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American Journal of Ophthalmology
|
March 1, 1983
Ocular clinicopathologic correlation of Hallervorden-Spatz syndrome with acanthocytosis and pigmentary retinopathy
M W Luckenbach, W R Green, N R Miller, et al.
Annals of Neurology
|
January 23, 1999
Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls
A B Moser, N Kreiter, L Bezman, et al.
The American Journal of Clinical Nutrition
|
August 1, 1984
The design of a diet restricted in saturated very long-chain fatty acids: therapeutic application in adrenoleukodystrophy
M A Van Duyn, A E Moser, F R Brown, et al.
Magnetic Resonance Imaging
|
March 21, 2000
Visualization of Taylor-Couette and spiral Poiseuille flows using a snapshot FLASH spatial tagging sequence
K W Moser, L G Raguin, A Harris, et al.
Journal of Child Neurology
|
January 1, 1988
Research on Rett syndrome: strategy and preliminary results
S Naidu, C A Kitt, D F Wong, et al.
Biochemical and Biophysical Research Communications
|
July 24, 1998
Peroxisomal disease cell lines with cellular plasmalogen deficiency have impaired muscarinic cholinergic signal transduction activity and amyloid precursor protein secretion
R Périchon, A B Moser, W C Wallace, et al.
Transactions of the American Neurological Association
|
January 1, 1978
Successful immunocytochemical localization of myelin components in paraffin sections of human nervous tissue with preliminary observations on multiple sclerosis and metachromatic leukodystrophy lesions
Y Itoyama, N Sternberger, R Quarles, et al.
Prenatal Diagnosis
|
May 18, 1999
Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiency
K M Brookhyser, M H Lipson, A B Moser, et al.
American Journal of Medical Genetics
|
May 17, 1996
Urinary bile acids and peroxisomal bifunctional enzyme deficiency
M R Natowicz, J E Evans, R I Kelley, et al.
Acta Neuropathologica
|
January 1, 1987
Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndrome
J M Powers, R C Tummons, A B Moser, et al.
Page
of 47
Search research articles
Search
Showing results (321-330 of 466) with videos related to
Sort By:
Page
of 47
American Journal of Ophthalmology
|
March 1, 1983
Ocular clinicopathologic correlation of Hallervorden-Spatz syndrome with acanthocytosis and pigmentary retinopathy
M W Luckenbach, W R Green, N R Miller, et al.
Annals of Neurology
|
January 23, 1999
Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls
A B Moser, N Kreiter, L Bezman, et al.
The American Journal of Clinical Nutrition
|
August 1, 1984
The design of a diet restricted in saturated very long-chain fatty acids: therapeutic application in adrenoleukodystrophy
M A Van Duyn, A E Moser, F R Brown, et al.
Magnetic Resonance Imaging
|
March 21, 2000
Visualization of Taylor-Couette and spiral Poiseuille flows using a snapshot FLASH spatial tagging sequence
K W Moser, L G Raguin, A Harris, et al.
Journal of Child Neurology
|
January 1, 1988
Research on Rett syndrome: strategy and preliminary results
S Naidu, C A Kitt, D F Wong, et al.
Biochemical and Biophysical Research Communications
|
July 24, 1998
Peroxisomal disease cell lines with cellular plasmalogen deficiency have impaired muscarinic cholinergic signal transduction activity and amyloid precursor protein secretion
R Périchon, A B Moser, W C Wallace, et al.
Transactions of the American Neurological Association
|
January 1, 1978
Successful immunocytochemical localization of myelin components in paraffin sections of human nervous tissue with preliminary observations on multiple sclerosis and metachromatic leukodystrophy lesions
Y Itoyama, N Sternberger, R Quarles, et al.
Prenatal Diagnosis
|
May 18, 1999
Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiency
K M Brookhyser, M H Lipson, A B Moser, et al.
American Journal of Medical Genetics
|
May 17, 1996
Urinary bile acids and peroxisomal bifunctional enzyme deficiency
M R Natowicz, J E Evans, R I Kelley, et al.
Acta Neuropathologica
|
January 1, 1987
Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndrome
J M Powers, R C Tummons, A B Moser, et al.
Page
of 47