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M Tuchman

Showing results (61-70 of 112) with videos related to

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Pediatrics|February 1, 1985
Value of random urinary homovanillic acid and vanillylmandelic acid levels in the diagnosis and management of patients with neuroblastoma: comparison with 24-hour urine collectionsM Tuchman, C L Morris, M L Ramnaraine, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
The biochemical and molecular spectrum of ornithine transcarbamylase deficiencyM Tuchman, H Morizono, B S Rajagopal, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1991
X-chromosome inactivation in the liver of female heterozygous OTC-deficient sparse-furash miceJ D Mrozek, R A Holzknecht, R J Butkowski, et al.
Journal of Inherited Metabolic Disease|July 13, 2004
Fatal presentation of ornithine transcarbamylase deficiency in a 62-year-old man and family studiesT Rohininath, D J Costello, T Lynch, et al.
Clinical Biochemistry|June 1, 1987
Determination of urinary homovanillic and vanillylmandelic acids from dried filter paper samples: assessment of potential methods for neuroblastoma screeningM Tuchman, C Auray-Blais, M L Ramnaraine, et al.
Enzyme|January 1, 1989
Dihydropyrimidine dehydrogenase activity in human blood mononuclear cellsM Tuchman, R V Roemeling, W A Hrushesky, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Allopurinol challenge test in childrenA B Burlina, V Ferrari, C Dionisi-Vici, et al.
Pediatric Research|November 1, 1992
Six new mutations in the ornithine transcarbamylase gene detected by single-strand conformational polymorphismM Tuchman, R A Holzknecht, A B Gueron, et al.
The American Journal of Pediatric Hematology/Oncology|May 1, 1994
Persistence and possible progression of a pelvic neuroblastoma detected by mass screening during 19 monthsM L Bernstein, E M Azouz, W Woods, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1992
Screening urine of 3-week-old newborns: transient methylmalonic and hydroxyphenyllactic aciduriaM Tuchman, M T McCann, M M Thompson, et al.
Pageof 12

Showing results (61-70 of 112) with videos related to

Sort By:
Pageof 12
Pediatrics|February 1, 1985
Value of random urinary homovanillic acid and vanillylmandelic acid levels in the diagnosis and management of patients with neuroblastoma: comparison with 24-hour urine collectionsM Tuchman, C L Morris, M L Ramnaraine, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
The biochemical and molecular spectrum of ornithine transcarbamylase deficiencyM Tuchman, H Morizono, B S Rajagopal, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1991
X-chromosome inactivation in the liver of female heterozygous OTC-deficient sparse-furash miceJ D Mrozek, R A Holzknecht, R J Butkowski, et al.
Journal of Inherited Metabolic Disease|July 13, 2004
Fatal presentation of ornithine transcarbamylase deficiency in a 62-year-old man and family studiesT Rohininath, D J Costello, T Lynch, et al.
Clinical Biochemistry|June 1, 1987
Determination of urinary homovanillic and vanillylmandelic acids from dried filter paper samples: assessment of potential methods for neuroblastoma screeningM Tuchman, C Auray-Blais, M L Ramnaraine, et al.
Enzyme|January 1, 1989
Dihydropyrimidine dehydrogenase activity in human blood mononuclear cellsM Tuchman, R V Roemeling, W A Hrushesky, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Allopurinol challenge test in childrenA B Burlina, V Ferrari, C Dionisi-Vici, et al.
Pediatric Research|November 1, 1992
Six new mutations in the ornithine transcarbamylase gene detected by single-strand conformational polymorphismM Tuchman, R A Holzknecht, A B Gueron, et al.
The American Journal of Pediatric Hematology/Oncology|May 1, 1994
Persistence and possible progression of a pelvic neuroblastoma detected by mass screening during 19 monthsM L Bernstein, E M Azouz, W Woods, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1992
Screening urine of 3-week-old newborns: transient methylmalonic and hydroxyphenyllactic aciduriaM Tuchman, M T McCann, M M Thompson, et al.
Pageof 12