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G W Padberg

Showing results (91-100 of 114) with videos related to

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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.
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.
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.
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.
Neurology|August 25, 2004
Strength training and albuterol in facioscapulohumeral muscular dystrophyE L van der Kooi, O J M Vogels, R J G P van Asseldonk, et al.
Cytogenetics and Cell Genetics|June 1, 2000
Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35M van Geel, J C van Deutekom, A van Staalduinen, et al.
Human Molecular Genetics|May 1, 1996
Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35J C van Deutekom, R J Lemmers, P K Grewal, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlationsM R Nelen, H Kremer, I B Konings, et al.
Neurology|October 15, 2003
Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 allelesM Wohlgemuth, R J Lemmers, E L van der Kooi, et al.
Pageof 12

Showing results (91-100 of 114) with videos related to

Sort By:
Pageof 12
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.
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.
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.
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.
Neurology|August 25, 2004
Strength training and albuterol in facioscapulohumeral muscular dystrophyE L van der Kooi, O J M Vogels, R J G P van Asseldonk, et al.
Cytogenetics and Cell Genetics|June 1, 2000
Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35M van Geel, J C van Deutekom, A van Staalduinen, et al.
Human Molecular Genetics|May 1, 1996
Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35J C van Deutekom, R J Lemmers, P K Grewal, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlationsM R Nelen, H Kremer, I B Konings, et al.
Neurology|October 15, 2003
Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 allelesM Wohlgemuth, R J Lemmers, E L van der Kooi, et al.
Pageof 12