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

N A Carson

Showing results (1-10 of 20) with videos related to

Pageof 2
Sort By:
Archives of Disease in Childhood|December 1, 1971
Diagnosis and management of hyperphenylalaninaemiaN A Carson
Clinics in Endocrinology and Metabolism|March 1, 1974
Metabolic errors in lysine degradationN A Carson
Proceedings of the Royal Society of Medicine|January 1, 1970
HomocystinuriaN A Carson
Archives of Disease in Childhood|December 1, 1971
Management of hyperphenylalaninaemia (HPA) in Northern IrelandN A Carson
Annals of Clinical Biochemistry|May 1, 1977
Lysinuric protein intoleranceN A Carson, O A Redmond
Journal of Medical Genetics|June 1, 1974
Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuriaA H Bittles, N A Carson
The Journal of Obstetrics and Gynaecology of the British Commonwealth|July 1, 1973
Pregnancy and homocystinuriaJ W Ritchie, N A Carson
Journal of Inherited Metabolic Disease|January 1, 1981
Homocystinuria: studies on cystathionine beta-synthase, S-adenosylmethionine synthetase and cystathionase activities in skin fibroblastsA H Bittles, N A Carson
Journal of Inherited Metabolic Disease|January 1, 1981
Homocystinuria: the effect of pyridoxine supplementation on cultured skin fibroblastsA H Bittles, N A Carson
Journal of Medical Genetics|June 1, 1973
Tissue culture techniques as an aid to prenatal diagnosis and genetic counselling in homocystinuriaA H Bittles, N A Carson
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Archives of Disease in Childhood|December 1, 1971
Diagnosis and management of hyperphenylalaninaemiaN A Carson
Clinics in Endocrinology and Metabolism|March 1, 1974
Metabolic errors in lysine degradationN A Carson
Proceedings of the Royal Society of Medicine|January 1, 1970
HomocystinuriaN A Carson
Archives of Disease in Childhood|December 1, 1971
Management of hyperphenylalaninaemia (HPA) in Northern IrelandN A Carson
Annals of Clinical Biochemistry|May 1, 1977
Lysinuric protein intoleranceN A Carson, O A Redmond
Journal of Medical Genetics|June 1, 1974
Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuriaA H Bittles, N A Carson
The Journal of Obstetrics and Gynaecology of the British Commonwealth|July 1, 1973
Pregnancy and homocystinuriaJ W Ritchie, N A Carson
Journal of Inherited Metabolic Disease|January 1, 1981
Homocystinuria: studies on cystathionine beta-synthase, S-adenosylmethionine synthetase and cystathionase activities in skin fibroblastsA H Bittles, N A Carson
Journal of Inherited Metabolic Disease|January 1, 1981
Homocystinuria: the effect of pyridoxine supplementation on cultured skin fibroblastsA H Bittles, N A Carson
Journal of Medical Genetics|June 1, 1973
Tissue culture techniques as an aid to prenatal diagnosis and genetic counselling in homocystinuriaA H Bittles, N A Carson
Pageof 2