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M Cantz

Showing results (51-60 of 72) with videos related to

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American Journal of Medical Genetics|May 3, 1996
Methylamine accumulation in cultured cells as a measure of the aqueous storage compartment in the laboratory diagnosis of genetic lysosomal diseasesJ Kopitz, K Harzer, A Kohlschütter, et al.
Fetal Diagnosis and Therapy|March 1, 1996
Nonimmune hydrops fetalis with galactosialidosis: consequences for family planningF Haverkamp, D Jacobs, M Cantz, et al.
Experimental Cell Research|December 1, 1984
Pattern of collagen synthesis and chemotactic response of fibroblasts derived from mucopolysaccharidosis patientsB F Pontz, A Albini, H Mensing, et al.
Biochemical and Biophysical Research Communications|March 5, 1971
Biochemical heterogeneity of the Sanfilippo syndrome: preliminary characterization of two deficient factorsH Kresse, U Wiesmann, M Cantz, et al.
Neuropediatrics|May 1, 1985
Familial lysosomal storage disease with generalized vacuolization and sialic aciduria. Sporadic Salla diseaseK Wolburg-Buchholz, W Schlote, J Baumkötter, et al.
Acta Paediatrica Belgica|April 1, 1976
Clinical ultrastructural and tissue culture studies in a possible compound Hurler-Scheie caseM Tondeur, E Vamos-Hurwitz, M Cantz, et al.
FEBS Letters|July 27, 2001
Splice donor site mutation in the lysosomal neuraminidase gene causing exon skipping and complete loss of enzyme activity in a sialidosis patientR Penzel, J Uhl, J Kopitz, et al.
Neurology|November 10, 2004
Adult alpha-mannosidosis: clinical progression in the absence of demyelinationA Gutschalk, I Harting, M Cantz, et al.
Der Nervenarzt|March 11, 2005
[Unusual course of alpha-mannosidosis with symptoms of paranoid-hallucinatory psychosis]U Seidl, F L Giesel, M Cantz, et al.
Human Genetics|January 1, 1985
N-Acetylneuraminic acid storage diseaseJ Baumkötter, M Cantz, K Mendla, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics|May 3, 1996
Methylamine accumulation in cultured cells as a measure of the aqueous storage compartment in the laboratory diagnosis of genetic lysosomal diseasesJ Kopitz, K Harzer, A Kohlschütter, et al.
Fetal Diagnosis and Therapy|March 1, 1996
Nonimmune hydrops fetalis with galactosialidosis: consequences for family planningF Haverkamp, D Jacobs, M Cantz, et al.
Experimental Cell Research|December 1, 1984
Pattern of collagen synthesis and chemotactic response of fibroblasts derived from mucopolysaccharidosis patientsB F Pontz, A Albini, H Mensing, et al.
Biochemical and Biophysical Research Communications|March 5, 1971
Biochemical heterogeneity of the Sanfilippo syndrome: preliminary characterization of two deficient factorsH Kresse, U Wiesmann, M Cantz, et al.
Neuropediatrics|May 1, 1985
Familial lysosomal storage disease with generalized vacuolization and sialic aciduria. Sporadic Salla diseaseK Wolburg-Buchholz, W Schlote, J Baumkötter, et al.
Acta Paediatrica Belgica|April 1, 1976
Clinical ultrastructural and tissue culture studies in a possible compound Hurler-Scheie caseM Tondeur, E Vamos-Hurwitz, M Cantz, et al.
FEBS Letters|July 27, 2001
Splice donor site mutation in the lysosomal neuraminidase gene causing exon skipping and complete loss of enzyme activity in a sialidosis patientR Penzel, J Uhl, J Kopitz, et al.
Neurology|November 10, 2004
Adult alpha-mannosidosis: clinical progression in the absence of demyelinationA Gutschalk, I Harting, M Cantz, et al.
Der Nervenarzt|March 11, 2005
[Unusual course of alpha-mannosidosis with symptoms of paranoid-hallucinatory psychosis]U Seidl, F L Giesel, M Cantz, et al.
Human Genetics|January 1, 1985
N-Acetylneuraminic acid storage diseaseJ Baumkötter, M Cantz, K Mendla, et al.
Pageof 8