Výsledky vyhledávání - "Mira Almheiri"

Akademický článek

Six-year follow-up of a child with familial chylomicronemia syndrome: disease course and effectiveness of gemfibrozil treatment --case report and literature review

Autor: Manal Mustafa, Mira Almheiri

Publikováno v: Annals of Pediatric Endocrinology & Metabolism, Vol 29, Iss 2, Pp 130-134 (2024)

Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disease affecting lipoprotein metabolism. FCS is estimated to occur in 1 in 1–2 million individuals and can be diagnosed at any age, equally affecting all genders, races, and eth

Externí odkaz: https://doaj.org/article/637a5610c1c64ae28dc5c44fe6af0225

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Periodical

Data on Familial Chylomicronemia Syndrome Reported by Mira Almheiri and Colleagues (Six-year follow-up of a child with familial chylomicronemia syndrome: disease course and effectiveness of gemfibrozil treatment -- Case report and literature...).

Publikováno v: Pediatrics Week; 2/2/2024, p86-86, 1p

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Akademický článek

Six-year follow-up of a child with familial chylomicronemia syndrome: disease course and effectiveness of gemfibrozil treatment --case report and literature review.

Autor: Mustafa, Manal¹ flowers.garden2222@gmail.com, Almheiri, Mira¹

Publikováno v: Annals of Pediatric Endocrinology & Metabolism. Apr2024, Vol. 29 Issue 2, p130-134. 5p.

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Akademický článek

ESPGHAN 56th Annual Meeting Abstracts.

Publikováno v: JPGN Reports; May2024 Supplement 1, Vol. 5, pS1-S1437, 1437p

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Akademický článek

Abstracts of the ESPE 61 Annual Society Meeting.

Publikováno v: Hormone Research in Paediatrics; 2023 Suppl 4, Vol. 96, p1-643, 643p

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Akademický článek

ESPGHAN 55th Annual Meeting Abstracts.

Publikováno v: Journal of Pediatric Gastroenterology & Nutrition; Jun2023Supplement, Vol. 76, p1-1407, 1407p

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