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T Voit

Showing results (61-70 of 143) with videos related to

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European Journal of Pediatrics|May 1, 1991
Myopathy in Williams-Beuren syndromeT Voit, H Kramer, C Thomas, et al.
Neuropediatrics|August 1, 1994
Coisogenic all-plus-one immunization: a model for identifying missing proteins in null-mutant conditions. Antibodies to dystrophin in mdx mouse after transplantation of muscle from normal coisogenic donorR E Bittner, B Streubel, S Shorny, et al.
Lancet (London, England)|September 20, 1986
Horizontal transmission of HIV infection between two siblingsV Wahn, H H Kramer, T Voit, et al.
Neuropediatrics|August 1, 1992
Sudden loss of hearing and vestibular function, muscular weakness, and multiple white matter lesions in preschool childrenH G Lenard, T Voit, A Lamprecht, et al.
Revue Neurologique|June 1, 1994
Immunohistologic and electron microscopic abnormalities of desmin and dystrophin in familial cardiomyopathy and myopathyH H Goebel, T Voit, I Warlo, et al.
Acta Neuropathologica|July 6, 2004
Optico-cochleo-dentate degeneration associated with severe peripheral neuropathy and caused by peroxisomal D-bifunctional protein deficiencyJ M Schröder, V Hackel, R J A Wanders, et al.
Klinische Padiatrie|April 29, 2005
[Lectin-reactive alpha-fetoprotein in tyrosinaemia type I]U Baumann, V Duhme, I Knerr, et al.
American Journal of Human Genetics|November 1, 1996
Apparent autosomal recessive inheritance in families with proximal spinal muscular atrophy affecting individuals in two generationsS Rudnik-Schöneborn, K Zerres, E Hahnen, et al.
Neuropediatrics|May 1, 1987
Neurological manifestations in three German children with AIDSB Biggemann, T Voit, E Neuen, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1989
[Membrane changes in Duchenne/Becker muscular dystrophy: lectin binding and localization of dystrophin]T Voit, K Patel, C A Sewry, et al.
Pageof 15

Showing results (61-70 of 143) with videos related to

Sort By:
Pageof 15
European Journal of Pediatrics|May 1, 1991
Myopathy in Williams-Beuren syndromeT Voit, H Kramer, C Thomas, et al.
Neuropediatrics|August 1, 1994
Coisogenic all-plus-one immunization: a model for identifying missing proteins in null-mutant conditions. Antibodies to dystrophin in mdx mouse after transplantation of muscle from normal coisogenic donorR E Bittner, B Streubel, S Shorny, et al.
Lancet (London, England)|September 20, 1986
Horizontal transmission of HIV infection between two siblingsV Wahn, H H Kramer, T Voit, et al.
Neuropediatrics|August 1, 1992
Sudden loss of hearing and vestibular function, muscular weakness, and multiple white matter lesions in preschool childrenH G Lenard, T Voit, A Lamprecht, et al.
Revue Neurologique|June 1, 1994
Immunohistologic and electron microscopic abnormalities of desmin and dystrophin in familial cardiomyopathy and myopathyH H Goebel, T Voit, I Warlo, et al.
Acta Neuropathologica|July 6, 2004
Optico-cochleo-dentate degeneration associated with severe peripheral neuropathy and caused by peroxisomal D-bifunctional protein deficiencyJ M Schröder, V Hackel, R J A Wanders, et al.
Klinische Padiatrie|April 29, 2005
[Lectin-reactive alpha-fetoprotein in tyrosinaemia type I]U Baumann, V Duhme, I Knerr, et al.
American Journal of Human Genetics|November 1, 1996
Apparent autosomal recessive inheritance in families with proximal spinal muscular atrophy affecting individuals in two generationsS Rudnik-Schöneborn, K Zerres, E Hahnen, et al.
Neuropediatrics|May 1, 1987
Neurological manifestations in three German children with AIDSB Biggemann, T Voit, E Neuen, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1989
[Membrane changes in Duchenne/Becker muscular dystrophy: lectin binding and localization of dystrophin]T Voit, K Patel, C A Sewry, et al.
Pageof 15