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P Treacy

Showing results (61-70 of 100) with videos related to

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Molecular Genetics and Metabolism|September 2, 2014
Systemic gene dysregulation in classical Galactosaemia: Is there a central mechanism?K P Coss, E P Treacy, E J Cotter, et al.
Molecular Genetics and Metabolism|September 10, 1999
Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohortB R Akerman, H Lemass, L M Chow, et al.
The Journal of Pediatrics|February 3, 2009
Outcomes of siblings with classical galactosemiaJoanne Hughes, Stephanie Ryan, Deborah Lambert, et al.
Irish Medical Journal|December 6, 2006
Mitochondrial cytopathies, phenotypic heterogeneity and a high incidenceE Ryan, M D King, P Rustin, et al.
Irish Journal of Medical Science|May 26, 2017
A template for reducing ophthalmology outpatient waiting times: community ophthalmic careR K Goetz, F E Hughes, E S Duignan, et al.
JIMD Reports|June 27, 2019
The genetic and biochemical basis of trimethylaminuria in an Irish cohortSamantha Doyle, James J O'Byrne, Mandy Nesbitt, et al.
Pediatric Research|December 3, 2009
Galactosemia, a single gene disorder with epigenetic consequencesDavid J Coman, David W Murray, Jennifer C Byrne, et al.
JIMD Reports|October 1, 2015
IgG N-Glycosylation Galactose Incorporation Ratios for the Monitoring of Classical GalactosaemiaHenning Stockmann, Karen P Coss, M Estela Rubio-Gozalbo, et al.
The Journal of Pediatrics|August 10, 2000
Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family studyE P Treacy, D M Lambert, R Barnes, et al.
Food Science & Nutrition|November 9, 2022
Determination of the lactose and galactose content of common foods: Relevance to galactosemiaLoai A Shakerdi, Leonie Wallace, Georgina Smyth, et al.
Pageof 10

Showing results (61-70 of 100) with videos related to

Sort By:
Pageof 10
Molecular Genetics and Metabolism|September 2, 2014
Systemic gene dysregulation in classical Galactosaemia: Is there a central mechanism?K P Coss, E P Treacy, E J Cotter, et al.
Molecular Genetics and Metabolism|September 10, 1999
Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohortB R Akerman, H Lemass, L M Chow, et al.
The Journal of Pediatrics|February 3, 2009
Outcomes of siblings with classical galactosemiaJoanne Hughes, Stephanie Ryan, Deborah Lambert, et al.
Irish Medical Journal|December 6, 2006
Mitochondrial cytopathies, phenotypic heterogeneity and a high incidenceE Ryan, M D King, P Rustin, et al.
Irish Journal of Medical Science|May 26, 2017
A template for reducing ophthalmology outpatient waiting times: community ophthalmic careR K Goetz, F E Hughes, E S Duignan, et al.
JIMD Reports|June 27, 2019
The genetic and biochemical basis of trimethylaminuria in an Irish cohortSamantha Doyle, James J O'Byrne, Mandy Nesbitt, et al.
Pediatric Research|December 3, 2009
Galactosemia, a single gene disorder with epigenetic consequencesDavid J Coman, David W Murray, Jennifer C Byrne, et al.
JIMD Reports|October 1, 2015
IgG N-Glycosylation Galactose Incorporation Ratios for the Monitoring of Classical GalactosaemiaHenning Stockmann, Karen P Coss, M Estela Rubio-Gozalbo, et al.
The Journal of Pediatrics|August 10, 2000
Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family studyE P Treacy, D M Lambert, R Barnes, et al.
Food Science & Nutrition|November 9, 2022
Determination of the lactose and galactose content of common foods: Relevance to galactosemiaLoai A Shakerdi, Leonie Wallace, Georgina Smyth, et al.
Pageof 10