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American Journal of Medical Genetics
|
June 5, 1995
Canine hereditary ceroid-lipofuscinosis: evidence for a defect in the carnitine biosynthetic pathway
M L Katz, A N Siakotos
American Journal of Medical Genetics
|
June 5, 1995
Early detection of canine ceroid-lipofuscinosis (CCL): an ultrastructural study
J Savill, B Azzarelli, A N Siakotos
American Journal of Medical Genetics
|
February 15, 1992
Perspective of biochemical research in the neuronal ceroid-lipofuscinosis
J A Rider, G Dawson, A N Siakotos
Advances in Experimental Medicine and Biology
|
January 1, 1989
Phospholipases and the molecular basis for the formation of ceroid in Batten disease
G Dawson, S A Dawson, A N Siakotos
Molecular and Chemical Neuropathology
|
October 1, 1996
Mitochondrial abnormalities in CLN2 and CLN3 forms of Batten disease
G Dawson, J Kilkus, A N Siakotos, et al.
American Journal of Medical Genetics
|
February 15, 1992
Evidence for lipase abnormality: high levels of free and triacylglycerol forms of unsaturated fatty acids in neuronal ceroid-lipofuscinosis tissue
P Banerjee, A Dasgupta, A N Siakotos, et al.
Neuropediatrics
|
February 1, 1997
Low molecular weight storage material in infantile ceroid lipofuscinosis (CLN1)
G Dawson, S Cho, A N Siakotos, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 1978
Studies on the retina and the pigment epithelium in hereditary canine ceroid lipofuscinosis. II. The subcellular distribution of lysosomal hydrolases and other enzymes
A N Siakotos, D Armstrong, N Koppang, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1988
Characterization of disease-specific brain fluorophores in ceroid-lipofuscinosis
M L Katz, G E Eldred, A N Siakotos, et al.
Neurochemical Research
|
August 5, 1998
Altered mitochondrial function in canine ceroid-lipofuscinosis
A N Siakotos, P S Blair, J D Savill, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics
|
June 5, 1995
Canine hereditary ceroid-lipofuscinosis: evidence for a defect in the carnitine biosynthetic pathway
M L Katz, A N Siakotos
American Journal of Medical Genetics
|
June 5, 1995
Early detection of canine ceroid-lipofuscinosis (CCL): an ultrastructural study
J Savill, B Azzarelli, A N Siakotos
American Journal of Medical Genetics
|
February 15, 1992
Perspective of biochemical research in the neuronal ceroid-lipofuscinosis
J A Rider, G Dawson, A N Siakotos
Advances in Experimental Medicine and Biology
|
January 1, 1989
Phospholipases and the molecular basis for the formation of ceroid in Batten disease
G Dawson, S A Dawson, A N Siakotos
Molecular and Chemical Neuropathology
|
October 1, 1996
Mitochondrial abnormalities in CLN2 and CLN3 forms of Batten disease
G Dawson, J Kilkus, A N Siakotos, et al.
American Journal of Medical Genetics
|
February 15, 1992
Evidence for lipase abnormality: high levels of free and triacylglycerol forms of unsaturated fatty acids in neuronal ceroid-lipofuscinosis tissue
P Banerjee, A Dasgupta, A N Siakotos, et al.
Neuropediatrics
|
February 1, 1997
Low molecular weight storage material in infantile ceroid lipofuscinosis (CLN1)
G Dawson, S Cho, A N Siakotos, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 1978
Studies on the retina and the pigment epithelium in hereditary canine ceroid lipofuscinosis. II. The subcellular distribution of lysosomal hydrolases and other enzymes
A N Siakotos, D Armstrong, N Koppang, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1988
Characterization of disease-specific brain fluorophores in ceroid-lipofuscinosis
M L Katz, G E Eldred, A N Siakotos, et al.
Neurochemical Research
|
August 5, 1998
Altered mitochondrial function in canine ceroid-lipofuscinosis
A N Siakotos, P S Blair, J D Savill, et al.
Page
of 3