Current treatment and prognosis in children with functionally univentricular hearts

Por Kaulitz, R, Hofbeck, M
Publicado em 2005

Improved visualisation of a coronary artery fistula by the "laid-back" aortogram.

Por Hofbeck, M, Wild, F, Singer, H
Publicado em 1993

Thrombolysis of a modified Blalock-Taussig shunt with recombinant tissue plasminogen activator in a newborn infant with pulmonary atresia and ventricular septal defect.

Por Ries, M, Singer, H, Hofbeck, M
Publicado em 1994

Tissue plasminogen activator (alteplase) treatment for femoral artery thrombosis after cardiac catheterisation in infants and children.

Por Ries, M, Singer, H, Hofbeck, M, Klinge, J
Publicado em 1994

Frequency of stress lesions of the upper gastrointestinal tract in paediatric patients after cardiac surgery: effects of prophylaxis.

Por Behrens, R, Hofbeck, M, Singer, H, Scharf, J, Rupprecht, T
Publicado em 1994

Prenatal findings in patients with prolonged QT interval in the neonatal period.

Por Hofbeck, M., Ulmer, H., Beinder, E., Sieber, E., Singer, H.
Publicado em 1997

Acquired von Willebrand syndrome in children with patent ductus arteriosus

Por Rauch, R, Budde, U, Koch, A, Girisch, M, Hofbeck, M
Publicado em 2002

A novel 22q11.2 microdeletion in DiGeorge syndrome.

Por Rauch, A, Pfeiffer, R A, Leipold, G, Singer, H, Tigges, M, Hofbeck, M
Publicado em 1999

Changes in pulmonary artery size before and after total cavopulmonary connection

Por Buheitel, G., Hofbeck, M., Tenbrink, U., Leipold, G., von der Emde, J., Singer, H.
Publicado em 1997

Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries

Por Hofbeck, M., Rauch, A., Buheitel, G., Leipold, G., von der Emde, J., Pfeiffer, R., Singer, H.
Publicado em 1998

Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients

Por Rauch, A, Devriendt, K, Koch, A, Rauch, R, Gewillig, M, Kraus, C, Weyand, M, Singer, H, Reis, A, Hofbeck, M
Publicado em 2004

Systematic assessment of atypical deletions reveals genotype–phenotype correlation in 22q11.2

Por Rauch, A, Zink, S, Zweier, C, Thiel, C, Koch, A, Rauch, R, Lascorz, J, Huffmeier, U, Weyand, M, Singer, H, Hofbeck, M
Publicado em 2005