R. Rauch

发表

Genotype-phenotype correlations in Noonan syndrome.

W. Kress, M. Zenker, A. Reis, 2004, The Journal of pediatrics.

Effects of closed-loop automatic control of the inspiratory fraction of oxygen (FiO2-C) on outcome of extremely preterm infants – study protocol of a randomized controlled parallel group multicenter trial for safety and efficacy

A. Hübler, C. Poets, B. Bohnhorst, 2019, BMC Pediatrics.

Does obesity affect the non-invasive measurement of cardiac output performed by electrical cardiometry in children and adolescents?

K. Norozi, Michael R. Miller, R. Rauch, 2018, Journal of Clinical Monitoring and Computing.

Comprehensive genotype–phenotype analysis in 230 patients with tetralogy of Fallot

A. Rauch, C. Zweier, J. Hoyer, 2009, Journal of Medical Genetics.

Comprehensive genotype e phenotype analysis in 230 patients with tetralogy of Fallot

A. Rauch, C. Zweier, J. Hoyer, 2022 .

Anterosuperior Diverticula of the Right Ventricle: Morphological Spectrum and Long-Term Outcome of a Distinct Cardiac Anomaly

M. Hofbeck, H. Singer, R. Rauch, 2014, Pediatric Cardiology.

Acquired von Willebrand syndrome in children with patent ductus arteriosus

M. Hofbeck, R. Rauch, A. Koch, 2002, Heart.

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

M. Weyand, C. Thiel, A. Rauch, 2005, Journal of Medical Genetics.

Persistent high factor VIII:C in a child with ischemic stroke.

M. Hofbeck, R. Rauch, J. Klinge, 2003, Thrombosis research.

Prophylaxis of thromboembolic complications after the Fontan operation (total cavopulmonary anastomosis).

A. Wessel, M. Hofbeck, H. Bertram, 2005, The Journal of thoracic and cardiovascular surgery.

Bleeding diathesis in Noonan syndrome: is acquired von Willebrand syndrome the clue?

M. Zenker, M. Hofbeck, R. Rauch, 2012, Thrombosis research.

[A life-threatening cardiomyopathy following port-a-cath infection under immune tolerance therapy].

M. Hofbeck, R. Rauch, G. Wiegand, 2007, Hamostaseologie.

Refractory bleeding following major surgery of a giant sacrococcygeal teratoma in a premature infant: successful use of recombinant factor VIIa

M. Hofbeck, R. Carbon, R. Rauch, 2004, European Journal of Pediatrics.

Aminoterminal Pro B-Type Natriuretic Peptide (NT-proBNP) Levels for Monitoring Interventions in Paediatric Cardiac Patients with Stenotic Lesions

K. Norozi, K. Kleesiek, G. Filler, 2010, International journal of pediatrics.

Residual platelet reactivity after aspirin administration in pediatric patients.

M. Gawaz, D. Stakos, M. Hofbeck, 2010, Thrombosis research.

Non-invasive measurement of cardiac output in obese children and adolescents: comparison of electrical cardiometry and transthoracic Doppler echocardiography

K. Norozi, G. Filler, T. Robinson, 2013, Journal of Clinical Monitoring and Computing.

Emergency correction of coagulation for mitral valve replacement in an orally anticoagulated 17-year-old patient with pronounced hepatic dysfunction

M. Hofbeck, H. Singer, R. Rauch, 1999, Intensive Care Medicine.

Factor X deficiency and intracranial bleeding: who is at risk?

M. Hofbeck, K. Wulff, R. Rauch, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays

A. Ekici, F. Rüschendorf, C. Becker, 2007, Journal of Medical Genetics.

Search for somatic 22q11.2 deletions in patients with conotruncal heart defects

M. Weyand, A. Rauch, G. Buheitel, 2004, American journal of medical genetics. Part A.

Recanalisation of bilateral superior vena cava after total cavopulmonary connection

M. Hofbeck, R. Kaulitz, G. Ziemer, 2005, Zeitschrift für Kardiologie.

Small coronary artery fistulae in childhood: a 6-year experience of 31 cases in a tertiary paediatric cardiac centre

K. Norozi, R. Rauch, E. Welisch, 2015, Cardiology in the Young.

Are the children and adolescents with congenital heart disease living in Southwestern Ontario really overweight and obese?

K. Norozi, J. Seabrook, R. Rauch, 2013, Cardiology in the Young.

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

K. Devriendt, M. Weyand, A. Reis, 2004, Journal of Medical Genetics.

A 2-year-old boy with recurrent severe bleeding: von Willebrand type 2B and ITP – or von Willebrand type 2B alone?

R. Schneppenheim, R. Rauch, U. Budde, 1999, European Journal of Pediatrics.

N-terminal pro-brain natriuretic peptide level as a screening tool for cardiac involvement in paediatric diseases of extracardiac origin

K. Norozi, R. Rauch, E. Welisch, 2011, Clinical Research in Cardiology.

Laterality of the aortic arch and anomalies of the subclavian artery—reliable indicators for 22q11.2 deletion syndromes?

A. Rauch, M. Hofbeck, H. Singer, 2004, European Journal of Pediatrics.

Title page. Pulmonary artery thrombosis in a premature infant.

M. Hofbeck, R. Kaulitz, R. Rauch, 2008, Ultraschall in der Medizin.

Cervical origin of the subclavian artery as a specific marker for monosomy 22q11.

A. Dufke, A. Rauch, M. Hofbeck, 2002, The American journal of cardiology.

[Salmonella enteritidis infection presenting with septic shock, renal failure and cutaneous manifestations].

M. Hofbeck, U. Heininger, R. Rauch, 2009, Klinische Padiatrie.

The Health Initiative Program for Kids (HIP Kids): effects of a 1-year multidisciplinary lifestyle intervention on adiposity and quality of life in obese children and adolescents - a longitudinal pilot intervention study

K. Norozi, J. Seabrook, G. Filler, 2014, BMC Pediatrics.

[Cervical origin of the subclavian artery: echocardiographic diagnosis in patients with monosomy 22q11].

A. Rauch, M. Hofbeck, H. Singer, 2005, Ultraschall in der Medizin.

[Echocardiographic diagnosis of the aorto-left ventricular tunnel].

M. Hofbeck, R. Kaulitz, G. Ziemer, 2003, Ultraschall in der Medizin.

Hemostatic Changes following the Modified Fontan Operation (Total Cavopulmonary Connection)

G. Buheitel, M. Hofbeck, H. Singer, 2000, Thrombosis and Haemostasis.

Bleeding diathesis in Noonan syndrome: is acquired von Willebrand syndrome the clue?

M. Zenker, M. Hofbeck, R. Rauch, 2012, Thrombosis Research.