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B Udd

Showing results (11-20 of 54) with videos related to

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Neuromuscular Disorders : NMD|June 1, 1997
Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?B Udd, R Krahe, C Wallgren-Pettersson, et al.
European Journal of Neurology|April 24, 2010
Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patientsA-L Kaivorinne, J Krüger, B Udd, et al.
Neurology|September 26, 2001
Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish familyM Rantamäki, R Krahe, A Paetau, et al.
European Journal of Neurology|December 4, 2008
Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degenerationJ Krüger, A-L Kaivorinne, B Udd, et al.
Journal of Neuromuscular Diseases|November 18, 2016
GNE-Myopathy in a Greek Romani Family with Unusual Calf Phenotype and Protein Aggregation PathologyG K Papadimas, A Evilä, C Papadopoulos, et al.
American Journal of Human Genetics|April 29, 1998
Assignment of the tibial muscular dystrophy locus to chromosome 2q31H Haravuori, P Mäkelä-Bengs, B Udd, et al.
Neurology|July 1, 2011
Late-onset lower motor neuronopathy: a new autosomal dominant disorderM Jokela, S Penttilä, S Huovinen, et al.
Acta Neurologica Belgica|April 9, 2014
Laing early-onset distal myopathy in a Belgian familyP Y K Van den Bergh, J J Martin, F Lecouvet, et al.
Acta Neurologica Scandinavica|September 2, 1998
High prevalence of Kennedy's disease in Western Finland -- is the syndrome underdiagnosed?B Udd, V Juvonen, L Hakamies, et al.
Clinical Genetics|September 27, 2007
Do carriers of POLG mutation W748S have disease manifestations?M Rantamäki, P Luoma, J J Virta, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Neuromuscular Disorders : NMD|June 1, 1997
Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?B Udd, R Krahe, C Wallgren-Pettersson, et al.
European Journal of Neurology|April 24, 2010
Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patientsA-L Kaivorinne, J Krüger, B Udd, et al.
Neurology|September 26, 2001
Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish familyM Rantamäki, R Krahe, A Paetau, et al.
European Journal of Neurology|December 4, 2008
Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degenerationJ Krüger, A-L Kaivorinne, B Udd, et al.
Journal of Neuromuscular Diseases|November 18, 2016
GNE-Myopathy in a Greek Romani Family with Unusual Calf Phenotype and Protein Aggregation PathologyG K Papadimas, A Evilä, C Papadopoulos, et al.
American Journal of Human Genetics|April 29, 1998
Assignment of the tibial muscular dystrophy locus to chromosome 2q31H Haravuori, P Mäkelä-Bengs, B Udd, et al.
Neurology|July 1, 2011
Late-onset lower motor neuronopathy: a new autosomal dominant disorderM Jokela, S Penttilä, S Huovinen, et al.
Acta Neurologica Belgica|April 9, 2014
Laing early-onset distal myopathy in a Belgian familyP Y K Van den Bergh, J J Martin, F Lecouvet, et al.
Acta Neurologica Scandinavica|September 2, 1998
High prevalence of Kennedy's disease in Western Finland -- is the syndrome underdiagnosed?B Udd, V Juvonen, L Hakamies, et al.
Clinical Genetics|September 27, 2007
Do carriers of POLG mutation W748S have disease manifestations?M Rantamäki, P Luoma, J J Virta, et al.
Pageof 6