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G W Padberg

Showing results (61-70 of 114) with videos related to

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Neurology|June 28, 2006
Dysphagia in facioscapulohumeral muscular dystrophyM Wohlgemuth, B J M de Swart, J G Kalf, et al.
NMR in Biomedicine|February 23, 2010
Only fat infiltrated muscles in resting lower leg of FSHD patients show disturbed energy metabolismH E Kan, D W J Klomp, M Wohlgemuth, et al.
Archives of Neurology|June 1, 1995
Molecular genetic reevaluation of the Dutch hyperekplexia familyM A Tijssen, R Shiang, J van Deutekom, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24A J van der Vleuten, C M van Ravenswaaij-Arts, C J Frijns, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 8, 2006
An unbiased and efficient computerised tomography method to quantify muscle and adipose tissue volume in neuromuscular patientsE L van der Kooi, G E de Leeuw, M H M Vlak, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 20, 2005
Experienced fatigue in facioscapulohumeral dystrophy, myotonic dystrophy, and HMSN-IJ S Kalkman, M L Schillings, S P van der Werf, et al.
Clinical Neuropathology|February 24, 2010
Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathyN C Voermans, M Guillard, R Doedée, et al.
Journal of Neurology|March 16, 2007
Effects of training and albuterol on pain and fatigue in facioscapulohumeral muscular dystrophyE L van der Kooi, J S Kalkman, E Lindeman, et al.
Muscle & Nerve. Supplement|April 12, 2013
Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35C Wijmenga, H G Dauwerse, G W Padberg, et al.
Journal of Medical Genetics|April 3, 2004
FRG1P is localised in the nucleolus, Cajal bodies, and specklesS van Koningsbruggen, R W Dirks, A M Mommaas, et al.
Pageof 12

Showing results (61-70 of 114) with videos related to

Sort By:
Pageof 12
Neurology|June 28, 2006
Dysphagia in facioscapulohumeral muscular dystrophyM Wohlgemuth, B J M de Swart, J G Kalf, et al.
NMR in Biomedicine|February 23, 2010
Only fat infiltrated muscles in resting lower leg of FSHD patients show disturbed energy metabolismH E Kan, D W J Klomp, M Wohlgemuth, et al.
Archives of Neurology|June 1, 1995
Molecular genetic reevaluation of the Dutch hyperekplexia familyM A Tijssen, R Shiang, J van Deutekom, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24A J van der Vleuten, C M van Ravenswaaij-Arts, C J Frijns, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 8, 2006
An unbiased and efficient computerised tomography method to quantify muscle and adipose tissue volume in neuromuscular patientsE L van der Kooi, G E de Leeuw, M H M Vlak, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 20, 2005
Experienced fatigue in facioscapulohumeral dystrophy, myotonic dystrophy, and HMSN-IJ S Kalkman, M L Schillings, S P van der Werf, et al.
Clinical Neuropathology|February 24, 2010
Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathyN C Voermans, M Guillard, R Doedée, et al.
Journal of Neurology|March 16, 2007
Effects of training and albuterol on pain and fatigue in facioscapulohumeral muscular dystrophyE L van der Kooi, J S Kalkman, E Lindeman, et al.
Muscle & Nerve. Supplement|April 12, 2013
Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35C Wijmenga, H G Dauwerse, G W Padberg, et al.
Journal of Medical Genetics|April 3, 2004
FRG1P is localised in the nucleolus, Cajal bodies, and specklesS van Koningsbruggen, R W Dirks, A M Mommaas, et al.
Pageof 12