120 related articles for article (PubMed ID: 16360094)
1. Entwining electrical and hypertrophic cardiomyopathies.
Alexander M
Heart Rhythm; 2005 Dec; 2(12):1369-70. PubMed ID: 16360094
[No Abstract] [Full Text] [Related]
2. Syndactyly and long QT syndrome (CaV1.2 missense mutation G406R) is associated with hypertrophic cardiomyopathy.
Lo-A-Njoe SM; Wilde AA; van Erven L; Blom NA
Heart Rhythm; 2005 Dec; 2(12):1365-8. PubMed ID: 16360093
[No Abstract] [Full Text] [Related]
3. The role of genetic testing in paediatric syndromes of sudden death: state of the art and future considerations.
McCormack J
Cardiol Young; 2009 Nov; 19 Suppl 2():54-65. PubMed ID: 19857351
[No Abstract] [Full Text] [Related]
4. Long QT syndrome manifested as fetal ventricular tachycardia and intermittent AV block.
Lin MT; Wu MH; Hsieh FJ; Wang JK; Teng RJ; Tsou KI; Lue HC
Am J Perinatol; 1998 Mar; 15(3):145-7. PubMed ID: 9572367
[TBL] [Abstract][Full Text] [Related]
5. [Genetic aspects of the etiology of arrhythmia].
Thierfelder L
Z Kardiol; 2000; 89 Suppl 3():1-5. PubMed ID: 10810779
[TBL] [Abstract][Full Text] [Related]
6. A rare association of long QT syndrome and syndactyly: Timothy syndrome (LQT 8).
Krause U; Gravenhorst V; Kriebel T; Ruschewski W; Paul T
Clin Res Cardiol; 2011 Dec; 100(12):1123-7. PubMed ID: 21915623
[No Abstract] [Full Text] [Related]
7. Is there a relation between SIDS and long QT syndrome?
Skinner JR
Arch Dis Child; 2005 May; 90(5):445-9. PubMed ID: 15851422
[No Abstract] [Full Text] [Related]
8. Sudden cardiac death in young competitive athletes due to genetic cardiac abnormalities.
Wever-Pinzon OE; Myerson M; Sherrid MV
Anadolu Kardiyol Derg; 2009 Dec; 9 Suppl 2():17-23. PubMed ID: 20089483
[TBL] [Abstract][Full Text] [Related]
9. Unusual causes of sudden cardiac death due to ventricular tachyarrhythmias.
Gillis AM; Hamilton RM; LeFeuvre CA
Can J Cardiol; 2000 Jun; 16 Suppl C():34C-40C. PubMed ID: 10887277
[No Abstract] [Full Text] [Related]
10. Long QT syndrome associated with syndactyly identified in females.
Marks ML; Trippel DL; Keating MT
Am J Cardiol; 1995 Oct; 76(10):744-5. PubMed ID: 7572644
[TBL] [Abstract][Full Text] [Related]
11. Unusual retrospective prenatal findings in a male newborn with Timothy syndrome type 1.
Corona-Rivera JR; Barrios-Prieto E; Nieto-García R; Bloise R; Priori S; Napolitano C; Bobadilla-Morales L; Corona-Rivera A; Zapata-Aldana E; Peña-Padilla C; Rivera-Vargas J; Chavana-Naranjo E
Eur J Med Genet; 2015; 58(6-7):332-5. PubMed ID: 25882468
[TBL] [Abstract][Full Text] [Related]
12. A multicentre study of patients with Timothy syndrome.
Walsh MA; Turner C; Timothy KW; Seller N; Hares DL; James AF; Hancox JC; Uzun O; Boyce D; Stuart AG; Brennan P; Sarton C; McGuire K; Newbury-Ecob RA; Mcleod K
Europace; 2018 Feb; 20(2):377-385. PubMed ID: 28371864
[TBL] [Abstract][Full Text] [Related]
13. Dynamic QT Changes in Long QT Syndrome Type 8.
Harada M; Suzuki H; Ohno S; Ozawa J; Saitoh A; Horie M
Circ J; 2019 Jun; 83(7):1614. PubMed ID: 30584231
[No Abstract] [Full Text] [Related]
14. Novel Gain-of-Function Variant in
Kelu Bisabu K; Zhao J; Mokrane AE; Segura É; Marsolais M; Grondin S; Naas E; Gagnon J; Cadrin-Tourigny J; Aguilar M; Mongeon FP; Talajic M; Parent L; Tadros R
Circ Genom Precis Med; 2020 Dec; 13(6):e003123. PubMed ID: 33191761
[No Abstract] [Full Text] [Related]
15. Novel Timothy syndrome mutation leading to increase in CACNA1C window current.
Boczek NJ; Miller EM; Ye D; Nesterenko VV; Tester DJ; Antzelevitch C; Czosek RJ; Ackerman MJ; Ware SM
Heart Rhythm; 2015 Jan; 12(1):211-9. PubMed ID: 25260352
[TBL] [Abstract][Full Text] [Related]
16. Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes.
Fukuyama M; Wang Q; Kato K; Ohno S; Ding WG; Toyoda F; Itoh H; Kimura H; Makiyama T; Ito M; Matsuura H; Horie M
Europace; 2014 Dec; 16(12):1828-37. PubMed ID: 24728418
[TBL] [Abstract][Full Text] [Related]
17. Prolonged QT and hypertrophic cardiomyopathy in two families with 10 sudden deaths.
Gupta PR; Somani PN; Avasthey P; Singh VP
J Assoc Physicians India; 1985 May; 33(5):353-5. PubMed ID: 4044501
[No Abstract] [Full Text] [Related]
18. Timothy syndrome-like condition with syndactyly but without prolongation of the QT interval.
Kosaki R; Ono H; Terashima H; Kosaki K
Am J Med Genet A; 2018 Jul; 176(7):1657-1661. PubMed ID: 29736926
[TBL] [Abstract][Full Text] [Related]
19. Congenital long QT syndrome and 2:1 atrioventricular block with a mutation of the SCN5A gene.
Miura M; Yamagishi H; Morikawa Y; Matsuoka R
Pediatr Cardiol; 2003; 24(1):70-2. PubMed ID: 12574983
[TBL] [Abstract][Full Text] [Related]
20. Sudden cardiac arrest during anesthesia in a 30-month-old boy with syndactyly: a case of genetically proven Timothy syndrome.
An HS; Choi EY; Kwon BS; Kim GB; Bae EJ; Noh CI; Choi JY; Park SS
J Korean Med Sci; 2013 May; 28(5):788-91. PubMed ID: 23678275
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
