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J Lawrence Merritt

Showing results (1-10 of 42) with videos related to

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Annals of Translational Medicine|February 12, 2019
Fatty acid oxidation disordersJ Lawrence Merritt, Marie Norris, Shibani Kanungo
Pediatric Nephrology (Berlin, Germany)|September 28, 2011
Newborn screening and renal disease: where we have been; where we are now; where we are goingJ Lawrence Merritt, David Askenazi, Si Houn Hahn
Journal of Inherited Metabolic Disease|July 30, 2009
A cognitively normal PDH-deficient 18-year-old man carrying the R263G mutation in the PDHA1 geneR Bachmann-Gagescu, J Lawrence Merritt, S H Hahn
Reviews in Endocrine & Metabolic Disorders|July 13, 2020
Clinical manifestations and management of fatty acid oxidation disordersJ Lawrence Merritt, Erin MacLeod, Agnieszka Jurecka, et al.
International Journal of Neonatal Screening|October 30, 2020
Considering Proximal Urea Cycle Disorders in Expanded Newborn ScreeningTania Vasquez-Loarte, John D Thompson, J Lawrence Merritt
Pediatric Neurology|October 22, 2013
Cystathionine beta-synthase deficiency heralded by cerebral sinus venous thrombosis and strokeIlene S Ruhoy, J Lawrence Merritt, Catherine Amlie-Lefond
Journal of Movement Disorders|May 25, 2022
Refractory Myoclonus as a Presentation of Metabolic Stroke in A Child With Cobalamin B Methylmalonic Acidemia After Liver and Kidney TransplantValerie Olson, Irene J Chang, J Lawrence Merritt, et al.
Molecular Genetics and Metabolism|April 29, 2018
Newborn screening for proximal urea cycle disorders: Current evidence supporting recommendations for newborn screeningJ Lawrence Merritt, Linnea L Brody, Gisele Pino, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 13, 2012
Next-generation sequencing for mitochondrial diseases: a wide diagnostic spectrumValeria Vasta, J Lawrence Merritt, Russell P Saneto, et al.
American Journal of Medical Genetics. Part A|February 17, 2007
Delineation of the cryptic 1qter deletion phenotypeJ Lawrence Merritt, Ying Zou, Syed M Jalal, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
Annals of Translational Medicine|February 12, 2019
Fatty acid oxidation disordersJ Lawrence Merritt, Marie Norris, Shibani Kanungo
Pediatric Nephrology (Berlin, Germany)|September 28, 2011
Newborn screening and renal disease: where we have been; where we are now; where we are goingJ Lawrence Merritt, David Askenazi, Si Houn Hahn
Journal of Inherited Metabolic Disease|July 30, 2009
A cognitively normal PDH-deficient 18-year-old man carrying the R263G mutation in the PDHA1 geneR Bachmann-Gagescu, J Lawrence Merritt, S H Hahn
Reviews in Endocrine & Metabolic Disorders|July 13, 2020
Clinical manifestations and management of fatty acid oxidation disordersJ Lawrence Merritt, Erin MacLeod, Agnieszka Jurecka, et al.
International Journal of Neonatal Screening|October 30, 2020
Considering Proximal Urea Cycle Disorders in Expanded Newborn ScreeningTania Vasquez-Loarte, John D Thompson, J Lawrence Merritt
Pediatric Neurology|October 22, 2013
Cystathionine beta-synthase deficiency heralded by cerebral sinus venous thrombosis and strokeIlene S Ruhoy, J Lawrence Merritt, Catherine Amlie-Lefond
Journal of Movement Disorders|May 25, 2022
Refractory Myoclonus as a Presentation of Metabolic Stroke in A Child With Cobalamin B Methylmalonic Acidemia After Liver and Kidney TransplantValerie Olson, Irene J Chang, J Lawrence Merritt, et al.
Molecular Genetics and Metabolism|April 29, 2018
Newborn screening for proximal urea cycle disorders: Current evidence supporting recommendations for newborn screeningJ Lawrence Merritt, Linnea L Brody, Gisele Pino, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 13, 2012
Next-generation sequencing for mitochondrial diseases: a wide diagnostic spectrumValeria Vasta, J Lawrence Merritt, Russell P Saneto, et al.
American Journal of Medical Genetics. Part A|February 17, 2007
Delineation of the cryptic 1qter deletion phenotypeJ Lawrence Merritt, Ying Zou, Syed M Jalal, et al.
Pageof 5