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Year | Number of Results |
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2012 | 1 |
2013 | 2 |
2014 | 1 |
2018 | 1 |
2022 | 1 |
2024 | 0 |
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Page 1
Type III spinal muscular atrophy mimicking muscular dystrophies.
Pediatr Neurol. 2013 May;48(5):363-6. doi: 10.1016/j.pediatrneurol.2012.12.027.
Pediatr Neurol. 2013.
PMID: 23583053
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.
Front Pediatr. 2022 Sep 30;10:1020059. doi: 10.3389/fped.2022.1020059. eCollection 2022.
Front Pediatr. 2022.
PMID: 36275069
Free PMC article.
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FARS2 deficiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance.
Almannai M, Wang J, Dai H, El-Hattab AW, Faqeih EA, Saleh MA, Al Asmari A, Alwadei AH, Aljadhai YI, AlHashem A, Tabarki B, Lines MA, Grange DK, Benini R, Alsaman AS, Mahmoud A, Katsonis P, Lichtarge O, Wong LC.
Almannai M, et al. Among authors: alsaman as.
Mol Genet Metab. 2018 Nov;125(3):281-291. doi: 10.1016/j.ymgme.2018.07.014. Epub 2018 Jul 29.
Mol Genet Metab. 2018.
PMID: 30177229
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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
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Diagnostic uncertainty of tumefactive cystic demyelinating lesions.
Almalki DM, Mudhafar OY, Alsaman AS, Mahmoud AA.
Almalki DM, et al. Among authors: alsaman as.
Neurosciences (Riyadh). 2013 Apr;18(2):176-7.
Neurosciences (Riyadh). 2013.
PMID: 23545620
No abstract available.
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A case of extreme prematurity and delayed diagnosis of pyridoxine-dependent epilepsy.
Al-Saman AS, Rizk TM.
Al-Saman AS, et al.
Neurosciences (Riyadh). 2012 Oct;17(4):371-3.
Neurosciences (Riyadh). 2012.
PMID: 23022904
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