Muthaffar O - Search Results

1

Patient demographics and characteristics from an ambispective, observational study of patients with duchenne muscular dystrophy in Saudi Arabia.

AlSaman AS, Al Ghamdi F, Bamaga AK, AlShaikh N, Al Muqbil M, Muthaffar O, Bashiri FA, Ali B, Mulayim A, Heider E, Alshahrani AA, Al Muhaizea MA. AlSaman AS, et al. Among authors: muthaffar o. Front Pediatr. 2022 Sep 30;10:1020059. doi: 10.3389/fped.2022.1020059. eCollection 2022. Front Pediatr. 2022. PMID: 36275069 Free PMC article.

2

Reply from the author.

Muthaffar O. Muthaffar O. Saudi Med J. 2014 Nov;35(11):1419. Saudi Med J. 2014. PMID: 25774399 No abstract available.

3

Rasmussen encephalitis: Response to early immunotherapy in a case of immune-mediated encephalitis.

Liba Z, Muthaffar O, Tang J, Minassian B, Halliday W, Branson H, Ann Yeh E. Liba Z, et al. Among authors: muthaffar o. Neurol Neuroimmunol Neuroinflamm. 2015 Feb 12;2(2):e69. doi: 10.1212/NXI.0000000000000069. eCollection 2015 Apr. Neurol Neuroimmunol Neuroinflamm. 2015. PMID: 25738166 Free PMC article. No abstract available.

4

Acute hemiplegia as a rare presentation of infantile Guillain-Barré syndrome.

Muthaffar OY, Mahmoud AA, Al-Saman AS. Muthaffar OY, et al. Saudi Med J. 2014 Aug;35(8):861-4. Saudi Med J. 2014. PMID: 25129187

5

Saudi Epilepsy Society consensus on epilepsy management during the COVID-19 Pandemic.

Alotaibi F, Althani Z, Aljaafari D, Tayeb HO, Baarmah D, Aljalal N, Muthaffar O, Alqulaiti K, Alhameed M, Ali B, Qureshi S, Albaradie R. Alotaibi F, et al. Among authors: muthaffar o. Neurosciences (Riyadh). 2020 Jul;25(3):222-225. doi: 10.17712/nsj.2020.3.20200066. Neurosciences (Riyadh). 2020. PMID: 32683406 Free PMC article. No abstract available.

6

Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly.

Naseer MI, Abdulkareem AA, Muthaffar OY, Sogaty S, Alkhatabi H, Almaghrabi S, Chaudhary AG. Naseer MI, et al. Front Pediatr. 2021 Feb 11;8:627122. doi: 10.3389/fped.2020.627122. eCollection 2020. Front Pediatr. 2021. PMID: 33643967 Free PMC article.

7

Consensus Statement on the Management of Duchenne Muscular Dystrophy in Saudi Arabia During the Coronavirus Disease 2019 Pandemic.

Bamaga AK, Alghamdi F, Alshaikh N, Altwaijri W, Bashiri FA, Hundallah K, Abukhaled M, Muthaffar OY, Al-Mehmadi S, Jamaly TA, Al-Muhaizea MA, Al-Saman A. Bamaga AK, et al. Front Pediatr. 2021 Feb 17;9:629549. doi: 10.3389/fped.2021.629549. eCollection 2021. Front Pediatr. 2021. PMID: 33681102 Free PMC article.

8

Whole-Exome Sequencing Reveals a Missense Variant c.1612C>T (p.Arg538Cys) in the BTD Gene Leading to Neuromyelitis Optica Spectrum Disorder in Saudi Families.

Naseer MI, Pushparaj PN, Abdulkareem AA, Muthaffar OY. Naseer MI, et al. Front Pediatr. 2022 Feb 21;9:829251. doi: 10.3389/fped.2021.829251. eCollection 2021. Front Pediatr. 2022. PMID: 35265569 Free PMC article.

9

Next-Generation Sequencing Reveals Novel Homozygous Missense Variant c.934T > C in POLR1C Gene Causing Leukodystrophy and Hypomyelinating Disease.

Naseer MI, Abdulkareem AA, Pushparaj PN, Saharti S, Muthaffar OY. Naseer MI, et al. Front Pediatr. 2022 May 24;10:862722. doi: 10.3389/fped.2022.862722. eCollection 2022. Front Pediatr. 2022. PMID: 35685919 Free PMC article.

10

Whole-Exome Sequencing Identifies Novel SCN1A and CACNB4 Genes Mutations in the Cohort of Saudi Patients With Epilepsy.

Naseer MI, Abdulkareem AA, Rasool M, Algahtani H, Muthaffar OY, Pushparaj PN. Naseer MI, et al. Front Pediatr. 2022 Jun 22;10:919996. doi: 10.3389/fped.2022.919996. eCollection 2022. Front Pediatr. 2022. PMID: 35813387 Free PMC article.

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