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David Hilton

Showing results (111-120 of 130) with videos related to

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Journal of Neurology|April 12, 2017
The UK Myotonic Dystrophy Patient Registry: facilitating and accelerating clinical researchLibby Wood, Isabell Cordts, Antonio Atalaia, et al.
Neurology|May 13, 2016
Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weaknessZoltan Lukacs, Paulina Nieves Cobos, Stephan Wenninger, et al.
Neurology|July 31, 2019
Idiopathic inflammatory myopathy: Interrater variability in muscle biopsy readingPieter A Olivier, Boel De Paepe, Eleonora Aronica, et al.
BMJ (Clinical Research Ed.)|November 18, 2010
Open letter to prime minister David Cameron and health secretary Andrew LansleyDavid J Nicholl, David Hilton-Jones, Jacqueline Palace, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 20, 2011
Clinical Dutch-English Lambert-Eaton Myasthenic syndrome (LEMS) tumor association prediction score accurately predicts small-cell lung cancer in the LEMSMaarten J Titulaer, Paul Maddison, Jacob K Sont, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathyAlexey Shatunov, Montse Olivé, Zagaa Odgerel, et al.
Nature Genetics|May 4, 2004
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathyJoy Irobi, Katrien Van Impe, Pavel Seeman, et al.
Brain : a Journal of Neurology|May 13, 2010
Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathiesMagdalena Zimoń, Jonathan Baets, Michaela Auer-Grumbach, et al.
Neurobiology of Aging|February 12, 2015
The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositisQiang Gang, Conceicao Bettencourt, Pedro M Machado, et al.
Nature Genetics|May 4, 2004
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathyOleg V Evgrafov, Irena Mersiyanova, Joy Irobi, et al.
Pageof 13

Showing results (111-120 of 130) with videos related to

Sort By:
Pageof 13
Journal of Neurology|April 12, 2017
The UK Myotonic Dystrophy Patient Registry: facilitating and accelerating clinical researchLibby Wood, Isabell Cordts, Antonio Atalaia, et al.
Neurology|May 13, 2016
Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weaknessZoltan Lukacs, Paulina Nieves Cobos, Stephan Wenninger, et al.
Neurology|July 31, 2019
Idiopathic inflammatory myopathy: Interrater variability in muscle biopsy readingPieter A Olivier, Boel De Paepe, Eleonora Aronica, et al.
BMJ (Clinical Research Ed.)|November 18, 2010
Open letter to prime minister David Cameron and health secretary Andrew LansleyDavid J Nicholl, David Hilton-Jones, Jacqueline Palace, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 20, 2011
Clinical Dutch-English Lambert-Eaton Myasthenic syndrome (LEMS) tumor association prediction score accurately predicts small-cell lung cancer in the LEMSMaarten J Titulaer, Paul Maddison, Jacob K Sont, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathyAlexey Shatunov, Montse Olivé, Zagaa Odgerel, et al.
Nature Genetics|May 4, 2004
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathyJoy Irobi, Katrien Van Impe, Pavel Seeman, et al.
Brain : a Journal of Neurology|May 13, 2010
Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathiesMagdalena Zimoń, Jonathan Baets, Michaela Auer-Grumbach, et al.
Neurobiology of Aging|February 12, 2015
The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositisQiang Gang, Conceicao Bettencourt, Pedro M Machado, et al.
Nature Genetics|May 4, 2004
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathyOleg V Evgrafov, Irena Mersiyanova, Joy Irobi, et al.
Pageof 13