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George W Padberg

Showing results (31-40 of 46) with videos related to

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Clinical Genetics|September 14, 2018
Phenotype-genotype relations in facioscapulohumeral muscular dystrophy type 1Karlien Mul, Nicol C Voermans, Richard J L F Lemmers, et al.
BMC Neurology|October 15, 2013
Determining the role of sarcomeric proteins in facioscapulohumeral muscular dystrophy: a study protocolSaskia Lassche, Coen A C Ottenheijm, Nicol C Voermans, et al.
Neuromuscular Disorders : NMD|November 6, 2017
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient dataRianne J M Goselink, Nicol C Voermans, Kees Okkersen, et al.
Nature Genetics|November 25, 2003
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophyPetra G M van Overveld, Richard J F L Lemmers, Lodewijk A Sandkuijl, et al.
Neurology|October 15, 2017
Adding quantitative muscle MRI to the FSHD clinical trial toolboxKarlien Mul, Sanne C C Vincenten, Nicol C Voermans, et al.
American Journal of Human Genetics|October 10, 2007
Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Marielle Wohlgemuth, Kristiaan J van der Gaag, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 14, 2018
A 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophyRianne J M Goselink, Caroline R van Kernebeek, Karlien Mul, 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.
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.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Clinical Genetics|September 14, 2018
Phenotype-genotype relations in facioscapulohumeral muscular dystrophy type 1Karlien Mul, Nicol C Voermans, Richard J L F Lemmers, et al.
BMC Neurology|October 15, 2013
Determining the role of sarcomeric proteins in facioscapulohumeral muscular dystrophy: a study protocolSaskia Lassche, Coen A C Ottenheijm, Nicol C Voermans, et al.
Neuromuscular Disorders : NMD|November 6, 2017
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient dataRianne J M Goselink, Nicol C Voermans, Kees Okkersen, et al.
Nature Genetics|November 25, 2003
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophyPetra G M van Overveld, Richard J F L Lemmers, Lodewijk A Sandkuijl, et al.
Neurology|October 15, 2017
Adding quantitative muscle MRI to the FSHD clinical trial toolboxKarlien Mul, Sanne C C Vincenten, Nicol C Voermans, et al.
American Journal of Human Genetics|October 10, 2007
Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Marielle Wohlgemuth, Kristiaan J van der Gaag, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 14, 2018
A 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophyRianne J M Goselink, Caroline R van Kernebeek, Karlien Mul, 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.
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.
Pageof 5