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N N Herschkowitz

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Brain Research|February 28, 1973
Sulfatide synthesis in neurons: a defect in mice with a hereditary myelination disorderA Kohlschütter, N N Herschkowitz
Pediatric Research|November 1, 1974
Studies on the pathogenetic mechanism of I-cell disease in cultured fibroblastsU N Wiesmann, N N Herschkowitz
The Journal of Biological Chemistry|August 10, 1974
Sulfogalactosylsphingosine sulfatase. Characteristics of the enzyme and its deficiency in metachromatic leukodystrophy in human cultured skin fibroblastsY Eto, U Wiesmann, N N Herschkowitz
Journal of Neurochemistry|November 1, 1976
Chemical compositions of brain and myelin in two patients with multiple sulphatase deficiency (a variant form of metachromatic leukodystrophy)Y Eto, C Meier, N N Herschkowitz
Neuroscience|January 1, 1977
Arylsulfatase A in developing normal and jimpy miceT Burkart, U N Wiesmann, N N Herschkowitz
Biochemical and Biophysical Research Communications|October 27, 1975
Effect of chloroquine on cultured fibroblasts: release of lysosomal hydrolases and inhibition of their uptakeU N Wiesmann, S DiDonato, N N Herschkowitz
Acta Paediatrica Scandinavica|January 1, 1974
Mucolipidosis II (I-cell disease). A clinical and biochemical studyU N Wiesmann, F Vassella, N N Herschkowitz
Acta Paediatrica Scandinavica|May 1, 1972
Correction of the defective sulfatide degradation in cultured fibroblasts from patients with metachromatic leucodystrophyU N Wiesmann, E E Rossi, N N Herschkowitz
Journal of Neurochemistry|December 1, 1974
Enzymic studies of sulphatases in tissues of the normal human and in metachromatic leukodystrophy with multiple sulphatase deficiencies: arylsulphatases A, B and C, cerebroside sulphatase, psychosine sulphatase and steroid sulphatasesY Eto, S Rampini, U Wiesmann, et al.
The New England Journal of Medicine|March 25, 1971
Treatment of metachromatic leukodystrophy in fibroblasts by enzyme replacementU N Wiesmann, E E Rossi, N N Herschkowitz
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Brain Research|February 28, 1973
Sulfatide synthesis in neurons: a defect in mice with a hereditary myelination disorderA Kohlschütter, N N Herschkowitz
Pediatric Research|November 1, 1974
Studies on the pathogenetic mechanism of I-cell disease in cultured fibroblastsU N Wiesmann, N N Herschkowitz
The Journal of Biological Chemistry|August 10, 1974
Sulfogalactosylsphingosine sulfatase. Characteristics of the enzyme and its deficiency in metachromatic leukodystrophy in human cultured skin fibroblastsY Eto, U Wiesmann, N N Herschkowitz
Journal of Neurochemistry|November 1, 1976
Chemical compositions of brain and myelin in two patients with multiple sulphatase deficiency (a variant form of metachromatic leukodystrophy)Y Eto, C Meier, N N Herschkowitz
Neuroscience|January 1, 1977
Arylsulfatase A in developing normal and jimpy miceT Burkart, U N Wiesmann, N N Herschkowitz
Biochemical and Biophysical Research Communications|October 27, 1975
Effect of chloroquine on cultured fibroblasts: release of lysosomal hydrolases and inhibition of their uptakeU N Wiesmann, S DiDonato, N N Herschkowitz
Acta Paediatrica Scandinavica|January 1, 1974
Mucolipidosis II (I-cell disease). A clinical and biochemical studyU N Wiesmann, F Vassella, N N Herschkowitz
Acta Paediatrica Scandinavica|May 1, 1972
Correction of the defective sulfatide degradation in cultured fibroblasts from patients with metachromatic leucodystrophyU N Wiesmann, E E Rossi, N N Herschkowitz
Journal of Neurochemistry|December 1, 1974
Enzymic studies of sulphatases in tissues of the normal human and in metachromatic leukodystrophy with multiple sulphatase deficiencies: arylsulphatases A, B and C, cerebroside sulphatase, psychosine sulphatase and steroid sulphatasesY Eto, S Rampini, U Wiesmann, et al.
The New England Journal of Medicine|March 25, 1971
Treatment of metachromatic leukodystrophy in fibroblasts by enzyme replacementU N Wiesmann, E E Rossi, N N Herschkowitz
Pageof 3