Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S S Raghavan

Showing results (21-30 of 44) with videos related to

Pageof 5
Sort By:
Journal of Neuropathology and Experimental Neurology|March 1, 1995
Mucolipidosis IV: morphology and histochemistry of an autopsy caseR D Folkerth, J Alroy, I Lomakina, et al.
Acta Neuropathologica|January 1, 1993
Adult-onset lysosomal storage disease in a Schipperke dog: clinical, morphological and biochemical studiesK Knowles, J Alroy, M Castagnaro, et al.
Placenta|September 1, 1987
Biochemical, ultrastructural and histochemical studies of cat placentae deficient in activity of lysosomal alpha-mannosidaseJ Alroy, C D Warren, S S Raghavan, et al.
Progress in Clinical and Biological Research|January 1, 1982
Phenotypic manifestations of Gaucher disease: clinical features in 48 biochemically verified type 1 patients and comment on type 2 patientsE H Kolodny, M D Ullman, H J Mankin, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|April 19, 2000
Randomized, controlled trial of caloric supplements in HIV infection. Terry Beirn Community Programs for Clinical Research on AIDSC L Gibert, D A Wheeler, G Collins, et al.
Pediatric Research|July 1, 1979
Abnormal copper metabolism in Menke's steely-hair syndromeI T Lott, R Dipaolo, S S Raghavan, et al.
Biochemical and Biophysical Research Communications|November 17, 1975
Deficiency of steroid beta-glucosidase in Gaucher diseaseJ N Kanfer, S S Raghavan, R A Mumford, et al.
The American Journal of Pathology|March 1, 1992
Canine GM1-gangliosidosis. A clinical, morphologic, histochemical, and biochemical comparison of two different modelsJ Alroy, U Orgad, R DeGasperi, et al.
Acta Neuropathologica|January 1, 1992
Adult onset lysosomal storage disease in a Tibetan terrier: clinical, morphological and biochemical studiesJ Alroy, S H Schelling, J G Thalhammer, et al.
Molecular Genetics and Metabolism|July 21, 2006
Rapid detection of three large novel deletions of the aspartoacylase gene in non-Jewish patients with Canavan diseaseB J Zeng, Z H Wang, P A Torres, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Journal of Neuropathology and Experimental Neurology|March 1, 1995
Mucolipidosis IV: morphology and histochemistry of an autopsy caseR D Folkerth, J Alroy, I Lomakina, et al.
Acta Neuropathologica|January 1, 1993
Adult-onset lysosomal storage disease in a Schipperke dog: clinical, morphological and biochemical studiesK Knowles, J Alroy, M Castagnaro, et al.
Placenta|September 1, 1987
Biochemical, ultrastructural and histochemical studies of cat placentae deficient in activity of lysosomal alpha-mannosidaseJ Alroy, C D Warren, S S Raghavan, et al.
Progress in Clinical and Biological Research|January 1, 1982
Phenotypic manifestations of Gaucher disease: clinical features in 48 biochemically verified type 1 patients and comment on type 2 patientsE H Kolodny, M D Ullman, H J Mankin, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|April 19, 2000
Randomized, controlled trial of caloric supplements in HIV infection. Terry Beirn Community Programs for Clinical Research on AIDSC L Gibert, D A Wheeler, G Collins, et al.
Pediatric Research|July 1, 1979
Abnormal copper metabolism in Menke's steely-hair syndromeI T Lott, R Dipaolo, S S Raghavan, et al.
Biochemical and Biophysical Research Communications|November 17, 1975
Deficiency of steroid beta-glucosidase in Gaucher diseaseJ N Kanfer, S S Raghavan, R A Mumford, et al.
The American Journal of Pathology|March 1, 1992
Canine GM1-gangliosidosis. A clinical, morphologic, histochemical, and biochemical comparison of two different modelsJ Alroy, U Orgad, R DeGasperi, et al.
Acta Neuropathologica|January 1, 1992
Adult onset lysosomal storage disease in a Tibetan terrier: clinical, morphological and biochemical studiesJ Alroy, S H Schelling, J G Thalhammer, et al.
Molecular Genetics and Metabolism|July 21, 2006
Rapid detection of three large novel deletions of the aspartoacylase gene in non-Jewish patients with Canavan diseaseB J Zeng, Z H Wang, P A Torres, et al.
Pageof 5