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V Schuster

Showing results (71-80 of 89) with videos related to

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Neuropediatrics|April 12, 2005
Congenital hydrocephalus as a rare association with ligneous conjunctivitis and type I plasminogen deficiencyA T Aslan, U Ozcelik, D Dogru, et al.
Inorganic Chemistry|March 15, 2005
Coumarin-based chemosensors for zinc(II): toward the determination of the design algorithm for CHEF-type and ratiometric probesNathaniel C Lim, Jolene V Schuster, Maura C Porto, et al.
Lancet (London, England)|November 27, 2007
Efficacy of human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in European infants: randomised, double-blind controlled studyT Vesikari, A Karvonen, R Prymula, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|June 28, 2006
Longitudinal effects of pro-tobacco and anti-tobacco messages on adolescent smoking susceptibilityJie Wu Weiss, Steven Cen, Darleen V Schuster, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1993
[Treatment of secondary infections in symptomatic HIV-infections in childhood]V Wahn, B H Belohradsky, S Enenkel-Stoodt, et al.
Thrombosis and Haemostasis|July 4, 2001
Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitisV Schuster, P Zeitler, S Seregard, et al.
Monographs of the Society for Research in Child Development|January 16, 2004
The development of executive function in early childhoodPhilip David Zelazo, Ulrich Müller, Douglas Frye, et al.
European Journal of Pediatrics|November 1, 1990
Epstein-Barr virus infection rapidly progressing to monoclonal lymphoproliferative disease in a child with selective immunodeficiencyV Schuster, H W Kreth, H K Müller-Hermelink, et al.
Human Molecular Genetics|November 11, 1999
Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP)O Brandau, V Schuster, M Weiss, et al.
Journal of Medical Genetics|December 20, 2003
A recurrent R718W mutation in COMP results in multiple epiphyseal dysplasia with mild myopathy: clinical and pathogenetic overlap with collagen IX mutationsE Jakkula, J Lohiniva, A Capone, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
Neuropediatrics|April 12, 2005
Congenital hydrocephalus as a rare association with ligneous conjunctivitis and type I plasminogen deficiencyA T Aslan, U Ozcelik, D Dogru, et al.
Inorganic Chemistry|March 15, 2005
Coumarin-based chemosensors for zinc(II): toward the determination of the design algorithm for CHEF-type and ratiometric probesNathaniel C Lim, Jolene V Schuster, Maura C Porto, et al.
Lancet (London, England)|November 27, 2007
Efficacy of human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in European infants: randomised, double-blind controlled studyT Vesikari, A Karvonen, R Prymula, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|June 28, 2006
Longitudinal effects of pro-tobacco and anti-tobacco messages on adolescent smoking susceptibilityJie Wu Weiss, Steven Cen, Darleen V Schuster, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1993
[Treatment of secondary infections in symptomatic HIV-infections in childhood]V Wahn, B H Belohradsky, S Enenkel-Stoodt, et al.
Thrombosis and Haemostasis|July 4, 2001
Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitisV Schuster, P Zeitler, S Seregard, et al.
Monographs of the Society for Research in Child Development|January 16, 2004
The development of executive function in early childhoodPhilip David Zelazo, Ulrich Müller, Douglas Frye, et al.
European Journal of Pediatrics|November 1, 1990
Epstein-Barr virus infection rapidly progressing to monoclonal lymphoproliferative disease in a child with selective immunodeficiencyV Schuster, H W Kreth, H K Müller-Hermelink, et al.
Human Molecular Genetics|November 11, 1999
Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP)O Brandau, V Schuster, M Weiss, et al.
Journal of Medical Genetics|December 20, 2003
A recurrent R718W mutation in COMP results in multiple epiphyseal dysplasia with mild myopathy: clinical and pathogenetic overlap with collagen IX mutationsE Jakkula, J Lohiniva, A Capone, et al.
Pageof 9