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Bjarne Udd

Showing results (11-20 of 255) with videos related to

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The Lancet. Neurology|September 22, 2012
The myotonic dystrophies: molecular, clinical, and therapeutic challengesBjarne Udd, Ralf Krahe
Neuromuscular Disorders : NMD|January 24, 2018
Hereditary myopathy with early respiratory failure (HMERF): Still rare, but common enoughGiorgio Tasca, Bjarne Udd
Journal of Molecular Neuroscience : MN|November 18, 2015
Diagnostic Clinical, Electrodiagnostic and Muscle Pathology Features of Spinal and Bulbar Muscular AtrophyManu E Jokela, Bjarne Udd
Annals of Neurology|June 23, 2015
Reply: To PMID 25428574Manu Jokela, Sini Penttilä, Bjarne Udd
Duodecim; Laaketieteellinen Aikakauskirja|September 2, 2005
[The kinase domain of titin controls muscle gene expression and protein turnover]Peter Hackman, Anna Vihola, Bjarne Udd
Neuromuscular Disorders : NMD|July 30, 2018
229th ENMC international workshop: Limb girdle muscular dystrophies - Nomenclature and reformed classification Naarden, the Netherlands, 17-19 March 2017Volker Straub, Alexander Murphy, Bjarne Udd, et al.
Neuromuscular Disorders : NMD|August 25, 2011
Double trouble: spinal muscular atrophy type II and seropositive myasthenia gravis in the same patientManu Jokela, Bjarne Udd, Markku Päivärinta
Handbook of Clinical Neurology|August 10, 2023
Distal myopathyMarco Savarese, Manu Jokela, Bjarne Udd
Journal of Neurology|May 15, 2016
Evolving neuromuscular phenotype in a patient with a heterozygous CHCHD10 p.G66V mutationManu E Jokela, Juho Joutsa, Bjarne Udd
Neuromuscular Disorders : NMD|November 15, 2018
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8-10 December 2017Conrad C Weihl, Bjarne Udd, Michael Hanna, et al.
Pageof 26

Showing results (11-20 of 255) with videos related to

Sort By:
Pageof 26
The Lancet. Neurology|September 22, 2012
The myotonic dystrophies: molecular, clinical, and therapeutic challengesBjarne Udd, Ralf Krahe
Neuromuscular Disorders : NMD|January 24, 2018
Hereditary myopathy with early respiratory failure (HMERF): Still rare, but common enoughGiorgio Tasca, Bjarne Udd
Journal of Molecular Neuroscience : MN|November 18, 2015
Diagnostic Clinical, Electrodiagnostic and Muscle Pathology Features of Spinal and Bulbar Muscular AtrophyManu E Jokela, Bjarne Udd
Annals of Neurology|June 23, 2015
Reply: To PMID 25428574Manu Jokela, Sini Penttilä, Bjarne Udd
Duodecim; Laaketieteellinen Aikakauskirja|September 2, 2005
[The kinase domain of titin controls muscle gene expression and protein turnover]Peter Hackman, Anna Vihola, Bjarne Udd
Neuromuscular Disorders : NMD|July 30, 2018
229th ENMC international workshop: Limb girdle muscular dystrophies - Nomenclature and reformed classification Naarden, the Netherlands, 17-19 March 2017Volker Straub, Alexander Murphy, Bjarne Udd, et al.
Neuromuscular Disorders : NMD|August 25, 2011
Double trouble: spinal muscular atrophy type II and seropositive myasthenia gravis in the same patientManu Jokela, Bjarne Udd, Markku Päivärinta
Handbook of Clinical Neurology|August 10, 2023
Distal myopathyMarco Savarese, Manu Jokela, Bjarne Udd
Journal of Neurology|May 15, 2016
Evolving neuromuscular phenotype in a patient with a heterozygous CHCHD10 p.G66V mutationManu E Jokela, Juho Joutsa, Bjarne Udd
Neuromuscular Disorders : NMD|November 15, 2018
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8-10 December 2017Conrad C Weihl, Bjarne Udd, Michael Hanna, et al.
Pageof 26