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George W Padberg

Showing results (11-20 of 46) with videos related to

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Journal of Neurology|December 4, 2003
Oculopharyngeal muscular dystrophy with limb girdle weakness as major complaintBarbara M Van Der Sluijs, Lies H Hoefsloot, George W Padberg, et al.
Genomics|June 15, 2005
Identifying new candidate genes for hereditary facial paresis on chromosome 3q21-q22 by RNA in situ hybridization in mouseBert van der Zwaag, J Peter H Burbach, Curt Scharfe, et al.
Neuromuscular Disorders : NMD|March 31, 2009
Quantitative MR imaging of individual muscle involvement in facioscapulohumeral muscular dystrophyHermien E Kan, Tom W J Scheenen, Marielle Wohlgemuth, et al.
Neuromuscular Disorders : NMD|June 24, 2026
A portrait of facioscapulohumeral muscular dystrophy through history: past milestones and future challenges on the road to understanding and treatmentAnna Greco, George W Padberg, Kees van de Graaf, et al.
Annals of Neurology|June 3, 2004
Somatic mosaicism in FSHD often goes undetectedRichard J L F Lemmers, Michiel J R van der Wielen, Egbert Bakker, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 22, 2007
Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collectionCarolien G F de Kovel, Barbara Franke, Frans A Hol, et al.
Neuromuscular Disorders : NMD|October 22, 2018
Experiences with bariatric surgery in patients with facioscapulohumeral dystrophy and myotonic dystrophy type 1: A qualitative studyEsther E D H Abel, Edith H C Cup, Anke Lanser, et al.
Nature Genetics|October 2, 2002
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomereRichard J L F Lemmers, Peggy de Kievit, Lodewijk Sandkuijl, et al.
American Journal of Human Genetics|May 22, 2004
Mechanism and timing of mitotic rearrangements in the subtelomeric D4Z4 repeat involved in facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Petra G M Van Overveld, Lodewijk A Sandkuijl, et al.
Pediatric Neurology|August 11, 2004
Sequence analysis of the PLEXIN-D1 gene in Möbius syndrome patientsBert van der Zwaag, Harriette T F M Verzijl, Karin H Wichers, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Journal of Neurology|December 4, 2003
Oculopharyngeal muscular dystrophy with limb girdle weakness as major complaintBarbara M Van Der Sluijs, Lies H Hoefsloot, George W Padberg, et al.
Genomics|June 15, 2005
Identifying new candidate genes for hereditary facial paresis on chromosome 3q21-q22 by RNA in situ hybridization in mouseBert van der Zwaag, J Peter H Burbach, Curt Scharfe, et al.
Neuromuscular Disorders : NMD|March 31, 2009
Quantitative MR imaging of individual muscle involvement in facioscapulohumeral muscular dystrophyHermien E Kan, Tom W J Scheenen, Marielle Wohlgemuth, et al.
Neuromuscular Disorders : NMD|June 24, 2026
A portrait of facioscapulohumeral muscular dystrophy through history: past milestones and future challenges on the road to understanding and treatmentAnna Greco, George W Padberg, Kees van de Graaf, et al.
Annals of Neurology|June 3, 2004
Somatic mosaicism in FSHD often goes undetectedRichard J L F Lemmers, Michiel J R van der Wielen, Egbert Bakker, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 22, 2007
Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collectionCarolien G F de Kovel, Barbara Franke, Frans A Hol, et al.
Neuromuscular Disorders : NMD|October 22, 2018
Experiences with bariatric surgery in patients with facioscapulohumeral dystrophy and myotonic dystrophy type 1: A qualitative studyEsther E D H Abel, Edith H C Cup, Anke Lanser, et al.
Nature Genetics|October 2, 2002
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomereRichard J L F Lemmers, Peggy de Kievit, Lodewijk Sandkuijl, et al.
American Journal of Human Genetics|May 22, 2004
Mechanism and timing of mitotic rearrangements in the subtelomeric D4Z4 repeat involved in facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Petra G M Van Overveld, Lodewijk A Sandkuijl, et al.
Pediatric Neurology|August 11, 2004
Sequence analysis of the PLEXIN-D1 gene in Möbius syndrome patientsBert van der Zwaag, Harriette T F M Verzijl, Karin H Wichers, et al.
Pageof 5