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

D M Danks

Showing results (211-220 of 255) with videos related to

Pageof 26
Sort By:
Biomedical Mass Spectrometry|July 1, 1979
The identification of 3-keto-2-methylvaleric acid and 3-hydroxy-2-methylvaleric acid in a patient with propionic acidemiaR J Truscott, C J Pullin, B Halpern, et al.
Biochimica Et Biophysica Acta|October 21, 1991
Developmental variation in copper, zinc and metallothionein mRNA in brindled mutant and nutritionally copper deficient miceJ F Mercer, T Stevenson, S A Wake, et al.
Biological Trace Element Research|November 1, 1989
The effect of tetrathiomolybdate on the metabolism of copper by hepatocytes and fibroblastsH J McArdle, S M Gross, H M Vogel, et al.
Prenatal Diagnosis|January 1, 1983
Prenatal determination of dihydropteridine reductase in a normal fetus at risk for malignant hyperphenylalaninemiaF A Firgaira, R G Cotton, D M Danks, et al.
Pediatric Nephrology (Berlin, Germany)|June 1, 1995
A case of craniomandibular dermatodysostosis associated with focal glomerulosclerosisE Pedagogos, G Flanagan, D M Francis, et al.
Australian Paediatric Journal|August 1, 1972
The Sanfilippo syndrome: clinical, biochemical, radiological, haematological and pathological features of nine casesD M Danks, P E Campbell, E Cartwright, et al.
Pediatric Research|October 1, 1979
Malignant hyperphenylalaninemia--clinical features, biochemical findings, and experience with administration of biopterinsD M Danks, P Schlesinger, F Firgaira, et al.
Lancet (London, England)|April 2, 1994
Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1D Ravine, R N Gibson, R G Walker, et al.
Lancet (London, England)|August 11, 1984
Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probeK H Choo, D George, G Filby, et al.
Pediatric Research|May 1, 1989
Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patientsS J Mihalik, H W Moser, P A Watkins, et al.
Pageof 26

Showing results (211-220 of 255) with videos related to

Sort By:
Pageof 26
Biomedical Mass Spectrometry|July 1, 1979
The identification of 3-keto-2-methylvaleric acid and 3-hydroxy-2-methylvaleric acid in a patient with propionic acidemiaR J Truscott, C J Pullin, B Halpern, et al.
Biochimica Et Biophysica Acta|October 21, 1991
Developmental variation in copper, zinc and metallothionein mRNA in brindled mutant and nutritionally copper deficient miceJ F Mercer, T Stevenson, S A Wake, et al.
Biological Trace Element Research|November 1, 1989
The effect of tetrathiomolybdate on the metabolism of copper by hepatocytes and fibroblastsH J McArdle, S M Gross, H M Vogel, et al.
Prenatal Diagnosis|January 1, 1983
Prenatal determination of dihydropteridine reductase in a normal fetus at risk for malignant hyperphenylalaninemiaF A Firgaira, R G Cotton, D M Danks, et al.
Pediatric Nephrology (Berlin, Germany)|June 1, 1995
A case of craniomandibular dermatodysostosis associated with focal glomerulosclerosisE Pedagogos, G Flanagan, D M Francis, et al.
Australian Paediatric Journal|August 1, 1972
The Sanfilippo syndrome: clinical, biochemical, radiological, haematological and pathological features of nine casesD M Danks, P E Campbell, E Cartwright, et al.
Pediatric Research|October 1, 1979
Malignant hyperphenylalaninemia--clinical features, biochemical findings, and experience with administration of biopterinsD M Danks, P Schlesinger, F Firgaira, et al.
Lancet (London, England)|April 2, 1994
Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1D Ravine, R N Gibson, R G Walker, et al.
Lancet (London, England)|August 11, 1984
Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probeK H Choo, D George, G Filby, et al.
Pediatric Research|May 1, 1989
Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patientsS J Mihalik, H W Moser, P A Watkins, et al.
Pageof 26