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A B Moser

Showing results (41-50 of 86) with videos related to

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The New England Journal of Medicine|February 12, 1987
Myelin basic protein as an encephalitogen in encephalomyelitis and polyneuritis following rabies vaccinationT Hemachudha, D E Griffin, J J Giffels, et al.
Prenatal Diagnosis|October 1, 1988
Prenatal diagnosis of rhizomelic chondrodysplasia punctataS Hoefler, G Hoefler, A B Moser, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1981
Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cellsB R Migeon, H W Moser, A B Moser, et al.
Annals of Neurology|December 1, 1985
Identification of the inflammatory cells in the central nervous system of patients with adrenoleukodystrophyD E Griffin, H W Moser, Q Mendoza, et al.
Annals of Neurology|March 1, 1987
A new dietary therapy for adrenoleukodystrophy: biochemical and preliminary clinical results in 36 patientsA B Moser, J Borel, A Odone, et al.
The Johns Hopkins Medical Journal|December 1, 1980
Adrenoleukodystrophy: studies of the phenotype, genetics and biochemistryH W Moser, A B Moser, N Kawamura, et al.
Annals of Neurology|January 23, 1999
Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controlsA B Moser, N Kreiter, L Bezman, 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 secretionR Périchon, A B Moser, W C Wallace, et al.
Prenatal Diagnosis|May 18, 1999
Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiencyK 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 deficiencyM R Natowicz, J E Evans, R I Kelley, et al.
Pageof 9

Showing results (41-50 of 86) with videos related to

Sort By:
Pageof 9
The New England Journal of Medicine|February 12, 1987
Myelin basic protein as an encephalitogen in encephalomyelitis and polyneuritis following rabies vaccinationT Hemachudha, D E Griffin, J J Giffels, et al.
Prenatal Diagnosis|October 1, 1988
Prenatal diagnosis of rhizomelic chondrodysplasia punctataS Hoefler, G Hoefler, A B Moser, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1981
Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cellsB R Migeon, H W Moser, A B Moser, et al.
Annals of Neurology|December 1, 1985
Identification of the inflammatory cells in the central nervous system of patients with adrenoleukodystrophyD E Griffin, H W Moser, Q Mendoza, et al.
Annals of Neurology|March 1, 1987
A new dietary therapy for adrenoleukodystrophy: biochemical and preliminary clinical results in 36 patientsA B Moser, J Borel, A Odone, et al.
The Johns Hopkins Medical Journal|December 1, 1980
Adrenoleukodystrophy: studies of the phenotype, genetics and biochemistryH W Moser, A B Moser, N Kawamura, et al.
Annals of Neurology|January 23, 1999
Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controlsA B Moser, N Kreiter, L Bezman, 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 secretionR Périchon, A B Moser, W C Wallace, et al.
Prenatal Diagnosis|May 18, 1999
Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiencyK 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 deficiencyM R Natowicz, J E Evans, R I Kelley, et al.
Pageof 9