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Ralf Rauch

Ralf Rauch,University of Tübingen,Family Medicine,Cardiology,Diseases

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Ralf Rauch

University of Tübingen

Publications: 50 | Citations: 238

Fields: Family Medicine, Cardiology, Diseases

Collaborated with 192 co-authors from 1991 to 2010 | Cited by 1100 authors

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Publications (50)

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Comprehensive genotype–phenotype analysis in 230 patients with tetralogy of Fallot (Citations: 5)

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Journal: Journal of Medical Genetics - J MED GENET , vol. 47, no. 5, pp. 321-331, 2010

Residual platelet reactivity after aspirin administration in pediatric patients

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Journal: Thrombosis Research - THROMB RES , vol. 126, no. 1, pp. e58-e60, 2010

Septischer Schock mit Niereninsuffizienz und Hautmanifestationen als Komplikation einer Salmonella-enteritidis-Infektion (Citations: 1)

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Journal: Klinische Padiatrie - KLIN PADIAT , vol. 221, no. 01, pp. 41-43, 2009

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

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Journal: International Journal of Pediatrics , vol. 2009, pp. 1-7, 2009

Dimenhydrinat-Intoxikation bei einem 3? Jahre alten Mädchen mit dilatativer Kardiomyopathie

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Journal: Klinische Padiatrie - KLIN PADIAT , vol. 221, no. 01, pp. 44-45, 2009

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Citations (238 times by 217 publications)

Reducing the startup time of aerobic granular sludge reactors through seeding floccular sludge with crushed aerobic granules (Citations: 1)

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Journal: Water Research - WATER RES , vol. 45, no. 16, pp. 5075-5083, 2011

Cerebrospinal fluid leakage—Reliable diagnostic methods

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Journal: Clinica Chimica Acta - CLIN CHIM ACTA , vol. 412, no. 11, pp. 837-840, 2011

The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

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Journal: Journal of Medical Genetics - J MED GENET , vol. 48, no. 6, pp. 396-406, 2011

Recombinant activated factor VIIa treatment for refractory hemorrhage in infants

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Journal: Journal of Perinatology - J PERINATOL , vol. 31, no. 3, pp. 188-192, 2011

Congenital stridor and wheezing as harbingers of the del22q11.2 syndrome presenting cardiovascular malformations of right aortic arch, aberrant left subclavian artery, Kommerell's diverticulum, and left ligamentum arteriosum

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Journal: Cardiovascular Pathology - CARDIOVASC PATHOL , vol. 20, no. 2, pp. 124-129, 2011

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