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COVID-19 in Unvaccinated patients with inherited metabolic disorders: A single center experience.
Eur J Med Genet. 2022 Nov;65(11):104602. doi: 10.1016/j.ejmg.2022.104602. Epub 2022 Aug 30.
Eur J Med Genet. 2022.
PMID: 36049607
Free PMC article.
Optic neuropathy in classical methylmalonic acidemia.
AlOwain M, Khalifa OA, Al Sahlawi Z, Hussein MH, Sulaiman RA, Al-Sayed M, Rahbeeni Z, Al-Hassnan Z, Al-Zaidan H, Nezzar H, Al Homoud I, Eldali A, Altonen B, Handoom BS, Mbekeani JN.
AlOwain M, et al. Among authors: handoom bs.
Ophthalmic Genet. 2019 Aug;40(4):313-322. doi: 10.1080/13816810.2019.1634740. Epub 2019 Jul 4.
Ophthalmic Genet. 2019.
PMID: 31269850
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The effects of low protein products availability on growth parameters and metabolic control in selected amino acid metabolism disorders patients.
Handoom B, Megdad E, Al-Qasabi D, Al Mesned M, Hawary R, Al-Nufiee S, Al-Hassnan Z, Alsayed MD, Eldali A.
Handoom B, et al.
Int J Pediatr Adolesc Med. 2018 Jun;5(2):60-68. doi: 10.1016/j.ijpam.2018.04.001. Epub 2018 Jun 14.
Int J Pediatr Adolesc Med. 2018.
PMID: 30805535
Free PMC article.
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Undiagnosed Phenylketonuria Can Exist Everywhere: Results From an International Survey.
van Wegberg AMJ, Trefz F, Gizewska M, Ahmed S, Chabraoui L, Zaki MS, Maillot F, van Spronsen FJ; Study Group on Missed PKU and Missed to Follow-Up.
van Wegberg AMJ, et al.
J Pediatr. 2021 Dec;239:231-234.e2. doi: 10.1016/j.jpeds.2021.08.070. Epub 2021 Aug 30.
J Pediatr. 2021.
PMID: 34474089
Free article.
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