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W Padberg

Showing results (201-210 of 228) with videos related to

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Human Molecular Genetics|July 21, 1998
Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosisR J Lemmers, S M van der Maarel, J C van Deutekom, et al.
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.
American Journal of Human Genetics|January 13, 2000
De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10S M van der Maarel, G Deidda, R J Lemmers, 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.
Journal of Medical Genetics|November 3, 2004
FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patientsT Rijkers, G Deidda, S van Koningsbruggen, 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.
Pageof 23

Showing results (201-210 of 228) with videos related to

Sort By:
Pageof 23
Human Molecular Genetics|July 21, 1998
Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosisR J Lemmers, S M van der Maarel, J C van Deutekom, et al.
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.
American Journal of Human Genetics|January 13, 2000
De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10S M van der Maarel, G Deidda, R J Lemmers, 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.
Journal of Medical Genetics|November 3, 2004
FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patientsT Rijkers, G Deidda, S van Koningsbruggen, 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.
Pageof 23