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Peter Baxter

Showing results (71-80 of 82) with videos related to

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International Journal of Health Geographics|June 21, 2014
Modelling environmental factors correlated with podoconiosis: a geospatial study of non-filarial elephantiasisYordanos B Molla, Nicola A Wardrop, Jennifer S Le Blond, et al.
European Journal of Human Genetics : EJHG|September 13, 2012
Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific databaseJorge Oliveira, Márcia E Oliveira, Wolfram Kress, et al.
Nursing Standard (Royal College of Nursing (Great Britain) : 1987)|September 30, 2016
protecting the patient or just playing politics?James Noak, Moyra Baldwin, Sally Black, et al.
Nature Medicine|February 24, 2006
Mutations in antiquitin in individuals with pyridoxine-dependent seizuresPhilippa B Mills, Eduard Struys, Cornelis Jakobs, et al.
Archives of Disease in Childhood|October 20, 2018
Surveillance for variant CJD: should more children with neurodegenerative diseases have autopsies?Christopher Verity, Anne Marie Winstone, Robert Will, et al.
Health Technology Assessment (Winchester, England)|June 20, 2017
Aquatic therapy for children with Duchenne muscular dystrophy: a pilot feasibility randomised controlled trial and mixed-methods process evaluationDaniel Hind, James Parkin, Victoria Whitworth, et al.
Pilot and Feasibility Studies|March 31, 2017
Aquatic therapy for boys with Duchenne muscular dystrophy (DMD): an external pilot randomised controlled trialDaniel Hind, James Parkin, Victoria Whitworth, et al.
Brain : a Journal of Neurology|June 18, 2010
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)Philippa B Mills, Emma J Footitt, Kevin A Mills, et al.
JIMD Reports|April 22, 2014
Lysine-Restricted Diet as Adjunct Therapy for Pyridoxine-Dependent Epilepsy: The PDE Consortium Consensus RecommendationsClara D M van Karnebeek, Sylvia Stockler-Ipsiroglu, Sravan Jaggumantri, et al.
Nature Genetics|July 18, 2006
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infectionYanick J Crow, Andrea Leitch, Bruce E Hayward, et al.
Pageof 9

Showing results (71-80 of 82) with videos related to

Sort By:
Pageof 9
International Journal of Health Geographics|June 21, 2014
Modelling environmental factors correlated with podoconiosis: a geospatial study of non-filarial elephantiasisYordanos B Molla, Nicola A Wardrop, Jennifer S Le Blond, et al.
European Journal of Human Genetics : EJHG|September 13, 2012
Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific databaseJorge Oliveira, Márcia E Oliveira, Wolfram Kress, et al.
Nursing Standard (Royal College of Nursing (Great Britain) : 1987)|September 30, 2016
protecting the patient or just playing politics?James Noak, Moyra Baldwin, Sally Black, et al.
Nature Medicine|February 24, 2006
Mutations in antiquitin in individuals with pyridoxine-dependent seizuresPhilippa B Mills, Eduard Struys, Cornelis Jakobs, et al.
Archives of Disease in Childhood|October 20, 2018
Surveillance for variant CJD: should more children with neurodegenerative diseases have autopsies?Christopher Verity, Anne Marie Winstone, Robert Will, et al.
Health Technology Assessment (Winchester, England)|June 20, 2017
Aquatic therapy for children with Duchenne muscular dystrophy: a pilot feasibility randomised controlled trial and mixed-methods process evaluationDaniel Hind, James Parkin, Victoria Whitworth, et al.
Pilot and Feasibility Studies|March 31, 2017
Aquatic therapy for boys with Duchenne muscular dystrophy (DMD): an external pilot randomised controlled trialDaniel Hind, James Parkin, Victoria Whitworth, et al.
Brain : a Journal of Neurology|June 18, 2010
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)Philippa B Mills, Emma J Footitt, Kevin A Mills, et al.
JIMD Reports|April 22, 2014
Lysine-Restricted Diet as Adjunct Therapy for Pyridoxine-Dependent Epilepsy: The PDE Consortium Consensus RecommendationsClara D M van Karnebeek, Sylvia Stockler-Ipsiroglu, Sravan Jaggumantri, et al.
Nature Genetics|July 18, 2006
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infectionYanick J Crow, Andrea Leitch, Bruce E Hayward, et al.
Pageof 9