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V Schuster

Showing results (61-70 of 89) with videos related to

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European Journal of Pediatrics|June 1, 1994
Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative diseaseV Schuster, S Seidenspinner, T Grimm, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|April 6, 1999
Human homozygous type I plasminogen deficiency and ligneous conjunctivitisA M Mingers, A Philapitsch, P Zeitler, et al.
Klinische Padiatrie|November 6, 2009
Twenty year follow up of a patient with a new de-novo NLRP3 mutation (S595G) and CINCA syndromeM Kanariou, C Dracou, K Spanou, et al.
Infection|April 2, 2010
Lethal influenza B myocarditis in a child and review of the literature for pediatric age groupsH Frank, C Wittekind, U G Liebert, et al.
Klinische Padiatrie|January 15, 2016
[Evaluation and Utilization - Quality Management in a Paediatric University Outpatient Department]M Meier, J Brell, L Grieger, et al.
Klinische Padiatrie|September 1, 1995
[X-chromosome recessive lymphoproliferative disease (XLP): molecular genetic studies]V Schuster, T Grimm, W Kress, et al.
Pediatric Pulmonology|July 31, 2001
Pulmonary involvement in a child with ligneous conjunctivitis and homozygous type I plasminogen deficiencyU Ozçelik, Z Akçören, D Anadol, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 2013
Ligneous conjunctivitis in a young patient with homozygous K19E plasminogen gene mutation: a diagnostic and therapeutic challengeA Kuonen, J Vaudaux, M Hamedani, et al.
Klinische Padiatrie|November 17, 2005
[Viral infections in pediatric cancer patients]F R Schuster, A Simon, H-J Laws, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 1, 1991
Opioid receptor activity of GI 87084B, a novel ultra-short acting analgesic, in isolated tissuesM K James, P L Feldman, S V Schuster, et al.
Pageof 9

Showing results (61-70 of 89) with videos related to

Sort By:
Pageof 9
European Journal of Pediatrics|June 1, 1994
Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative diseaseV Schuster, S Seidenspinner, T Grimm, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|April 6, 1999
Human homozygous type I plasminogen deficiency and ligneous conjunctivitisA M Mingers, A Philapitsch, P Zeitler, et al.
Klinische Padiatrie|November 6, 2009
Twenty year follow up of a patient with a new de-novo NLRP3 mutation (S595G) and CINCA syndromeM Kanariou, C Dracou, K Spanou, et al.
Infection|April 2, 2010
Lethal influenza B myocarditis in a child and review of the literature for pediatric age groupsH Frank, C Wittekind, U G Liebert, et al.
Klinische Padiatrie|January 15, 2016
[Evaluation and Utilization - Quality Management in a Paediatric University Outpatient Department]M Meier, J Brell, L Grieger, et al.
Klinische Padiatrie|September 1, 1995
[X-chromosome recessive lymphoproliferative disease (XLP): molecular genetic studies]V Schuster, T Grimm, W Kress, et al.
Pediatric Pulmonology|July 31, 2001
Pulmonary involvement in a child with ligneous conjunctivitis and homozygous type I plasminogen deficiencyU Ozçelik, Z Akçören, D Anadol, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 2013
Ligneous conjunctivitis in a young patient with homozygous K19E plasminogen gene mutation: a diagnostic and therapeutic challengeA Kuonen, J Vaudaux, M Hamedani, et al.
Klinische Padiatrie|November 17, 2005
[Viral infections in pediatric cancer patients]F R Schuster, A Simon, H-J Laws, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 1, 1991
Opioid receptor activity of GI 87084B, a novel ultra-short acting analgesic, in isolated tissuesM K James, P L Feldman, S V Schuster, et al.
Pageof 9