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W Padberg

Showing results (211-220 of 228) with videos related to

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Neuromuscular Disorders : NMD|September 29, 2006
No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophyE L van der Kooi, J C de Greef, M Wohlgemuth, et al.
Human Molecular Genetics|August 1, 1997
Germline mutations in the PTEN/MMAC1 gene in patients with Cowden diseaseM R Nelen, W C van Staveren, E A Peeters, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular DystrophyR W Tim, J R Gilbert, J M Stajich, et al.
Neurology|June 15, 2007
Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the familiesA J van der Kooi, W S Frankhuizen, P G Barth, et al.
Neurology|December 21, 2018
Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophyRianne J M Goselink, Karlien Mul, Caroline R van Kernebeek, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
Science (New York, N.Y.)|August 21, 2010
A unifying genetic model for facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Patrick J van der Vliet, Rinse Klooster, et al.
Plos Genetics|April 18, 2013
Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHDYvonne D Krom, Peter E Thijssen, Janet M Young, et al.
Neurology|October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2J C de Greef, R J L F Lemmers, P Camaño, et al.
Brain : a Journal of Neurology|October 1, 1996
The clinical spectrum of limb girdle muscular dystrophy. A survey in The NetherlandsA J van der Kooi, P G Barth, H F Busch, et al.
Pageof 23

Showing results (211-220 of 228) with videos related to

Sort By:
Pageof 23
Neuromuscular Disorders : NMD|September 29, 2006
No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophyE L van der Kooi, J C de Greef, M Wohlgemuth, et al.
Human Molecular Genetics|August 1, 1997
Germline mutations in the PTEN/MMAC1 gene in patients with Cowden diseaseM R Nelen, W C van Staveren, E A Peeters, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular DystrophyR W Tim, J R Gilbert, J M Stajich, et al.
Neurology|June 15, 2007
Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the familiesA J van der Kooi, W S Frankhuizen, P G Barth, et al.
Neurology|December 21, 2018
Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophyRianne J M Goselink, Karlien Mul, Caroline R van Kernebeek, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
Science (New York, N.Y.)|August 21, 2010
A unifying genetic model for facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Patrick J van der Vliet, Rinse Klooster, et al.
Plos Genetics|April 18, 2013
Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHDYvonne D Krom, Peter E Thijssen, Janet M Young, et al.
Neurology|October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2J C de Greef, R J L F Lemmers, P Camaño, et al.
Brain : a Journal of Neurology|October 1, 1996
The clinical spectrum of limb girdle muscular dystrophy. A survey in The NetherlandsA J van der Kooi, P G Barth, H F Busch, et al.
Pageof 23