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Showing results (181-190 of 228) with videos related to

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Annals of Neurology|September 24, 2005
Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophyPetra G M van Overveld, Leo Enthoven, Enzo Ricci, et al.
International Journal of Radiation Oncology, Biology, Physics|July 1, 1994
The choice of treatment of single brain metastasis should be based on extracranial tumor activity and ageE M Noordijk, C J Vecht, H Haaxma-Reiche, 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.
Annals of Neurology|June 1, 1993
Treatment of single brain metastasis: radiotherapy alone or combined with neurosurgery?C J Vecht, H Haaxma-Reiche, E M Noordijk, et al.
American Journal of Human Genetics|August 1, 1992
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qterC Wijmenga, L A Sandkuijl, P Moerer, 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.
Gene|August 6, 1999
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb elementJ Gabriëls, M C Beckers, H Ding, 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|September 2, 2014
Skeletal muscle imaging in facioscapulohumeral muscular dystrophy, pattern and asymmetry of individual muscle involvementN H M Rijken, E L van der Kooi, J C M Hendriks, 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.
Pageof 23

Showing results (181-190 of 228) with videos related to

Sort By:
Pageof 23
Annals of Neurology|September 24, 2005
Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophyPetra G M van Overveld, Leo Enthoven, Enzo Ricci, et al.
International Journal of Radiation Oncology, Biology, Physics|July 1, 1994
The choice of treatment of single brain metastasis should be based on extracranial tumor activity and ageE M Noordijk, C J Vecht, H Haaxma-Reiche, 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.
Annals of Neurology|June 1, 1993
Treatment of single brain metastasis: radiotherapy alone or combined with neurosurgery?C J Vecht, H Haaxma-Reiche, E M Noordijk, et al.
American Journal of Human Genetics|August 1, 1992
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qterC Wijmenga, L A Sandkuijl, P Moerer, 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.
Gene|August 6, 1999
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb elementJ Gabriëls, M C Beckers, H Ding, 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|September 2, 2014
Skeletal muscle imaging in facioscapulohumeral muscular dystrophy, pattern and asymmetry of individual muscle involvementN H M Rijken, E L van der Kooi, J C M Hendriks, 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.
Pageof 23