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

J W McReynolds

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
Neurology|April 1, 1984
Valproic acid-induced hyperammonemia in mentally retarded adultsC A Williams, S Tiefenbach, J W McReynolds
The Journal of Pediatrics|September 1, 1978
Treatment of complete ornithine transcarbamylase deficiency with nitrogen-free analogues of essential amino acidsJ W McReynolds, S Mantagos, S Brusilow, et al.
Journal of Medical Genetics|October 1, 1981
Complete trisomy 9 in two liveborn infantsS Mantagos, J W McReynolds, M R Seashore, et al.
American Journal of Human Genetics|May 1, 1981
Autosomal recessive inheritance of human mitochondrial carbamyl phosphate synthetase deficiencyJ W McReynolds, B Crowley, M J Mahoney, et al.
Hepatology (Baltimore, Md.)|May 1, 1984
Liver ultrastructure in mitochondrial urea cycle enzyme deficiencies and comparison with Reye's syndromeP S Latham, D R LaBrecque, J W McReynolds, et al.
Lancet (London, England)|February 23, 1974
Letter: Ampicillin-resistant Haemophilus influenzae meningitisW J Thomas, J W McReynolds, C R Mock, et al.
Lancet (London, England)|August 3, 1974
Clinical, bacteriological, and immunological characterisation of ampicillin-resistant Haemophilus influenzae type BM S Schiffer, J MacLowry, R Schneerson, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Neurology|April 1, 1984
Valproic acid-induced hyperammonemia in mentally retarded adultsC A Williams, S Tiefenbach, J W McReynolds
The Journal of Pediatrics|September 1, 1978
Treatment of complete ornithine transcarbamylase deficiency with nitrogen-free analogues of essential amino acidsJ W McReynolds, S Mantagos, S Brusilow, et al.
Journal of Medical Genetics|October 1, 1981
Complete trisomy 9 in two liveborn infantsS Mantagos, J W McReynolds, M R Seashore, et al.
American Journal of Human Genetics|May 1, 1981
Autosomal recessive inheritance of human mitochondrial carbamyl phosphate synthetase deficiencyJ W McReynolds, B Crowley, M J Mahoney, et al.
Hepatology (Baltimore, Md.)|May 1, 1984
Liver ultrastructure in mitochondrial urea cycle enzyme deficiencies and comparison with Reye's syndromeP S Latham, D R LaBrecque, J W McReynolds, et al.
Lancet (London, England)|February 23, 1974
Letter: Ampicillin-resistant Haemophilus influenzae meningitisW J Thomas, J W McReynolds, C R Mock, et al.
Lancet (London, England)|August 3, 1974
Clinical, bacteriological, and immunological characterisation of ampicillin-resistant Haemophilus influenzae type BM S Schiffer, J MacLowry, R Schneerson, et al.
Pageof 1