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U N Wiesmann

Showing results (1-10 of 90) with videos related to

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Bulletin Der Schweizerischen Akademie Der Medizinischen Wissenschaften|March 1, 1978
[Pathophysiology of sulfatide metabolism in metachromatic leukodystrophy]U N Wiesmann
European Journal of Pediatrics|January 1, 1995
Forty years of paediatric research in inborn errors of metabolismU N Wiesmann
Helvetica Paediatrica Acta|April 1, 1974
Mild form of the Hunter syndrome, indentity of the biochemical defect with the severe typeU N Wiesmann, S Rampini
Developmental Biology|April 1, 1987
Sulfated glycosaminoglycans (GAG) in the developing mouse brain. Quantitative aspects on the metabolism of total and individual sulfated GAG in vivoT Burkart, U N Wiesmann
Advances in Experimental Medicine and Biology|January 1, 1980
Sialidoses (mucolipidoses), clinical picturesU N Wiesmann, N Herschkowitz
Biochemistry and Experimental Biology|January 1, 1977
Enzyme--cell membrane recognition (what we can learn from rare genetic lysosomal disorders)U N Wiesmann, S Di Donato
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1982
[Concepts of lysosomal storage disease--known facts and hypotheses]M A Spycher, U N Wiesmann
Helvetica Paediatrica Acta|May 1, 1975
Confirming by electron microscopy a prenatally diagnosed storage disorder: a note of cautionM A Spycher, U N Wiesmann
Pediatric Research|November 1, 1974
Studies on the pathogenetic mechanism of I-cell disease in cultured fibroblastsU N Wiesmann, N N Herschkowitz
Biochimica Et Biophysica Acta|October 11, 1983
Synthesis and subcellular transport of sulfogalactosyl glycerolipids in the myelinating mouse brainT Burkart, L Caimi, U N Wiesmann
Pageof 9

Showing results (1-10 of 90) with videos related to

Sort By:
Pageof 9
Bulletin Der Schweizerischen Akademie Der Medizinischen Wissenschaften|March 1, 1978
[Pathophysiology of sulfatide metabolism in metachromatic leukodystrophy]U N Wiesmann
European Journal of Pediatrics|January 1, 1995
Forty years of paediatric research in inborn errors of metabolismU N Wiesmann
Helvetica Paediatrica Acta|April 1, 1974
Mild form of the Hunter syndrome, indentity of the biochemical defect with the severe typeU N Wiesmann, S Rampini
Developmental Biology|April 1, 1987
Sulfated glycosaminoglycans (GAG) in the developing mouse brain. Quantitative aspects on the metabolism of total and individual sulfated GAG in vivoT Burkart, U N Wiesmann
Advances in Experimental Medicine and Biology|January 1, 1980
Sialidoses (mucolipidoses), clinical picturesU N Wiesmann, N Herschkowitz
Biochemistry and Experimental Biology|January 1, 1977
Enzyme--cell membrane recognition (what we can learn from rare genetic lysosomal disorders)U N Wiesmann, S Di Donato
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1982
[Concepts of lysosomal storage disease--known facts and hypotheses]M A Spycher, U N Wiesmann
Helvetica Paediatrica Acta|May 1, 1975
Confirming by electron microscopy a prenatally diagnosed storage disorder: a note of cautionM A Spycher, U N Wiesmann
Pediatric Research|November 1, 1974
Studies on the pathogenetic mechanism of I-cell disease in cultured fibroblastsU N Wiesmann, N N Herschkowitz
Biochimica Et Biophysica Acta|October 11, 1983
Synthesis and subcellular transport of sulfogalactosyl glycerolipids in the myelinating mouse brainT Burkart, L Caimi, U N Wiesmann
Pageof 9