Mutation of ALMS1 , a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome von Walker, Mark, Wilson, David I, Hearn, Tom, Renforth, Glenn L, Spalluto, Cosma, Hanley, Neil A, Piper, Karen, Brickwood, Sarah, White, Chris, Connolly, Vincent, Taylor, James F.N, Russell-Eggitt, Isabelle, Bonneau, Dominique

Volltext

Subdiaphragmatic venous hemodynamics in the Fontan circulation von Hsia, Tain-Yen, Khambadkone, Sachin, Deanfield, John E., Taylor, James F.N., Migliavacca, Francesco, de Leval, Marc R.

Volltext

Alström syndrome: Report of 22 cases and literature review von Russell-Eggitt, Isabelle M, Clayton, Peter T, Coffey, Rebecca, Kriss, Anthony, Taylor, David S.I, Taylor, James F.N

Volltext

IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome von Tyson, Jessica, Tranebjærg, Lisbeth, Bellman, Sue, Wren, Christopher, Taylor, James F.N., Bathen, Jørn, Aslaksen, Bjørn, Sørland, Svein Jan, Lund, Ole, Malcolm, Sue, Pembrey, Marcus, Bhattacharya, Shømi, Bitner-Glindzicz, Maria

Volltext

Evaluation of long-term results of homograft and heterograft valves in extracardiac conduits von Bull, C, Macartney, FJ, Horvath, P, Almeida, R, Merrill, W, Douglas, J, Taylor, JF, de Leval, MR, Stark, J

Volltext

Surgical technique to reduce the risks of heart block following closure of ventricular septal defect in atrioventricular discordance von de Leval, MR, Bastos, P, Stark, J, Taylor, JF, Macartney, FJ, Anderson, RH

Volltext

Alström syndrome von Russell-Eggitt, Isabelle M, Clayton, Peter T, Coffey, Rebecca, Kriss, Anthony, Taylor, David S.I, Taylor, James F.N

Volltext

Late outcome of survivors of intervention for neonatal aortic valve stenosis von Gaynor, J. William, Bull, Catherine, Sullivan, Ian D., Armstrong, Brenda E., Deanfield, John E., Taylor, James F.N., Rees, Philip G., Ungerleider, Ross M., de Leval, Marc R., Stark, Jaroslav, Elliott, Martin J.

Volltext

Vascular access in previously catheterised children and adolescents: a prospective study of 131 consecutive cases von Celermajer, D S, Robinson, J T, Taylor, J F

Volltext

Concurrent vascular ring and occult left pulmonary artery associated with ventricular septal defect: A report of an uncommon constellation von Dagar, Kulbhushan Singh, Hsia, Tain-Yen, Yates, Robert, Taylor, James F.N., de Leval, Marc R., Tsang, Victor

Volltext

Right atrial reduction for tachyarrhythmias in Ebstein's anomaly in infancy von Ahel, V, Kilvain, S, Rozmanić, V, Taylor, J F, Vukas, D

Volltext

Balloon dilation of pulmonary venous pathway obstruction after mustard repair for transposition of the great arteries von Cooper, Stephen G., Sullivan, Ian D., Bull, Catherine, Taylor, James F.N.

Volltext

Use of a subpulmonary ventricular chamber in the Fontan circulation von Bull, C, de Leval, MR, Stark, J, Taylor, JF, Macartney, FJ

Volltext

Management of critical aortic stenosis in infancy von Sink, JD, Smallhorn, JF, Macartney, FJ, Taylor, JF, Stark, J, de Leval, MR

Volltext

Long-term results of the “Palliative” mustard operation von Dhasmana, Janardan P., Stark, Jaroslav, de Leval, Marc, Macartney, Fergus J., Rees, Philip G., Taylor, James F.N.

Volltext

Postoperative Angiographic Assessment of Modified Blalock-Taussig Shunts Using Expanded Polytetrafluoroethylene (Gore-Tex) von McKay, Roxane, de Leval, Marc R., Rees, Philip, Taylor, James F.N., Macartney, Fergus J., Stark, Jaroslav

Volltext

Cardiac defects in the Hallerman-Streiff syndrome von Dinwiddie, Robert, Gewitz, Michael, Taylor, James F.N.

Volltext

Haemodynamics after Mustard's operation for transposition of the great arteries von Silove, E D, Taylor, J F

Volltext

Tricuspid atresia. Clinical course in 62 cases (1967--1974) von Patel, R, Fox, K, Taylor, J F, Graham, G R

Volltext

Absent right atrioventricular connection and double-inlet ventricle due to an unbalanced familial 8:13 chromosome translocation: a cautionary tale von Burn, J, Baraitser, M, Hughes, D T, Saldana-Garcia, P, Taylor, J F

Volltext