V Schuster|H W Kreth - JoVE Visualize

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Klinische Padiatrie|September 17, 2005

[Gianotti-Crosti syndrome in an infant following immunization]N Schwerk, C Schwerk, L Vogler, et al.

Human Genetics|April 1, 1995

Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8qO Steinlein, V Schuster, C Fischer, et al.

Klinische Padiatrie|May 12, 2006

Decreased factor XIII activity during severe Henoch-Schoenlein purpura -- does it play a role?F Prenzel, R Pfäffle, F Thiele, et al.

Prenatal Diagnosis|June 9, 1999

Prenatal diagnosis in a family with severe type I plasminogen deficiency, ligneous conjunctivitis and congenital hydrocephalusV Schuster, S Seidenspinner, C Müller, et al.

Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 25, 2000

Ligneous conjunctivitis in a girl with severe type I plasminogen deficiencyJ Kraft, W Lieb, P Zeitler, et al.

Infection|July 1, 1993

Serum concentrations of interferon gamma, interleukin-6 and neopterin in patients with infectious mononucleosis and other Epstein-Barr virus-related lymphoproliferative diseasesV Schuster, M Herold, H Wachter, et al.

Klinische Padiatrie|May 1, 1996

[Indirect genotype analysis in 2 families with early manifestation of autosome dominant polycystic nephropathy]V Schuster, S Uhlhaas, A E Horwitz, et al.

European Journal of Pediatrics|June 1, 1990

Effects of highly overdosed indomethacin in a preterm infant with symptomatic patent ductus arteriosusV Schuster, H B von Stockhausen, H W Seyberth

Annals of Neurology|April 1, 1992

Human immunodeficiency virus infection in microglia: correlation between cells infected in the brain and cells cultured from infectious brain tissueR Brinkmann, A Schwinn, O Narayan, et al.

Experimental Hematology|March 25, 1999

Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous diseaseJ Roesler, S Heyden, M Burdelski, et al.

Pageof 11

Showing results (61-70 of 105) with videos related to

Sort By:

Pageof 11

Klinische Padiatrie|September 17, 2005

[Gianotti-Crosti syndrome in an infant following immunization]N Schwerk, C Schwerk, L Vogler, et al.

Human Genetics|April 1, 1995

Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8qO Steinlein, V Schuster, C Fischer, et al.

Klinische Padiatrie|May 12, 2006

Decreased factor XIII activity during severe Henoch-Schoenlein purpura -- does it play a role?F Prenzel, R Pfäffle, F Thiele, et al.

Prenatal Diagnosis|June 9, 1999

Prenatal diagnosis in a family with severe type I plasminogen deficiency, ligneous conjunctivitis and congenital hydrocephalusV Schuster, S Seidenspinner, C Müller, et al.

Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 25, 2000

Ligneous conjunctivitis in a girl with severe type I plasminogen deficiencyJ Kraft, W Lieb, P Zeitler, et al.

Infection|July 1, 1993

Klinische Padiatrie|May 1, 1996

[Indirect genotype analysis in 2 families with early manifestation of autosome dominant polycystic nephropathy]V Schuster, S Uhlhaas, A E Horwitz, et al.

European Journal of Pediatrics|June 1, 1990

Effects of highly overdosed indomethacin in a preterm infant with symptomatic patent ductus arteriosusV Schuster, H B von Stockhausen, H W Seyberth

Annals of Neurology|April 1, 1992

Human immunodeficiency virus infection in microglia: correlation between cells infected in the brain and cells cultured from infectious brain tissueR Brinkmann, A Schwinn, O Narayan, et al.

Experimental Hematology|March 25, 1999

Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous diseaseJ Roesler, S Heyden, M Burdelski, et al.

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