case Report and Review of the Literature.

Aldajani AA, Mudhry MA, Mir A, Albaradie RS. Aldajani AA, et al. Among authors: mir a. J Heart Valve Dis. 2017 Nov;26(6):646-650. J Heart Valve Dis. 2017. PMID: 30207114 Review.

5

Epilepsy in patients with EAST syndrome caused by mutation in the KCNJ10.

Mir A, Chaudhary M, Alkhaldi H, Alhazmi R, Albaradie R, Housawi Y. Mir A, et al. Brain Dev. 2019 Sep;41(8):706-715. doi: 10.1016/j.braindev.2019.03.009. Epub 2019 Apr 2. Brain Dev. 2019. PMID: 30952461 Review.

6

Corrigendum to "Epilepsy in patients with EAST syndrome caused by mutation in the KCNJ10" [Brain Dev 2019].

Mir A, Chaudhary M, Alkhaldi H, Alhazmi R, Albaradie R, Housawi Y. Mir A, et al. Brain Dev. 2019 Sep;41(8):716. doi: 10.1016/j.braindev.2019.06.007. Epub 2019 Jul 19. Brain Dev. 2019. PMID: 31331637 No abstract available.

7

LGI-1 antibody encephalitis in a seven-year-old girl.

Mir A, Thani Z, Bashir S, Ayed H, Albaradie R. Mir A, et al. Epileptic Disord. 2019 Dec 1;21(6):591-597. doi: 10.1684/epd.2019.1117. Epileptic Disord. 2019. PMID: 31871009

8

Complete resolution of epileptic spasms with vigabatrin in a patient with 3-methylglutaconic aciduria caused by TIMM50 gene mutation.

Mir A, Hadab S, Sammak M, Alhazmi R, Housawi Y, Bashir S. Mir A, et al. Clin Genet. 2020 Jul;98(1):102-103. doi: 10.1111/cge.13763. Epub 2020 May 5. Clin Genet. 2020. PMID: 32369862 No abstract available.

9

GRIN2A -Related Severe Epileptic Encephalopathy Treated with Memantine: An Example of Precision Medicine.

Mir A, Qahtani M, Bashir S. Mir A, et al. J Pediatr Genet. 2020 Dec;9(4):252-257. doi: 10.1055/s-0039-3401028. Epub 2019 Dec 24. J Pediatr Genet. 2020. PMID: 32765929 Free PMC article.

10

Utility of single-photon emission computed tomography (SPECT) in presurgical evaluation of children: A single-center experience.

Mir A, Baradie RA, Alnaim A, Moinuddin A, Khan MI, Jallul T, Otaibi FA, Joseph M, Dossary SA, Bashir S. Mir A, et al. Epilepsy Res. 2020 Nov;167:106445. doi: 10.1016/j.eplepsyres.2020.106445. Epub 2020 Aug 19. Epilepsy Res. 2020. PMID: 33091836

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