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Clinical and Molecular Characteristics of Neuronal Ceroid Lipofuscinosis in Saudi Arabia.
Pediatr Neurol. 2024 Jun;155:149-155. doi: 10.1016/j.pediatrneurol.2024.03.004. Epub 2024 Mar 7.
Pediatr Neurol. 2024.
PMID: 38653183
The First Reported Case of a Child with Two Different Rare Metabolic Disorders: Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13.
Alotaibi M, Alqasmi A, Albassam F, Alkahtani T, Alqahtany M, Alkhaldi M.
Alotaibi M, et al. Among authors: albassam f.
Glob Med Genet. 2023 Oct 10;10(4):278-281. doi: 10.1055/s-0043-1775979. eCollection 2023 Dec.
Glob Med Genet. 2023.
PMID: 37822418
Free PMC article.
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Rituximab in children with myelin oligodendrocyte glycoprotein antibody and relapsing neuroinflammatory disease.
Albassam F, Longoni G, Yea C, Wilbur C, Grover SA, Yeh EA.
Albassam F, et al.
Dev Med Child Neurol. 2020 Mar;62(3):390-395. doi: 10.1111/dmcn.14336. Epub 2019 Aug 30.
Dev Med Child Neurol. 2020.
PMID: 31468511
Free article.
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