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Page 1
Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized families.
Nat Commun. 2023 Aug 29;14(1):5269. doi: 10.1038/s41467-023-40909-3.
Nat Commun. 2023.
PMID: 37644014
Free PMC article.
Vitamin B12 deficiency secondary to cobalamin F deficiency simulating dyskeratosis congenita.
Altawil L, Alshihry H, Ahmed H, Shamseldin HE, Alkuraya F.
Altawil L, et al. Among authors: alshihry h.
JAAD Case Rep. 2020 Jul 11;6(9):882-885. doi: 10.1016/j.jdcr.2020.07.011. eCollection 2020 Sep.
JAAD Case Rep. 2020.
PMID: 32875039
Free PMC article.
No abstract available.
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Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutation.
Altawil L, Alshihry H, Alfaraidi H, Alhashem A, Alhumidi A, Alkuraya FS.
Altawil L, et al. Among authors: alshihry h.
JAAD Case Rep. 2021 Jun 12;14:55-58. doi: 10.1016/j.jdcr.2021.06.006. eCollection 2021 Aug.
JAAD Case Rep. 2021.
PMID: 34277909
Free PMC article.
No abstract available.
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Lichen Planus of the Eyelids: Case Report of a Rare Presentation of a Common Dermatosis.
AlEid NM, Ilesanmi ON, Alshehri MA, Alhumidi AA, AlShihry H.
AlEid NM, et al. Among authors: alshihry h.
Cureus. 2024 Mar 30;16(3):e57299. doi: 10.7759/cureus.57299. eCollection 2024 Mar.
Cureus. 2024.
PMID: 38690479
Free PMC article.
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Pseudo-Kaposi sarcoma worsening after leg vein harvest for coronary artery bypass grafting.
Alshihry H, Chisti MA, Hamadah I.
Alshihry H, et al.
Ann Saudi Med. 2014 Mar-Apr;34(2):179-81. doi: 10.5144/0256-4947.2014.179.
Ann Saudi Med. 2014.
PMID: 24894790
Free PMC article.
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Integrin α3 mutation junctional epidermolysis bullosa presenting with hypotrichosis and lacrimal obstruction.
Alshihry H, AlGhamdy SD, Alhashem A, Almohanna HM.
Alshihry H, et al.
JAAD Case Rep. 2023 Oct 30;43:76-79. doi: 10.1016/j.jdcr.2023.10.007. eCollection 2024 Jan.
JAAD Case Rep. 2023.
PMID: 38223367
Free PMC article.
No abstract available.
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