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The following term was not found in PubMed: Daiyoub
Page 1
Modern approaches to the management of homozygous familial hypercholesterolemia in the Middle East and North Africa.
J Clin Lipidol. 2024 Mar-Apr;18(2):e132-e141. doi: 10.1016/j.jacl.2023.12.003. Epub 2023 Dec 15.
J Clin Lipidol. 2024.
PMID: 38158247
Free article.
Review.
Physio-molecular responses of tomato cultivars to biotic stress: Exploring the interplay between Alternaria alternata OP881811 infection and plant defence mechanisms.
Adss IA, Al-Huqail AA, Khan F, El-Shamy SS, Amer GM, Hafez EE, Ibrahim OM, Sobhy SE, Saleh AA.
Adss IA, et al.
Plant Physiol Biochem. 2024 Feb;207:108421. doi: 10.1016/j.plaphy.2024.108421. Epub 2024 Feb 3.
Plant Physiol Biochem. 2024.
PMID: 38335887
Subsequently, fourteen diverse tomato cultivars; Cv Ferment, Cv 103, Cv Damber, Cv 186, Cv 4094, Cv Angham, Cv N 17, Cv Gesma, Cv 010, Cv branch, cv 2020, Cv 023, Cv Gana and Cv 380 were meticulously assessed to discern their susceptibility levels upon inoculation with Alt …
Subsequently, fourteen diverse tomato cultivars; Cv Ferment, Cv 103, Cv Damber, Cv 186, Cv 4094, Cv Angham, Cv N 17, Cv Gesma, Cv 010 …
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Whole exome sequencing reveals a homozygous nonsense mutation in HEXA gene leading to Tay-Sachs disease in Saudi Family.
Naseer MI, Abdulkareem AA, Jan MM, Chaudhary AG, Al-Qahtani MH.
Naseer MI, et al.
Pak J Med Sci. 2020 Sep-Oct;36(6):1425-1428. doi: 10.12669/pjms.36.6.2579.
Pak J Med Sci. 2020.
PMID: 32968423
Free PMC article.
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Mutation of the CYP2R1 vitamin D 25-hydroxylase in a Saudi Arabian family with severe vitamin D deficiency.
Al Mutair AN, Nasrat GH, Russell DW.
Al Mutair AN, et al.
J Clin Endocrinol Metab. 2012 Oct;97(10):E2022-5. doi: 10.1210/jc.2012-1340. Epub 2012 Aug 1.
J Clin Endocrinol Metab. 2012.
PMID: 22855339
Free PMC article.
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Genetic and diabetic auto-antibody markers in Saudi children with type 1 diabetes.
Manan H, Angham AM, Sitelbanat A.
Manan H, et al.
Hum Immunol. 2010 Dec;71(12):1238-42. doi: 10.1016/j.humimm.2010.09.008. Epub 2010 Sep 19.
Hum Immunol. 2010.
PMID: 20858521
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Novel compound heterozygous mutations in WDR62 gene leading to developmental delay and Primary Microcephaly in Saudi Family.
Naseer MI, Rasool M, Abdulkareem AA, Chaudhary AG, Zaidi SK, Al-Qahtani MH.
Naseer MI, et al.
Pak J Med Sci. 2019;35(3):764-770. doi: 10.12669/pjms.35.3.36.
Pak J Med Sci. 2019.
PMID: 31258591
Free PMC article.
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