SCOPUS 정보 검색 플랫폼

Pediatric Cardiology

Volumn 29, Issue 6, 2008, Pages 1131-1132

Antenatal presentation of congenital long QT syndrome: A prenatal diagnosis not to be missed

(2) Baruteau, Alban Elouen a Schleich, Jean Marc a

a PONTCHAILLOU UNIVERSITY HOSPITAL (France)

Author keywords

[No Author keywords available]

Indexed keywords

BETA ADRENERGIC RECEPTOR BLOCKING AGENT;

ATRIOVENTRICULAR BLOCK; BRADYCARDIA; CLINICAL ASSESSMENT; CLINICAL FEATURE; DISEASE ASSOCIATION; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAM; FETUS WASTAGE; GENE MUTATION; HEART RATE VARIABILITY; HEART VENTRICLE ARRHYTHMIA; HUMAN; LETTER; LONG QT SYNDROME; MAGNETOCARDIOGRAPHY; PREGNANCY; PRENATAL DIAGNOSIS; RESUSCITATION; SUDDEN INFANT DEATH SYNDROME;

ADRENERGIC BETA-ANTAGONISTS; FEMALE; HUMANS; LONG QT SYNDROME; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 58549097651 PISSN: 01720643 EISSN: None Source Type: Journal
DOI: 10.1007/s00246-008-9271-7 Document Type: Letter

Times cited : (10)

References (13)

1
- 33846046495
- Prevalence of long-QT syndrome gene variants in sudden infant death syndrome
- M Arnestad L Crotti TO Rognum 2007 Prevalence of long-QT syndrome gene variants in sudden infant death syndrome Circulation 115 361 367
- (2007) Circulation , vol.115 , pp. 361-367
- Arnestad, M.¹ Crotti, L.² Rognum, T.O.³

2
- 40849097481
- Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation
- ZA Bhuiyan TS Momenah Q Gong 2008 Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation Heart Rhythm 5 553 561
- (2008) Heart Rhythm , vol.5 , pp. 553-561
- Bhuiyan, Z.A.¹ Momenah, T.S.² Gong, Q.³

3
- 0036936530
- Prenatal diagnosis and treatment of fetal long QT syndrome: A case report
- IK Chang MK Shyu CN Lee 2002 Prenatal diagnosis and treatment of fetal long QT syndrome: a case report Prenat Diagn 22 1209 1212
- (2002) Prenat Diagn , vol.22 , pp. 1209-1212
- Chang, I.K.¹ Shyu, M.K.² Lee, C.N.³

4
- 34548748598
- Sustained fetal bradycardia with 1:1 atrioventricular conduction and long QT syndrome
- JC Collazos RJ Acherman IH Law 2007 Sustained fetal bradycardia with 1:1 atrioventricular conduction and long QT syndrome Prenat Diagn 27 879 881
- (2007) Prenat Diagn , vol.27 , pp. 879-881
- Collazos, J.C.¹ Acherman, R.J.² Law, I.H.³

5
- 0032693508
- Fetal presentation of congenital long QT syndrome
- MT Donofrio SD Gullquist NG O'Connell FO Redwine 1999 Fetal presentation of congenital long QT syndrome Pediatr Cardiol 20 441 444
- (1999) Pediatr Cardiol , vol.20 , pp. 441-444
- Donofrio, M.T.¹ Gullquist, S.D.² O'Connell, N.G.³ Redwine, F.O.⁴

6
- 39749169764
- Magnetocardiographic demonstration of torsade de pointes in a fetus with congenital long QT syndrome
- H Horigome H Iwashita M Yoshinaga W Shimizu 2008 Magnetocardiographic demonstration of torsade de pointes in a fetus with congenital long QT syndrome J Cardiovasc Electrophysiol 19 334 335
- (2008) J Cardiovasc Electrophysiol , vol.19 , pp. 334-335
- Horigome, H.¹ Iwashita, H.² Yoshinaga, M.³ Shimizu, W.⁴

7
- 36048981858
- Inherited arrhythmias: A National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function
- SE Lehnart MJ Ackerman DW Benson Jr 2007 Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function Circulation 116 2325 2345
- (2007) Circulation , vol.116 , pp. 2325-2345
- Lehnart, S.E.¹ Ackerman, M.J.² Benson Jr., D.W.³

8
- 3042611768
- Recurrent third-trimester fetal loss and maternal mosaicism for long-QT syndrome
- TE Miller E Estrella RJ Myerburg 2004 Recurrent third-trimester fetal loss and maternal mosaicism for long-QT syndrome Circulation 109 3029 3034
- (2004) Circulation , vol.109 , pp. 3029-3034
- Miller, T.E.¹ Estrella, E.² Myerburg, R.J.³

9
- 38049146378
- Clinical practice: Long-QT syndrome
- DM Roden 2008 Clinical practice: long-QT syndrome N Engl J Med 358 169 176
- (2008) N Engl J Med , vol.358 , pp. 169-176
- Roden, D.M.¹

10
- 33644839159
- Images in cardiovascular medicine: Magnetocardiography in a fetus with long-QT syndrome
- L Schmitz M Burghoff 2005 Images in cardiovascular medicine: magnetocardiography in a fetus with long-QT syndrome Circulation 112 e68 e69
- (2005) Circulation , vol.112
- Schmitz, L.¹ Burghoff, M.²

11
- 17144450747
- Prolongation of the QT interval and the sudden infant death syndrome
- PJ Schwartz M Stramba-Badiale A Segantini 1998 Prolongation of the QT interval and the sudden infant death syndrome N Engl J Med 338 1709 1714
- (1998) N Engl J Med , vol.338 , pp. 1709-1714
- Schwartz, P.J.¹ Stramba-Badiale, M.² Segantini, A.³

12
- 4043121130
- Low incidence of cardiac events with beta-blocking therapy in children with long QT syndrome
- E Villain I Denjoy JM Lupoglazoff 2004 Low incidence of cardiac events with beta-blocking therapy in children with long QT syndrome Eur Heart J 25 1405 1411
- (2004) Eur Heart J , vol.25 , pp. 1405-1411
- Villain, E.¹ Denjoy, I.² Lupoglazoff, J.M.³

13
- 0035806944
- De novo mutation in the SCN5A gene associated with early onset of sudden infant death
- H Wedekind JP Smits E Schulze-Bahr 2001 De novo mutation in the SCN5A gene associated with early onset of sudden infant death Circulation 104 1158 1164
- (2001) Circulation , vol.104 , pp. 1158-1164
- Wedekind, H.¹ Smits, J.P.² Schulze-Bahr, E.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.