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Neuropediatrics
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April 12, 2005
Congenital hydrocephalus as a rare association with ligneous conjunctivitis and type I plasminogen deficiency
A 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 probes
Nathaniel 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 study
T 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 susceptibility
Jie 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 conjunctivitis
V 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 childhood
Philip 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 immunodeficiency
V 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 mutations
E Jakkula, J Lohiniva, A Capone, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 89) with videos related to
Sort By:
Page
of 9
Neuropediatrics
|
April 12, 2005
Congenital hydrocephalus as a rare association with ligneous conjunctivitis and type I plasminogen deficiency
A 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 probes
Nathaniel 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 study
T 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 susceptibility
Jie 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 conjunctivitis
V 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 childhood
Philip 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 immunodeficiency
V 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 mutations
E Jakkula, J Lohiniva, A Capone, et al.
Page
of 9