Al-Manea W - Search Results

1

The phenotype of a CASQ2 mutation in a Saudi family with catecholaminergic polymorphic ventricular tachycardia.

Al-Hassnan ZN, Tulbah S, Al-Manea W, Al-Fayyadh M. Al-Hassnan ZN, et al. Among authors: al manea w. Pacing Clin Electrophysiol. 2013 May;36(5):e140-2. doi: 10.1111/j.1540-8159.2012.03434.x. Epub 2012 May 31. Pacing Clin Electrophysiol. 2013. PMID: 22650415

2

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: al manea w. 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

3

Appropriate and Inappropriate Implantable Cardioverter Defibrillators Therapies in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia Patients.

Al-Ghamdi B, Mallawi Y, Shafquat A, AlRuwaili N, Alhazaymeh A, Al-Manea W, Al-Fayyadh M. Al-Ghamdi B, et al. Among authors: al manea w. Cardiol Res. 2018 Aug;9(4):204-214. doi: 10.14740/cr734w. Epub 2018 Aug 10. Cardiol Res. 2018. PMID: 30116448 Free PMC article.

4

Phenotypic variability in a series of four pediatric patients with Andersen-Tawil syndrome: A Saudi experience.

Alrashed NA, Al-Manea WM, Tulbah SA, Al-Hassnan ZN. Alrashed NA, et al. Among authors: al manea wm. Int J Pediatr Adolesc Med. 2019 Dec;6(4):158-164. doi: 10.1016/j.ijpam.2019.06.005. Epub 2019 Jun 14. Int J Pediatr Adolesc Med. 2019. PMID: 31890843 Free PMC article.

5

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

6

Clinical and Genetic Characteristics of Arrhythmogenic Right Ventricular Cardiomyopathy Patients: A Single-Center Experience.

Al-Ghamdi BS, Alhadeq F, Alqahtani A, Alruwaili N, Rababh M, Alghamdi S, Almanea W, Alhassnan Z. Al-Ghamdi BS, et al. Cardiol Res. 2023 Oct;14(5):379-386. doi: 10.14740/cr1531. Epub 2023 Oct 21. Cardiol Res. 2023. PMID: 37936624 Free PMC article.

7

Ritscher-Schinzel (cranio-cerebello-cardiac, 3C) syndrome: report of four new cases with renal involvement.

Seidahmed MZ, Alkuraya FS, Shaheed M, Al Zahrani M, Al Manea W, Mansour F, Mustafa T, Farid G, Salih MA. Seidahmed MZ, et al. Among authors: al manea w. Am J Med Genet A. 2011 Jun;155A(6):1393-7. doi: 10.1002/ajmg.a.33966. Epub 2011 May 12. Am J Med Genet A. 2011. PMID: 21567916

8

Severe tortuosity and stenosis of the systemic, pulmonary and coronary vessels in 12 patients with similar phenotypic features: a new syndrome?

Al Fadley F, Al Manea W, Nykanen DG, Al Fadley A, Bulbul Z, Al Halees Z. Al Fadley F, et al. Among authors: al manea w. Cardiol Young. 2000 Nov;10(6):582-9. doi: 10.1017/s1047951100008854. Cardiol Young. 2000. PMID: 11117390

9

Diffuse pulmonary arteriovenous malformation: unusual cause of cyanosis in infancy.

Al-Qurashi M, Ghazal Y, Al Oufi S, Al Manea W. Al-Qurashi M, et al. Among authors: al manea w. Ann Saudi Med. 2000 Mar;20(2):144-6. doi: 10.5144/0256-4947.2000.144. Ann Saudi Med. 2000. PMID: 17322714 Free article. No abstract available.

10

Cardiac rhythm recorded by implanted loop recorder during lightning strike.

Altalhi A, Al-Manea W, Alqweai N, Alothman M. Altalhi A, et al. Among authors: al manea w. Ann Saudi Med. 2017 Sep-Oct;37(5):401-402. doi: 10.5144/0256-4947.2017.401. Ann Saudi Med. 2017. PMID: 28988255 Free PMC article.

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