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A D Patrick

Showing results (41-50 of 53) with videos related to

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Advances in Experimental Medicine and Biology|January 1, 1989
Glycoconjugates in storage cytosomes from ceroid-lipofuscinosis (Batten's disease) and in lipofuscin from old-age brainN A Hall, B D Lake, D N Palmer, et al.
Biochimica Et Biophysica Acta|December 8, 1989
Analysis of dolichyl pyrophosphoryl oligosaccharides in purified storage cytosomes from ovine ceroid-lipofuscinosisN A Hall, R D Jolly, D N Palmer, et al.
British Journal of Haematology|April 1, 1987
Grey platelet syndrome: studies on platelet alpha-granules, lysosomes and defective response to thrombinP C Srivastava, M J Powling, T J Nokes, et al.
Biochemical and Biophysical Research Communications|July 8, 1975
Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidaseJ D Schulman, S I Goodman, J W Mace, et al.
American Journal of Medical Genetics|February 15, 1992
Stored dolichyl pyrophosphoryl oligosaccharides in Batten diseaseN A Hall, J E Thomas-Oates, A Dell, et al.
Journal of Submicroscopic Cytology|October 1, 1981
Axo-dendritic abnormalities in a case of juvenile neuronal storage diseaseM M Paula-Barbosa, M A Tavares, C A Silva, et al.
Brain : a Journal of Neurology|December 1, 1985
Acid maltase deficiency in adults. Diagnosis and management in five casesP S Trend, C M Wiles, G T Spencer, et al.
Archives of Disease in Childhood|October 1, 1973
Late onset GM2-gangliosidosis. Clinical, pathological, and biochemical studies on 8 patientsE M Brett, R B Ellis, L Haas, et al.
Prenatal Diagnosis|April 1, 1981
Correct prenatal diagnosis of a Hurler fetus where amniotic fluid cell cultures were of maternal originJ Mossman, A D Patrick, A H Fensom, et al.
Prenatal Diagnosis|October 1, 1983
Prenatal tests for Sanfilippo disease type B in four pregnanciesJ Mossman, E P Young, A D Patrick, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Advances in Experimental Medicine and Biology|January 1, 1989
Glycoconjugates in storage cytosomes from ceroid-lipofuscinosis (Batten's disease) and in lipofuscin from old-age brainN A Hall, B D Lake, D N Palmer, et al.
Biochimica Et Biophysica Acta|December 8, 1989
Analysis of dolichyl pyrophosphoryl oligosaccharides in purified storage cytosomes from ovine ceroid-lipofuscinosisN A Hall, R D Jolly, D N Palmer, et al.
British Journal of Haematology|April 1, 1987
Grey platelet syndrome: studies on platelet alpha-granules, lysosomes and defective response to thrombinP C Srivastava, M J Powling, T J Nokes, et al.
Biochemical and Biophysical Research Communications|July 8, 1975
Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidaseJ D Schulman, S I Goodman, J W Mace, et al.
American Journal of Medical Genetics|February 15, 1992
Stored dolichyl pyrophosphoryl oligosaccharides in Batten diseaseN A Hall, J E Thomas-Oates, A Dell, et al.
Journal of Submicroscopic Cytology|October 1, 1981
Axo-dendritic abnormalities in a case of juvenile neuronal storage diseaseM M Paula-Barbosa, M A Tavares, C A Silva, et al.
Brain : a Journal of Neurology|December 1, 1985
Acid maltase deficiency in adults. Diagnosis and management in five casesP S Trend, C M Wiles, G T Spencer, et al.
Archives of Disease in Childhood|October 1, 1973
Late onset GM2-gangliosidosis. Clinical, pathological, and biochemical studies on 8 patientsE M Brett, R B Ellis, L Haas, et al.
Prenatal Diagnosis|April 1, 1981
Correct prenatal diagnosis of a Hurler fetus where amniotic fluid cell cultures were of maternal originJ Mossman, A D Patrick, A H Fensom, et al.
Prenatal Diagnosis|October 1, 1983
Prenatal tests for Sanfilippo disease type B in four pregnanciesJ Mossman, E P Young, A D Patrick, et al.
Pageof 6