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W Moser

Showing results (361-370 of 466) with videos related to

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Journal of Lipid Research|December 20, 1999
Ether lipid biosynthesis: alkyl-dihydroxyacetonephosphate synthase protein deficiency leads to reduced dihydroxyacetonephosphate acyltransferase activitiesE C de Vet, L Ijlst, W Oostheim, et al.
Journal of Molecular Neuroscience : MN|August 2, 2001
Brain uptake and utilization of fatty acids: recommendations for future researchR Katz, J A Hamilton, A A Spector, et al.
Neuropediatrics|February 24, 2001
X-Linked adrenoleukodystrophy: overview and prognosis as a function of age and brain magnetic resonance imaging abnormality. A study involving 372 patientsH W Moser, D J Loes, E R Melhem, et al.
Biochemical and Biophysical Research Communications|May 15, 1978
High concentration of hexacosanoate in cultured skin fibroblast lipids from adrenoleukodystrophy patientsN Kawamura, A B Moser, H W Moser, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Phytanoyl-CoA hydroxylase is not only deficient in classical Refsum disease but also in rhizomelic chondrodysplasia punctataG A Jansen, S J Mihalik, P A Watkins, et al.
The New England Journal of Medicine|February 14, 1985
Prenatal diagnosis of Zellweger cerebrohepatorenal syndromeA K Hajra, N S Datta, L G Jackson, et al.
Pediatric Neurology|June 1, 1994
CSF findings in adrenoleukodystrophy: correlation between measures of cytokines, IgG production, and disease severityJ P Phillips, L A Lockman, E G Shapiro, et al.
Biochimica Et Biophysica Acta|August 8, 1989
Properties of acid ceramidase from human spleenB J Al, C W Tiffany, D S Gomes de Mesquita, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1985
Niemann-Pick disease--type C. Ocular histopathologic and electron microscopic studiesM Palmer, W R Green, I H Maumenee, et al.
Birth Defects Original Article Series|January 1, 1986
Allogeneic bone marrow transplantation in adrenoleukodystrophy: clinical, pathologic, and biochemical studiesA M Yeager, H W Moser, P J Tutschka, et al.
Pageof 47

Showing results (361-370 of 466) with videos related to

Sort By:
Pageof 47
Journal of Lipid Research|December 20, 1999
Ether lipid biosynthesis: alkyl-dihydroxyacetonephosphate synthase protein deficiency leads to reduced dihydroxyacetonephosphate acyltransferase activitiesE C de Vet, L Ijlst, W Oostheim, et al.
Journal of Molecular Neuroscience : MN|August 2, 2001
Brain uptake and utilization of fatty acids: recommendations for future researchR Katz, J A Hamilton, A A Spector, et al.
Neuropediatrics|February 24, 2001
X-Linked adrenoleukodystrophy: overview and prognosis as a function of age and brain magnetic resonance imaging abnormality. A study involving 372 patientsH W Moser, D J Loes, E R Melhem, et al.
Biochemical and Biophysical Research Communications|May 15, 1978
High concentration of hexacosanoate in cultured skin fibroblast lipids from adrenoleukodystrophy patientsN Kawamura, A B Moser, H W Moser, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Phytanoyl-CoA hydroxylase is not only deficient in classical Refsum disease but also in rhizomelic chondrodysplasia punctataG A Jansen, S J Mihalik, P A Watkins, et al.
The New England Journal of Medicine|February 14, 1985
Prenatal diagnosis of Zellweger cerebrohepatorenal syndromeA K Hajra, N S Datta, L G Jackson, et al.
Pediatric Neurology|June 1, 1994
CSF findings in adrenoleukodystrophy: correlation between measures of cytokines, IgG production, and disease severityJ P Phillips, L A Lockman, E G Shapiro, et al.
Biochimica Et Biophysica Acta|August 8, 1989
Properties of acid ceramidase from human spleenB J Al, C W Tiffany, D S Gomes de Mesquita, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1985
Niemann-Pick disease--type C. Ocular histopathologic and electron microscopic studiesM Palmer, W R Green, I H Maumenee, et al.
Birth Defects Original Article Series|January 1, 1986
Allogeneic bone marrow transplantation in adrenoleukodystrophy: clinical, pathologic, and biochemical studiesA M Yeager, H W Moser, P J Tutschka, et al.
Pageof 47