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GNE myopathy in the bedouin population of Kuwait: Genetics, prevalence, and clinical description.
Muscle Nerve. 2018 Nov;58(5):700-707. doi: 10.1002/mus.26337. Epub 2018 Oct 3.
Muscle Nerve. 2018.
PMID: 30192030
Whole-exome sequencing identifies mutations in MYMK in a mild form of Carey-Fineman-Ziter syndrome.
Alrohaif H, Töpf A, Evangelista T, Lek M, McArthur D, Lochmüller H.
Alrohaif H, et al.
Neurol Genet. 2018 Mar 19;4(2):e226. doi: 10.1212/NXG.0000000000000226. eCollection 2018 Apr.
Neurol Genet. 2018.
PMID: 29560417
Free PMC article.
No abstract available.
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[When all roads lead to Africa…].
Urtizberea JA, Alrohaif H, Gouda SA, Bastaki L.
Urtizberea JA, et al. Among authors: alrohaif h.
Med Sci (Paris). 2019 Nov;35 Hors série n° 2:15-17. doi: 10.1051/medsci/2019237. Epub 2019 Dec 20.
Med Sci (Paris). 2019.
PMID: 31859625
Free article.
French.
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Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defects.
Roos A, van der Ven PFM, Alrohaif H, Kölbel H, Heil L, Della Marina A, Weis J, Aßent M, Beck-Wödl S, Barresi R, Töpf A, O'Connor K, Sickmann A, Kohlschmidt N, El Gizouli M, Meyer N, Daya N, Grande V, Bois K, Kaiser FJ, Vorgerd M, Schröder C, Schara-Schmidt U, Gangfuss A, Evangelista T, Röbisch L, Hentschel A, Grüneboom A, Fuerst DO, Kuechler A, Tzschach A, Depienne C, Lochmüller H.
Roos A, et al. Among authors: alrohaif h.
Brain. 2023 Oct 3;146(10):4200-4216. doi: 10.1093/brain/awad152.
Brain. 2023.
PMID: 37163662
Free PMC article.
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Case Report: The Genetic Diagnosis of Duchenne Muscular Dystrophy in the Middle East.
Alghamdi F, Al-Tawari A, Alrohaif H, Alshuaibi W, Mansour H, Aartsma-Rus A, Mégarbané A.
Alghamdi F, et al. Among authors: alrohaif h.
Front Pediatr. 2021 Sep 13;9:716424. doi: 10.3389/fped.2021.716424. eCollection 2021.
Front Pediatr. 2021.
PMID: 34595143
Free PMC article.
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