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George W Padberg

Showing results (21-30 of 46) with videos related to

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European Journal of Human Genetics : EJHG|August 17, 2006
Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genesCaroline B Michielse, Meena Bhat, Angela Brady, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|November 2, 2002
PLEXIN-D1, a novel plexin family member, is expressed in vascular endothelium and the central nervous system during mouse embryogenesisBert van der Zwaag, Anita J C G M Hellemons, William P J Leenders, et al.
Brain Communications|September 21, 2020
Ophthalmological findings in facioscapulohumeral dystrophyRianne J M Goselink, Vivian Schreur, Caroline R van Kernebeek, et al.
Annals of Neurology|September 24, 2005
Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophyPetra G M van Overveld, Leo Enthoven, Enzo Ricci, et al.
Neurology|July 13, 2018
A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1Mariëlle Wohlgemuth, Richard J Lemmers, Marianne Jonker, et al.
Muscle & Nerve|September 19, 2024
The other face of facioscapulohumeral muscular dystrophy: Exploring orofacial weakness using muscle ultrasoundSanne C C Vincenten, Jeroen L M van Doorn, Sjan Teeselink, et al.
Plos One|January 24, 2014
Distinct disease phases in muscles of facioscapulohumeral dystrophy patients identified by MR detected fat infiltrationBarbara H Janssen, Nicoline B M Voet, Christine I Nabuurs, et al.
Neurology|February 1, 2013
Sarcomeric dysfunction contributes to muscle weakness in facioscapulohumeral muscular dystrophySaskia Lassche, Ger J M Stienen, Tom C Irving, et al.
Neuromuscular Disorders : NMD|June 7, 2005
Recurrent somatic mosaicism for D4Z4 contractions in a family with facioscapulohumeral muscular dystrophyBorian T Buzhov, Richard J L F Lemmers, Ivailo Tournev, et al.
Neurology|August 15, 2014
Population-based incidence and prevalence of facioscapulohumeral dystrophyJohanna C W Deenen, Hisse Arnts, Silvère M van der Maarel, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
European Journal of Human Genetics : EJHG|August 17, 2006
Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genesCaroline B Michielse, Meena Bhat, Angela Brady, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|November 2, 2002
PLEXIN-D1, a novel plexin family member, is expressed in vascular endothelium and the central nervous system during mouse embryogenesisBert van der Zwaag, Anita J C G M Hellemons, William P J Leenders, et al.
Brain Communications|September 21, 2020
Ophthalmological findings in facioscapulohumeral dystrophyRianne J M Goselink, Vivian Schreur, Caroline R van Kernebeek, et al.
Annals of Neurology|September 24, 2005
Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophyPetra G M van Overveld, Leo Enthoven, Enzo Ricci, et al.
Neurology|July 13, 2018
A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1Mariëlle Wohlgemuth, Richard J Lemmers, Marianne Jonker, et al.
Muscle & Nerve|September 19, 2024
The other face of facioscapulohumeral muscular dystrophy: Exploring orofacial weakness using muscle ultrasoundSanne C C Vincenten, Jeroen L M van Doorn, Sjan Teeselink, et al.
Plos One|January 24, 2014
Distinct disease phases in muscles of facioscapulohumeral dystrophy patients identified by MR detected fat infiltrationBarbara H Janssen, Nicoline B M Voet, Christine I Nabuurs, et al.
Neurology|February 1, 2013
Sarcomeric dysfunction contributes to muscle weakness in facioscapulohumeral muscular dystrophySaskia Lassche, Ger J M Stienen, Tom C Irving, et al.
Neuromuscular Disorders : NMD|June 7, 2005
Recurrent somatic mosaicism for D4Z4 contractions in a family with facioscapulohumeral muscular dystrophyBorian T Buzhov, Richard J L F Lemmers, Ivailo Tournev, et al.
Neurology|August 15, 2014
Population-based incidence and prevalence of facioscapulohumeral dystrophyJohanna C W Deenen, Hisse Arnts, Silvère M van der Maarel, et al.
Pageof 5