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Bjarne Udd

Showing results (21-30 of 255) with videos related to

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Current Opinion in Neurology|July 17, 2024
Current advance on distal myopathy geneticsJohanna Ranta-Aho, Mridul Johari, Bjarne Udd
Journal of Cellular and Molecular Medicine|September 6, 2022
Use of animal models to understand titin physiology and pathologyMatteo Marcello, Viviana Cetrangolo, Marco Savarese, et al.
Brain : a Journal of Neurology|February 27, 2014
Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domainStephan Lange, Lars Edström, Bjarne Udd, et al.
Journal of Neurology|December 6, 2023
A retrospective study of accuracy and usefulness of electrophysiological exercise testsVesa Periviita, Manu Jokela, Johanna Palmio, et al.
Neuromuscular Disorders : NMD|December 3, 2015
Targeted next-generation sequencing assay for detection of mutations in primary myopathiesAnni Evilä, Meharji Arumilli, Bjarne Udd, et al.
BMJ Case Reports|April 26, 2015
When myopathy breaks the rules: a late-onset distal presentationRachel Newby, Stuart Jamieson, Bjarne Udd, et al.
Medecine Sciences : M/S|November 22, 2016
[Finland: an ideally valued genetic heritage]Bjarne Udd, Tuy Nga Brignol, J Andoni Urtizberea
Neuromuscular Disorders : NMD|February 19, 2017
219th ENMC International Workshop Titinopathies International database of titin mutations and phenotypes, Heemskerk, The Netherlands, 29 April-1 May 2016Peter Hackman, Bjarne Udd, Carsten G Bönnemann, et al.
Neuromuscular Disorders : NMD|January 22, 2002
Report of the 84th ENMC workshop: PROMM (proximal myotonic myopathy) and other myotonic dystrophy-like syndromes: 2nd workshop. 13-15th October, 2000, Loosdrecht, The NetherlandsRichard T Moxley, Giovanni Meola, Bjarne Udd, et al.
International Journal of Molecular Sciences|February 26, 2020
Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New ResultsJaakko Sarparanta, Per Harald Jonson, Sabita Kawan, et al.
Pageof 26

Showing results (21-30 of 255) with videos related to

Sort By:
Pageof 26
Current Opinion in Neurology|July 17, 2024
Current advance on distal myopathy geneticsJohanna Ranta-Aho, Mridul Johari, Bjarne Udd
Journal of Cellular and Molecular Medicine|September 6, 2022
Use of animal models to understand titin physiology and pathologyMatteo Marcello, Viviana Cetrangolo, Marco Savarese, et al.
Brain : a Journal of Neurology|February 27, 2014
Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domainStephan Lange, Lars Edström, Bjarne Udd, et al.
Journal of Neurology|December 6, 2023
A retrospective study of accuracy and usefulness of electrophysiological exercise testsVesa Periviita, Manu Jokela, Johanna Palmio, et al.
Neuromuscular Disorders : NMD|December 3, 2015
Targeted next-generation sequencing assay for detection of mutations in primary myopathiesAnni Evilä, Meharji Arumilli, Bjarne Udd, et al.
BMJ Case Reports|April 26, 2015
When myopathy breaks the rules: a late-onset distal presentationRachel Newby, Stuart Jamieson, Bjarne Udd, et al.
Medecine Sciences : M/S|November 22, 2016
[Finland: an ideally valued genetic heritage]Bjarne Udd, Tuy Nga Brignol, J Andoni Urtizberea
Neuromuscular Disorders : NMD|February 19, 2017
219th ENMC International Workshop Titinopathies International database of titin mutations and phenotypes, Heemskerk, The Netherlands, 29 April-1 May 2016Peter Hackman, Bjarne Udd, Carsten G Bönnemann, et al.
Neuromuscular Disorders : NMD|January 22, 2002
Report of the 84th ENMC workshop: PROMM (proximal myotonic myopathy) and other myotonic dystrophy-like syndromes: 2nd workshop. 13-15th October, 2000, Loosdrecht, The NetherlandsRichard T Moxley, Giovanni Meola, Bjarne Udd, et al.
International Journal of Molecular Sciences|February 26, 2020
Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New ResultsJaakko Sarparanta, Per Harald Jonson, Sabita Kawan, et al.
Pageof 26