Results
|
41.
|
|
|
42.
|
|
|
43.
|
|
|
44.
|
|
|
45.
|
|
|
46.
|
|
|
47.
|
A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype. [electronic resource] by
- Schulze-Bahr, E
- Schwarz, M
- Hauenschild, S
- Wedekind, H
- Funke, H
- Haverkamp, W
- Breithardt, G
- Pongs, O
- Isbrandt, D
- Hoffman, S
Producer: 20020114
In:
Journal of molecular medicine (Berlin, Germany) vol. 79
Availability: No items available.
|
|
48.
|
Effective long-term control of cardiac events with beta-blockers in a family with a common LQT1 mutation. [electronic resource] by
- Wedekind, H
- Schwarz, M
- Hauenschild, S
- Djonlagic, H
- Haverkamp, W
- Breithardt, G
- Wülfing, T
- Pongs, O
- Isbrandt, D
- Schulze-Bahr, E
Producer: 20041122
In:
Clinical genetics vol. 65
Availability: No items available.
|
|
49.
|
|
|
50.
|
|
|
51.
|
[Clinical aspects and molecular genetics of the Jervell- and Lange-Nielsen Syndrome]. [electronic resource] by
- Mönnig, G
- Schulze-Bahr, E
- Wedekind, H
- Eckardt, L
- Kirchhof, P
- Funke, H
- Kotthoff, S
- Vogt, J
- Assmann, G
- Breithardt, G
- Haverkamp, W
Producer: 20021016
In:
Zeitschrift fur Kardiologie vol. 91
Availability: No items available.
|
|
52.
|
Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndrome. [electronic resource] by
- Moennig, G
- Schulze-Bahr, E
- Wedekind, H
- Borggrefe, M
- Funke, H
- Toelle, M
- Kirchhof, P
- Eckardt, L
- Assmann, G
- Breithardt, G
- Haverkamp, W
Producer: 20010927
In:
Pacing and clinical electrophysiology : PACE vol. 24
Availability: No items available.
|
|
53.
|
Molecular diagnosis in a child with sudden infant death syndrome. [electronic resource] by
- Schwartz, P J
- Priori, S G
- Bloise, R
- Napolitano, C
- Ronchetti, E
- Piccinini, A
- Goj, C
- Breithardt, G
- Schulze-Bahr, E
- Wedekind, H
- Nastoli, J
Producer: 20011204
In:
Lancet (London, England) vol. 358
Availability: No items available.
|
|
54.
|
C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence. [electronic resource] by
- Berthet, M
- Denjoy, I
- Donger, C
- Demay, L
- Hammoude, H
- Klug, D
- Schulze-Bahr, E
- Richard, P
- Funke, H
- Schwartz, K
- Coumel, P
- Hainque, B
- Guicheney, P
Producer: 19990414
In:
Circulation vol. 99
Availability: No items available.
|
|
55.
|
Electrophysiologic investigation in Brugada syndrome; yield of programmed ventricular stimulation at two ventricular sites with up to three premature beats. [electronic resource] by
- Eckardt, L
- Kirchhof, P
- Schulze-Bahr, E
- Rolf, S
- Ribbing, M
- Loh, P
- Bruns, H-J
- Witte, A
- Milberg, P
- Borggrefe, M
- Breithardt, G
- Wichter, T
- Haverkamp, W
Producer: 20021211
In:
European heart journal vol. 23
Availability: No items available.
|
|
56.
|
Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome. [electronic resource] by
- Chen, Q
- Zhang, D
- Gingell, R L
- Moss, A J
- Napolitano, C
- Priori, S G
- Schwartz, P J
- Kehoe, E
- Robinson, J L
- Schulze-Bahr, E
- Wang, Q
- Towbin, J A
Producer: 19990415
In:
Circulation vol. 99
Availability: No items available.
|
|
57.
|
De novo mutation in the SCN5A gene associated with early onset of sudden infant death. [electronic resource] by
- Wedekind, H
- Smits, J P
- Schulze-Bahr, E
- Arnold, R
- Veldkamp, M W
- Bajanowski, T
- Borggrefe, M
- Brinkmann, B
- Warnecke, I
- Funke, H
- Bhuiyan, Z A
- Wilde, A A
- Breithardt, G
- Haverkamp, W
Producer: 20011011
In:
Circulation vol. 104
Availability: No items available.
|
|
58.
|
KCNE1 mutations cause jervell and Lange-Nielsen syndrome. [electronic resource] by
- Schulze-Bahr, E
- Wang, Q
- Wedekind, H
- Haverkamp, W
- Chen, Q
- Sun, Y
- Rubie, C
- Hördt, M
- Towbin, J A
- Borggrefe, M
- Assmann, G
- Qu, X
- Somberg, J C
- Breithardt, G
- Oberti, C
- Funke, H
Producer: 19971204
In:
Nature genetics vol. 17
Availability: No items available.
|
|
59.
|
Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry. [electronic resource] by
- Probst, V
- Veltmann, C
- Eckardt, L
- Meregalli, P G
- Gaita, F
- Tan, H L
- Babuty, D
- Sacher, F
- Giustetto, C
- Schulze-Bahr, E
- Borggrefe, M
- Haissaguerre, M
- Mabo, P
- Le Marec, H
- Wolpert, C
- Wilde, A A M
Producer: 20100309
In:
Circulation vol. 121
Availability: No items available.
|
|
60.
|
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. [electronic resource] by
- Chen, Q
- Kirsch, G E
- Zhang, D
- Brugada, R
- Brugada, J
- Brugada, P
- Potenza, D
- Moya, A
- Borggrefe, M
- Breithardt, G
- Ortiz-Lopez, R
- Wang, Z
- Antzelevitch, C
- O'Brien, R E
- Schulze-Bahr, E
- Keating, M T
- Towbin, J A
- Wang, Q
Producer: 19980406
In:
Nature vol. 392
Availability: No items available.
|