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M Enns

Showing results (91-100 of 208) with videos related to

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Eclinicalmedicine|January 31, 2024
Efficacy and safety of pegzilarginase in arginase 1 deficiency (PEACE): a phase 3, randomized, double-blind, placebo-controlled, multi-centre trialRossana Sanchez Russo, Serena Gasperini, Gillian Bubb, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|May 11, 2013
A new LC-MS/MS method for the clinical determination of reduced and oxidized glutathione from whole bloodTereza Moore, Anthony Le, Anna-Kaisa Niemi, et al.
Journal of Animal Science|May 29, 2015
Optimum measurement period for evaluating feed intake traits in beef cattleM M Culbertson, S E Speidel, R K Peel, et al.
Genetics and Molecular Research : GMR|May 1, 2007
Associations of DNA polymorphisms in growth hormone and its transcriptional regulators with growth and carcass traits in two populations of Brangus bullsM G Thomas, R M Enns, K L Shirley, et al.
Molecular Genetics and Metabolism|March 1, 2015
Long-term safety and efficacy of sapropterin: the PKUDOS registry experienceNicola Longo, Georgianne L Arnold, Gabriella Pridjian, et al.
American Journal of Medical Genetics. Part A|June 9, 2006
Genitopatellar syndrome: expanding the phenotype and excluding mutations in LMX1B and TBX4Omar A Abdul-Rahman, Trang H La, Andrea Kwan, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 19, 2009
Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemiaKondala R Atkuri, Tina M Cowan, Tony Kwan, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 9, 2009
Novel deoxyguanosine kinase gene mutations and viral infection predispose apparently healthy children to fulminant liver failureJoseph T C Shieh, William E Berquist, Qing Zhang, et al.
Clinical Genetics|September 7, 2005
Relationship of primary mitochondrial respiratory chain dysfunction to fiber type abnormalities in skeletal muscleG M Enns, C L Hoppel, S J DeArmond, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
Methotrexate/misoprostol embryopathy: report of four cases resulting from failed medical abortionMargaret P Adam, Melanie A Manning, Anita E Beck, et al.
Pageof 21

Showing results (91-100 of 208) with videos related to

Sort By:
Pageof 21
Eclinicalmedicine|January 31, 2024
Efficacy and safety of pegzilarginase in arginase 1 deficiency (PEACE): a phase 3, randomized, double-blind, placebo-controlled, multi-centre trialRossana Sanchez Russo, Serena Gasperini, Gillian Bubb, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|May 11, 2013
A new LC-MS/MS method for the clinical determination of reduced and oxidized glutathione from whole bloodTereza Moore, Anthony Le, Anna-Kaisa Niemi, et al.
Journal of Animal Science|May 29, 2015
Optimum measurement period for evaluating feed intake traits in beef cattleM M Culbertson, S E Speidel, R K Peel, et al.
Genetics and Molecular Research : GMR|May 1, 2007
Associations of DNA polymorphisms in growth hormone and its transcriptional regulators with growth and carcass traits in two populations of Brangus bullsM G Thomas, R M Enns, K L Shirley, et al.
Molecular Genetics and Metabolism|March 1, 2015
Long-term safety and efficacy of sapropterin: the PKUDOS registry experienceNicola Longo, Georgianne L Arnold, Gabriella Pridjian, et al.
American Journal of Medical Genetics. Part A|June 9, 2006
Genitopatellar syndrome: expanding the phenotype and excluding mutations in LMX1B and TBX4Omar A Abdul-Rahman, Trang H La, Andrea Kwan, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 19, 2009
Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemiaKondala R Atkuri, Tina M Cowan, Tony Kwan, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 9, 2009
Novel deoxyguanosine kinase gene mutations and viral infection predispose apparently healthy children to fulminant liver failureJoseph T C Shieh, William E Berquist, Qing Zhang, et al.
Clinical Genetics|September 7, 2005
Relationship of primary mitochondrial respiratory chain dysfunction to fiber type abnormalities in skeletal muscleG M Enns, C L Hoppel, S J DeArmond, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
Methotrexate/misoprostol embryopathy: report of four cases resulting from failed medical abortionMargaret P Adam, Melanie A Manning, Anita E Beck, et al.
Pageof 21