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B W VOLK

Showing results (51-60 of 67) with videos related to

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Journal of the Neurological Sciences|May 1, 1973
Ophthalmoplegia plus with morphological and chemical studies of cerebellar and muscle tissueL Schneck, M Adachi, P Briet, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|March 1, 1970
Hexosaminidase activities in a case of systemic GM2 gangliosidosis of late infantile typeL Schneck, J Friedland, M Pourfar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1970
Identification of Tay-Sachs disease carriers by acrylamide gel electrophoresisJ Friedland, L Schneck, A Saifer, et al.
Advances in Experimental Medicine and Biology|January 1, 1976
Ultrastructure and biochemical studies of rat CNS and viscera after subcutaneous injection of chlorphentermineM Adachi, C Tsai, M Greenbaum, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|December 1, 1970
Early evolution of cytoplasmic inclusion bodies in Tay-Sachs diseaseB W Volk, M Adachi, J Friedland, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|April 1, 1971
Screening for Tay-Sachs disease in utero using amniotic fluidJ Friedland, G Perle, A Saifer, et al.
American Journal of Obstetrics and Gynecology|February 15, 1973
Caveats of antenatal diagnosis of Tay-Sachs diseaseA Saifer, L Schneck, G Perle, et al.
Neurology|October 1, 1974
Fabry's disease in a black man without skin lesionsB W Volk, L Schneck, J E Clemmons, et al.
Journal of Neurochemistry|March 1, 1970
Cerebral lipids in a case of systemic Gm2-gangliosidosis of a late infantile typeC Klibansky, A Saifer, N I Feldman, et al.
Pediatrics|August 1, 1973
The Tay-Sachs disease fibroblast model: failure to respond to exogenous hexosaminidase AL Schneck, D Amsterdam, S E Brooks, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
Journal of the Neurological Sciences|May 1, 1973
Ophthalmoplegia plus with morphological and chemical studies of cerebellar and muscle tissueL Schneck, M Adachi, P Briet, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|March 1, 1970
Hexosaminidase activities in a case of systemic GM2 gangliosidosis of late infantile typeL Schneck, J Friedland, M Pourfar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1970
Identification of Tay-Sachs disease carriers by acrylamide gel electrophoresisJ Friedland, L Schneck, A Saifer, et al.
Advances in Experimental Medicine and Biology|January 1, 1976
Ultrastructure and biochemical studies of rat CNS and viscera after subcutaneous injection of chlorphentermineM Adachi, C Tsai, M Greenbaum, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|December 1, 1970
Early evolution of cytoplasmic inclusion bodies in Tay-Sachs diseaseB W Volk, M Adachi, J Friedland, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|April 1, 1971
Screening for Tay-Sachs disease in utero using amniotic fluidJ Friedland, G Perle, A Saifer, et al.
American Journal of Obstetrics and Gynecology|February 15, 1973
Caveats of antenatal diagnosis of Tay-Sachs diseaseA Saifer, L Schneck, G Perle, et al.
Neurology|October 1, 1974
Fabry's disease in a black man without skin lesionsB W Volk, L Schneck, J E Clemmons, et al.
Journal of Neurochemistry|March 1, 1970
Cerebral lipids in a case of systemic Gm2-gangliosidosis of a late infantile typeC Klibansky, A Saifer, N I Feldman, et al.
Pediatrics|August 1, 1973
The Tay-Sachs disease fibroblast model: failure to respond to exogenous hexosaminidase AL Schneck, D Amsterdam, S E Brooks, et al.
Pageof 7