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Identification of novel genomic imbalances in Saudi patients with congenital heart disease.
Mol Cytogenet. 2018 Jan 25;11:9. doi: 10.1186/s13039-018-0356-6. eCollection 2018.
Mol Cytogenet. 2018.
PMID: 29416564
Free PMC article.
A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy.
Al-Hassnan ZN, Shinwari ZM, Wakil SM, Tulbah S, Mohammed S, Rahbeeni Z, Alghamdi M, Rababh M, Colak D, Kaya N, Al-Fayyadh M, Alburaiki J.
Al-Hassnan ZN, et al.
BMC Med Genet. 2016 Jan 14;17:3. doi: 10.1186/s12881-016-0267-5.
BMC Med Genet. 2016.
PMID: 26768247
Free PMC article.
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Identification of a novel KCNQ1 mutation in a large Saudi family with long QT syndrome: clinical consequences and preventive implications.
Shinwari ZM, Al-Hazzani A, Dzimiri N, Tulbah S, Mallawi Y, Al-Fayyadh M, Al-Hassnan ZN.
Shinwari ZM, et al.
Clin Genet. 2013 Apr;83(4):370-4. doi: 10.1111/j.1399-0004.2012.01914.x. Epub 2012 Jul 10.
Clin Genet. 2013.
PMID: 22708720
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Clinical profile and mutation spectrum of long QT syndrome in Saudi Arabia: The impact of consanguinity.
Al-Hassnan ZN, Al-Fayyadh M, Al-Ghamdi B, Shafquat A, Mallawi Y, Al-Hadeq F, Tulbah S, Shinwari ZMA, Almesned A, Alakhfash A, Al Fadly F, Hersi AS, Alhayani A, Al-Hashem A, Arafah D, Dzimiri N, Meyer B, Rababh M, Al-Manea W.
Al-Hassnan ZN, et al. Among authors: shinwari zma.
Heart Rhythm. 2017 Aug;14(8):1191-1199. doi: 10.1016/j.hrthm.2017.04.028. Epub 2017 Apr 22.
Heart Rhythm. 2017.
PMID: 28438721
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The Phenotype and Outcome of Infantile Cardiomyopathy Caused by a Homozygous ELAC2 Mutation.
Shinwari ZMA, Almesned A, Alakhfash A, Al-Rashdan AM, Faqeih E, Al-Humaidi Z, Alomrani A, Alghamdi M, Colak D, Alwadai A, Rababh M, Al-Fayyadh M, Al-Hassnan ZN.
Shinwari ZMA, et al.
Cardiology. 2017;137(3):188-192. doi: 10.1159/000465516. Epub 2017 Apr 26.
Cardiology. 2017.
PMID: 28441660
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Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy.
Al-Hassnan ZN, Almesned A, Tulbah S, Alakhfash A, Alhadeq F, Alruwaili N, Alkorashy M, Alhashem A, Alrashdan A, Faqeih E, Alkhalifi SM, Al Humaidi Z, Sogaty S, Azhari N, Bakhaider AM, Al Asmari A, Awaji A, Albash B, Alhabdan M, Alghamdi MA, Alshuaibi W, Al-Hassnan RZ, Alshenqiti A, Alqahtani A, Shinwari Z, Rbabeh M, Takroni S, Alomrani A, Albert Brotons DC, AlQwaee AM, Almanea W, Alfadley FA, Alfayyadh M, Alwadai A.
Al-Hassnan ZN, et al.
Circ Genom Precis Med. 2020 Oct;13(5):504-514. doi: 10.1161/CIRCGEN.120.002969. Epub 2020 Sep 1.
Circ Genom Precis Med. 2020.
PMID: 32870709
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