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 J Pollitt

Showing results (21-30 of 133) with videos related to

Pageof 14
Sort By:
Archives of Disease in Childhood|January 1, 1987
Inherited disorders of straight chain fatty acid oxidationR J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1979
The occurrence of gamma-glutamylphenylalanine in the urine of newborn phenylketonuricsH Peck, R J Pollitt
Journal of Inherited Metabolic Disease|July 17, 1999
Population newborn screening for inherited metabolic disease: current UK perspectivesA Green, R J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1978
3-Aminopiperid-2-one, an unusual metabolite in the urine of a patient with hyperammonaemia, hyperornithinaemia and homocitrullinuriaV Fell, R J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1980
Ascorbic acid: an unstable ninhydrin-positive urinary constituent running with valine in a commonly used screening systemR J Pollitt, B Sandhu
The Journal of Pharmacy and Pharmacology|May 1, 1976
The hydroxylation of p-tyramine in manR A Jones, R J Pollitt
The Biochemical Journal|July 1, 1972
Glycoasparagines in the urine of patients with aspartylglycosaminuriaR J Pollitt, K M Pretty
Journal of Chromatography|March 1, 1978
The determination of 5-methoxyindole-3-acetic acid in human urine by mass fragmentographyJ A Hoskins, R J Pollitt
Archives Francaises De Pediatrie|January 1, 1987
[Attitude of parents toward the prenatal diagnosis of phenylketonuria]B E Barwell, R J Pollitt
The Biochemical Journal|January 1, 1972
New derivatives of argininosuccinic acid in the urine of a patient with argininosuccinicaciduriaC R Lee, R J Pollitt
Pageof 14

Showing results (21-30 of 133) with videos related to

Sort By:
Pageof 14
Archives of Disease in Childhood|January 1, 1987
Inherited disorders of straight chain fatty acid oxidationR J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1979
The occurrence of gamma-glutamylphenylalanine in the urine of newborn phenylketonuricsH Peck, R J Pollitt
Journal of Inherited Metabolic Disease|July 17, 1999
Population newborn screening for inherited metabolic disease: current UK perspectivesA Green, R J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1978
3-Aminopiperid-2-one, an unusual metabolite in the urine of a patient with hyperammonaemia, hyperornithinaemia and homocitrullinuriaV Fell, R J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1980
Ascorbic acid: an unstable ninhydrin-positive urinary constituent running with valine in a commonly used screening systemR J Pollitt, B Sandhu
The Journal of Pharmacy and Pharmacology|May 1, 1976
The hydroxylation of p-tyramine in manR A Jones, R J Pollitt
The Biochemical Journal|July 1, 1972
Glycoasparagines in the urine of patients with aspartylglycosaminuriaR J Pollitt, K M Pretty
Journal of Chromatography|March 1, 1978
The determination of 5-methoxyindole-3-acetic acid in human urine by mass fragmentographyJ A Hoskins, R J Pollitt
Archives Francaises De Pediatrie|January 1, 1987
[Attitude of parents toward the prenatal diagnosis of phenylketonuria]B E Barwell, R J Pollitt
The Biochemical Journal|January 1, 1972
New derivatives of argininosuccinic acid in the urine of a patient with argininosuccinicaciduriaC R Lee, R J Pollitt
Pageof 14