Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

15 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Homozygous premature truncation of the HERG protein : the human HERG knockout.
Hoorntje T, Alders M, van Tintelen P, van der Lip K, Sreeram N, van der Wal A, Mannens M, Wilde A. Hoorntje T, et al. Among authors: van der wal a, van tintelen p, van der lip k. Circulation. 1999 Sep 21;100(12):1264-7. doi: 10.1161/01.cir.100.12.1264. Circulation. 1999. PMID: 10491368
A sodium-channel mutation causes isolated cardiac conduction disease.
Tan HL, Bink-Boelkens MT, Bezzina CR, Viswanathan PC, Beaufort-Krol GC, van Tintelen PJ, van den Berg MP, Wilde AA, Balser JR. Tan HL, et al. Among authors: van tintelen pj, van den berg mp. Nature. 2001 Feb 22;409(6823):1043-7. doi: 10.1038/35059090. Nature. 2001. PMID: 11234013
Longitudinal Prediction of Ventricular Arrhythmic Risk in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy.
Carrick RT, Te Riele ASJM, Gasperetti A, Bosman L, Muller SA, Pendleton C, Tichnell C, Murray B, Yap SC, van den Berg MP, Wilde A, Zeppenfeld K, Hays A, Zimmerman SL, Tandri H, Cadrin-Tourigny J, van Tintelen P, Calkins H, James CA, Wu KC. Carrick RT, et al. Among authors: van tintelen p. Circ Arrhythm Electrophysiol. 2022 Nov;15(11):e011207. doi: 10.1161/CIRCEP.122.011207. Epub 2022 Oct 31. Circ Arrhythm Electrophysiol. 2022. PMID: 36315818 Free PMC article.
TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy.
Alaamery M, Albesher N, Alhabshan F, Barnett P, Salim Kabbani M, Chaikhouni F, Ilgun A, Mook ORF, Alsaif H, Christoffels VM, van Tintelen P, Wilde AAM, Houweling AC, Massadeh S, Postma AV. Alaamery M, et al. Among authors: van tintelen p. J Cardiovasc Dev Dis. 2023 Nov 9;10(11):455. doi: 10.3390/jcdd10110455. J Cardiovasc Dev Dis. 2023. PMID: 37998513 Free PMC article.
Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis.
Corrado D, van Tintelen PJ, McKenna WJ, Hauer RNW, Anastastakis A, Asimaki A, Basso C, Bauce B, Brunckhorst C, Bucciarelli-Ducci C, Duru F, Elliott P, Hamilton RM, Haugaa KH, James CA, Judge D, Link MS, Marchlinski FE, Mazzanti A, Mestroni L, Pantazis A, Pelliccia A, Marra MP, Pilichou K, Platonov PGA, Protonotarios A, Rampazzo A, Saffitz JE, Saguner AM, Schmied C, Sharma S, Tandri H, Te Riele ASJM, Thiene G, Tsatsopoulou A, Zareba W, Zorzi A, Wichter T, Marcus FI, Calkins H; International Experts. Corrado D, et al. Among authors: van tintelen pj. Eur Heart J. 2020 Apr 7;41(14):1414-1429. doi: 10.1093/eurheartj/ehz669. Eur Heart J. 2020. PMID: 31637441 Free PMC article. No abstract available.
Familial occurrence of isolated non-compaction cardiomyopathy.
Lorsheyd A, Cramer MJ, Velthuis BK, Vonken EJ, van der Smagt J, van Tintelen P, Hauer RN. Lorsheyd A, et al. Among authors: van der smagt j, van tintelen p. Eur J Heart Fail. 2006 Dec;8(8):826-31. doi: 10.1016/j.ejheart.2006.02.014. Epub 2006 May 19. Eur J Heart Fail. 2006. PMID: 16713736 Free article.
Periodontal Ehlers-Danlos syndrome is associated with leukoencephalopathy.
Kapferer-Seebacher I, Waisfisz Q, Boesch S, Bronk M, van Tintelen P, Gizewski ER, Groebner R, Zschocke J, van der Knaap MS. Kapferer-Seebacher I, et al. Among authors: van tintelen p. Neurogenetics. 2019 Mar;20(1):1-8. doi: 10.1007/s10048-018-0560-x. Epub 2018 Dec 8. Neurogenetics. 2019. PMID: 30535813 Free PMC article.
15 results