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

R R Howell

Showing results (41-50 of 67) with videos related to

Pageof 7
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1976
Menkes disease: a biochemical abnormality in cultured human fibroblastsT J Goka, R E Stevenson, P M Hefferan, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 1, 1988
Hypertension in a child with type IA glycogen storage diseaseA J Jonas, R R Verani, R R Howell, et al.
Lancet (London, England)|March 18, 1978
Pili torti as marker for carriers of Menkes diseaseW R Collie, C M Moore, T J Goka, et al.
Developmental Biology|September 1, 1976
Development of gluconeogenic enzymes in fetal sheep liver and kidneyR E Stevenson, F H Morriss, E W Adcock, et al.
The Journal of Pediatrics|May 1, 1981
Neurotransmitter defects and treatment of disorders of hyperphenylalaninemiaI J Butler, M E O'Flynn, W E Seifert, et al.
The Journal of Laboratory and Clinical Medicine|July 1, 1983
X-ray fluorescence spectrometry in the analysis of trace elements in human milkP A Palma, W E Seifert, R M Caprioli, et al.
American Journal of Obstetrics and Gynecology|September 1, 1971
Developmental changes in amino acid concentrations in human amniotic fluid: abnormal findings in maternal phenylketonuriaG H Thomas, T H Parmley, R E Stevenson, et al.
American Journal of Ophthalmology|September 1, 1976
Ocular findings in mannosidosisA I Arbisser, A L Murphree, C A Garcia, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1971
GM1-gangliosidosis. Ocular and pathological manifestationsJ M Emery, W R Green, R G Wyllie, et al.
The American Journal of Medicine|July 1, 1979
Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiencyB M Patten, J M Wood, Y Harati, et al.
Pageof 7

Showing results (41-50 of 67) with videos related to

Sort By:
Pageof 7
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1976
Menkes disease: a biochemical abnormality in cultured human fibroblastsT J Goka, R E Stevenson, P M Hefferan, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 1, 1988
Hypertension in a child with type IA glycogen storage diseaseA J Jonas, R R Verani, R R Howell, et al.
Lancet (London, England)|March 18, 1978
Pili torti as marker for carriers of Menkes diseaseW R Collie, C M Moore, T J Goka, et al.
Developmental Biology|September 1, 1976
Development of gluconeogenic enzymes in fetal sheep liver and kidneyR E Stevenson, F H Morriss, E W Adcock, et al.
The Journal of Pediatrics|May 1, 1981
Neurotransmitter defects and treatment of disorders of hyperphenylalaninemiaI J Butler, M E O'Flynn, W E Seifert, et al.
The Journal of Laboratory and Clinical Medicine|July 1, 1983
X-ray fluorescence spectrometry in the analysis of trace elements in human milkP A Palma, W E Seifert, R M Caprioli, et al.
American Journal of Obstetrics and Gynecology|September 1, 1971
Developmental changes in amino acid concentrations in human amniotic fluid: abnormal findings in maternal phenylketonuriaG H Thomas, T H Parmley, R E Stevenson, et al.
American Journal of Ophthalmology|September 1, 1976
Ocular findings in mannosidosisA I Arbisser, A L Murphree, C A Garcia, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1971
GM1-gangliosidosis. Ocular and pathological manifestationsJ M Emery, W R Green, R G Wyllie, et al.
The American Journal of Medicine|July 1, 1979
Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiencyB M Patten, J M Wood, Y Harati, et al.
Pageof 7