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

M A Skomorowski

Showing results (1-10 of 17) with videos related to

Pageof 2
Sort By:
American Journal of Medical Genetics|May 1, 1989
Marked clinical difference between two sibs affected with juvenile metachromatic leukodystrophyJ T Clarke, M A Skomorowski, P L Chang
American Journal of Medical Genetics|December 1, 1989
Tay-Sachs disease carrier screening: follow-up of a case-finding approachJ T Clarke, M A Skomorowski, S Zuker
Journal of Lipid Research|January 1, 1989
Simultaneous fractionation of four placental neutral glycosphingolipids with a continuous gradientP Strasberg, A Grey, I Warren, et al.
Canadian Medical Association Journal|August 3, 1974
Screening for carriers of Tay-Sachs disease: A community projectJ A Lowden, S Zuker, A J Wilensky, et al.
Clinical Biochemistry|April 1, 1985
HPLC analysis of urinary sulfatide: an aid in the diagnosis of metachromatic leukodystrophyP M Strasberg, I Warren, M A Skomorowski, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 31, 1983
HPLC analysis of neutral glycolipids: an aid in the diagnosis of lysosomal storage diseaseP M Strasberg, I Warren, M A Skomorowski, et al.
Clinical Biochemistry|December 1, 1990
First trimester prenatal diagnosis of Tay-Sachs disease using the sulfated synthetic substrate for hexosaminidase AJ W Callahan, A Archibald, M A Skomorowski, et al.
Clinical Genetics|May 1, 1990
Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girlJ T Clarke, H F Willard, I Teshima, et al.
Journal of Child Neurology|July 1, 1991
Multiple sulfatase deficiency with early severe retinal degenerationM Harbord, J R Buncic, S A Chuang, et al.
Neurology|June 1, 1981
Type 2 GM1 gangliosidosis with long survival and neuronal ceroid lipofuscinosisJ A Lowden, J W Callahan, R A Gravel, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|May 1, 1989
Marked clinical difference between two sibs affected with juvenile metachromatic leukodystrophyJ T Clarke, M A Skomorowski, P L Chang
American Journal of Medical Genetics|December 1, 1989
Tay-Sachs disease carrier screening: follow-up of a case-finding approachJ T Clarke, M A Skomorowski, S Zuker
Journal of Lipid Research|January 1, 1989
Simultaneous fractionation of four placental neutral glycosphingolipids with a continuous gradientP Strasberg, A Grey, I Warren, et al.
Canadian Medical Association Journal|August 3, 1974
Screening for carriers of Tay-Sachs disease: A community projectJ A Lowden, S Zuker, A J Wilensky, et al.
Clinical Biochemistry|April 1, 1985
HPLC analysis of urinary sulfatide: an aid in the diagnosis of metachromatic leukodystrophyP M Strasberg, I Warren, M A Skomorowski, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 31, 1983
HPLC analysis of neutral glycolipids: an aid in the diagnosis of lysosomal storage diseaseP M Strasberg, I Warren, M A Skomorowski, et al.
Clinical Biochemistry|December 1, 1990
First trimester prenatal diagnosis of Tay-Sachs disease using the sulfated synthetic substrate for hexosaminidase AJ W Callahan, A Archibald, M A Skomorowski, et al.
Clinical Genetics|May 1, 1990
Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girlJ T Clarke, H F Willard, I Teshima, et al.
Journal of Child Neurology|July 1, 1991
Multiple sulfatase deficiency with early severe retinal degenerationM Harbord, J R Buncic, S A Chuang, et al.
Neurology|June 1, 1981
Type 2 GM1 gangliosidosis with long survival and neuronal ceroid lipofuscinosisJ A Lowden, J W Callahan, R A Gravel, et al.
Pageof 2