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International Journal of Health Geographics
|
June 21, 2014
Modelling environmental factors correlated with podoconiosis: a geospatial study of non-filarial elephantiasis
Yordanos 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 database
Jorge 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 seizures
Philippa 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 evaluation
Daniel 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 trial
Daniel 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 Recommendations
Clara 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 infection
Yanick J Crow, Andrea Leitch, Bruce E Hayward, et al.
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of 9
Search research articles
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Showing results (71-80 of 82) with videos related to
Sort By:
Page
of 9
International Journal of Health Geographics
|
June 21, 2014
Modelling environmental factors correlated with podoconiosis: a geospatial study of non-filarial elephantiasis
Yordanos 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 database
Jorge 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 seizures
Philippa 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 evaluation
Daniel 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 trial
Daniel 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 Recommendations
Clara 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 infection
Yanick J Crow, Andrea Leitch, Bruce E Hayward, et al.
Page
of 9