Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

W Moser

Showing results (301-310 of 466) with videos related to

Pageof 47
Sort By:
Archives of Neurology|May 16, 2007
Magnetic resonance imaging detection of lesion progression in adult patients with X-linked adrenoleukodystrophyFlorian Eichler, Asif Mahmood, Daniel Loes, et al.
Prenatal Diagnosis|January 1, 1985
The prenatal diagnosis of the cerebro-hepato-renal syndrome of ZellwegerG I Solish, H W Moser, L D Ringer, et al.
Prenatal Diagnosis|October 1, 1988
Prenatal diagnosis of rhizomelic chondrodysplasia punctataS Hoefler, G Hoefler, A B Moser, et al.
American Journal of Medical Genetics|April 1, 1987
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophyR Cotrufo, M A Melone, M R Monsurro, et al.
Deutsche Medizinische Wochenschrift (1946)|October 3, 1986
[Adrenomyeloneuropathy, a rare cause of primary adrenal cortex insufficiency]K Frank, O Schrecker, K Brosi, 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.
The Archives of Bone and Joint Surgery|November 10, 2015
Failure of Anterior Cruciate Ligament ReconstructionGonzalo Samitier, Alejandro I Marcano, Eduard Alentorn-Geli, et al.
Archives of Neurology|January 13, 2006
Sensorimotor function and axonal integrity in adrenomyeloneuropathyKathleen M Zackowski, Prachi Dubey, Gerald V Raymond, et al.
The Journal of Pediatrics|March 1, 1984
Phenotypic variability in siblings with Farber diseaseS E Antonarakis, D Valle, H W Moser, et al.
Pageof 47

Showing results (301-310 of 466) with videos related to

Sort By:
Pageof 47
Archives of Neurology|May 16, 2007
Magnetic resonance imaging detection of lesion progression in adult patients with X-linked adrenoleukodystrophyFlorian Eichler, Asif Mahmood, Daniel Loes, et al.
Prenatal Diagnosis|January 1, 1985
The prenatal diagnosis of the cerebro-hepato-renal syndrome of ZellwegerG I Solish, H W Moser, L D Ringer, et al.
Prenatal Diagnosis|October 1, 1988
Prenatal diagnosis of rhizomelic chondrodysplasia punctataS Hoefler, G Hoefler, A B Moser, et al.
American Journal of Medical Genetics|April 1, 1987
Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophyR Cotrufo, M A Melone, M R Monsurro, et al.
Deutsche Medizinische Wochenschrift (1946)|October 3, 1986
[Adrenomyeloneuropathy, a rare cause of primary adrenal cortex insufficiency]K Frank, O Schrecker, K Brosi, 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.
The Archives of Bone and Joint Surgery|November 10, 2015
Failure of Anterior Cruciate Ligament ReconstructionGonzalo Samitier, Alejandro I Marcano, Eduard Alentorn-Geli, et al.
Archives of Neurology|January 13, 2006
Sensorimotor function and axonal integrity in adrenomyeloneuropathyKathleen M Zackowski, Prachi Dubey, Gerald V Raymond, et al.
The Journal of Pediatrics|March 1, 1984
Phenotypic variability in siblings with Farber diseaseS E Antonarakis, D Valle, H W Moser, et al.
Pageof 47