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E Treacy

Showing results (1-10 of 16) with videos related to

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American Journal of Human Genetics|February 1, 1995
Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparisonE Treacy, B Childs, C R Scriver
Journal of Perinatology : Official Journal of the California Perinatal Association|January 31, 2003
Pancreatic pseudocysts in pregnancy: a case report and review of the literatureJennifer J Eddy, Gerald E Lynch, Deborah E Treacy
European Journal of Human Genetics : EJHG|January 1, 1993
'Celtic' phenylketonuria chromosomes found? Evidence in two regions of Quebec ProvinceE Treacy, S Byck, C Clow, et al.
The Journal of Pediatrics|March 1, 1993
Methylmalonic acidemia with a severe chemical but benign clinical phenotypeE Treacy, C Clow, O A Mamer, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Trimethylaminuria, fish odour syndrome: a new method of detection and response to treatment with metronidazoleE Treacy, D Johnson, J J Pitt, et al.
Pediatric Neurology|November 1, 1996
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome)M I Shevell, P Colangelo, E Treacy, et al.
Atherosclerosis|March 20, 2001
Fenofibrate raises plasma homocysteine levels in the fasted and fed statesR Bissonnette, E Treacy, R Rozen, et al.
Prenatal Diagnosis|July 1, 1997
Prenatal diagnosis for inborn errors of metabolism and haemoglobinopathies: the Montreal Children's Hospital experienceK Sasi, D Sanderson, P Eydoux, et al.
American Journal of Human Genetics|December 18, 1997
Human phenylalanine hydroxylase mutations and hyperphenylalaninemia phenotypes: a metanalysis of genotype-phenotype correlationsE Kayaalp, E Treacy, P J Waters, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
In vivo disposal of phenylalanine in phenylketonuria: a study of two siblingsE Treacy, J J Pitt, K Seller, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
American Journal of Human Genetics|February 1, 1995
Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparisonE Treacy, B Childs, C R Scriver
Journal of Perinatology : Official Journal of the California Perinatal Association|January 31, 2003
Pancreatic pseudocysts in pregnancy: a case report and review of the literatureJennifer J Eddy, Gerald E Lynch, Deborah E Treacy
European Journal of Human Genetics : EJHG|January 1, 1993
'Celtic' phenylketonuria chromosomes found? Evidence in two regions of Quebec ProvinceE Treacy, S Byck, C Clow, et al.
The Journal of Pediatrics|March 1, 1993
Methylmalonic acidemia with a severe chemical but benign clinical phenotypeE Treacy, C Clow, O A Mamer, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Trimethylaminuria, fish odour syndrome: a new method of detection and response to treatment with metronidazoleE Treacy, D Johnson, J J Pitt, et al.
Pediatric Neurology|November 1, 1996
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome)M I Shevell, P Colangelo, E Treacy, et al.
Atherosclerosis|March 20, 2001
Fenofibrate raises plasma homocysteine levels in the fasted and fed statesR Bissonnette, E Treacy, R Rozen, et al.
Prenatal Diagnosis|July 1, 1997
Prenatal diagnosis for inborn errors of metabolism and haemoglobinopathies: the Montreal Children's Hospital experienceK Sasi, D Sanderson, P Eydoux, et al.
American Journal of Human Genetics|December 18, 1997
Human phenylalanine hydroxylase mutations and hyperphenylalaninemia phenotypes: a metanalysis of genotype-phenotype correlationsE Kayaalp, E Treacy, P J Waters, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
In vivo disposal of phenylalanine in phenylketonuria: a study of two siblingsE Treacy, J J Pitt, K Seller, et al.
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