Bhuiyan ZA - Search Results

1

Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience.

Bhuiyan ZA, Klein M, Hammond P, van Haeringen A, Mannens MM, Van Berckelaer-Onnes I, Hennekam RC. Bhuiyan ZA, et al. J Med Genet. 2006 Jul;43(7):568-75. doi: 10.1136/jmg.2005.038240. Epub 2005 Oct 19. J Med Genet. 2006. PMID: 16236812 Free PMC article.

2

Simultaneous analysis of the behavioural phenotype, physical factors, and parenting stress in people with Cornelia de Lange syndrome.

Wulffaert J, van Berckelaer-Onnes I, Kroonenberg P, Scholte E, Bhuiyan Z, Hennekam R. Wulffaert J, et al. J Intellect Disabil Res. 2009 Jul;53(7):604-19. doi: 10.1111/j.1365-2788.2009.01185.x. J Intellect Disabil Res. 2009. PMID: 19522789

3

A Malay boy with the Cornelia de Lange syndrome: clinical and molecular findings.

Bhuiyan ZA, Zilfalil BA, Hennekam RC. Bhuiyan ZA, et al. Singapore Med J. 2006 Aug;47(8):724-7. Singapore Med J. 2006. PMID: 16865217 Free article.

4

Genotype-phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia.

Al-Aama JY, Al-Ghamdi S, Bdier AY, AlQarawi A, Jiman OA, Al-Aama N, Al-Aata J, Wilde AA, Bhuiyan ZA. Al-Aama JY, et al. Among authors: bhuiyan za. Clin Genet. 2015;87(1):74-9. doi: 10.1111/cge.12330. Epub 2013 Dec 27. Clin Genet. 2015. PMID: 24372464

5

Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study.

Cox MG, van der Zwaag PA, van der Werf C, van der Smagt JJ, Noorman M, Bhuiyan ZA, Wiesfeld AC, Volders PG, van Langen IM, Atsma DE, Dooijes D, van den Wijngaard A, Houweling AC, Jongbloed JD, Jordaens L, Cramer MJ, Doevendans PA, de Bakker JM, Wilde AA, van Tintelen JP, Hauer RN. Cox MG, et al. Among authors: bhuiyan za. Circulation. 2011 Jun 14;123(23):2690-700. doi: 10.1161/CIRCULATIONAHA.110.988287. Epub 2011 May 23. Circulation. 2011. PMID: 21606396

6

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families.

Smits JP, Koopmann TT, Wilders R, Veldkamp MW, Opthof T, Bhuiyan ZA, Mannens MM, Balser JR, Tan HL, Bezzina CR, Wilde AA. Smits JP, et al. Among authors: bhuiyan za. J Mol Cell Cardiol. 2005 Jun;38(6):969-81. doi: 10.1016/j.yjmcc.2005.02.024. Epub 2005 Apr 1. J Mol Cell Cardiol. 2005. PMID: 15910881

7

Novel Brugada syndrome-causing mutation in ion-conducting pore of cardiac Na+ channel does not affect ion selectivity properties.

Amin AS, Verkerk AO, Bhuiyan ZA, Wilde AA, Tan HL. Amin AS, et al. Among authors: bhuiyan za. Acta Physiol Scand. 2005 Dec;185(4):291-301. doi: 10.1111/j.1365-201X.2005.01496.x. Acta Physiol Scand. 2005. PMID: 16266370

8

Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome.

Smits JP, Veldkamp MW, Bezzina CR, Bhuiyan ZA, Wedekind H, Schulze-Bahr E, Wilde AA. Smits JP, et al. Among authors: bhuiyan za. Cardiovasc Res. 2005 Aug 15;67(3):459-66. doi: 10.1016/j.cardiores.2005.01.017. Cardiovasc Res. 2005. PMID: 16039271

9

Clinical and genetic analysis of long QT syndrome in two Malay children.

Wong AR, Zilfalil BA, Bhuiyan ZA. Wong AR, et al. Among authors: bhuiyan za. Med J Malaysia. 2019 Aug;74(4):341-343. Med J Malaysia. 2019. PMID: 31424047 Free article.

10

De novo mutation in the SCN5A gene associated with early onset of sudden infant death.

Wedekind H, Smits JP, Schulze-Bahr E, Arnold R, Veldkamp MW, Bajanowski T, Borggrefe M, Brinkmann B, Warnecke I, Funke H, Bhuiyan ZA, Wilde AA, Breithardt G, Haverkamp W. Wedekind H, et al. Among authors: bhuiyan za. Circulation. 2001 Sep 4;104(10):1158-64. doi: 10.1161/hc3501.095361. Circulation. 2001. PMID: 11535573

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