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Bjarne Udd

Showing results (41-50 of 255) with videos related to

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Journal of the Neurological Sciences|February 5, 2022
Scapuloperoneal syndrome with mitochondrial DNA deletionÉmilie Pichette, Erin O'Ferrall, Jason Karamchandani, et al.
Duodecim; Laaketieteellinen Aikakauskirja|December 5, 2002
[New adult-onset ataxia in a Finnish family]Maria Rantamäki, Ralf Krahe, Anders Paetau, et al.
Muscle & Nerve|December 23, 2011
Pain in patients with myotonic dystrophy type 2: a postal survey in FinlandKimmo I Suokas, Maija Haanpää, Hannu Kautiainen, et al.
Neuromuscular Disorders : NMD|April 9, 2021
Novel TNNT1 mutation and mild nemaline myopathy phenotype in an Italian patientAntonio Petrucci, Guido Primiano, Marco Savarese, et al.
Duodecim; Laaketieteellinen Aikakauskirja|November 14, 2013
[The expanding spectrum of LGMD--recently discovered disease genes are important also in Finnish patients]Manu Jokela, Johanna Palmio, Satu Sandell, et al.
Duodecim; Laaketieteellinen Aikakauskirja|December 1, 2017
Distal myopathies in Finnish patientsJohanna Palmio, Manu Jokela, Satu Sandell, et al.
Clinical Case Reports|December 17, 2016
Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix-Saguenay, ARSACS, in a Finnish familyJohanna Palmio, Mikko Kärppä, Peter Baumann, et al.
Journal of Molecular Biology|March 6, 2007
Haploinsuffciency for Znf9 in Znf9+/- mice is associated with multiorgan abnormalities resembling myotonic dystrophyWei Chen, Yucheng Wang, Yoko Abe, et al.
Neuromuscular Disorders : NMD|July 23, 2014
Screening for late-onset Pompe disease in FinlandJohanna Palmio, Mari Auranen, Sari Kiuru-Enari, et al.
Neurology|March 24, 2017
Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in <i>SCN4A</i> geneJohanna Palmio, Satu Sandell, Michael G Hanna, et al.
Pageof 26

Showing results (41-50 of 255) with videos related to

Sort By:
Pageof 26
Journal of the Neurological Sciences|February 5, 2022
Scapuloperoneal syndrome with mitochondrial DNA deletionÉmilie Pichette, Erin O'Ferrall, Jason Karamchandani, et al.
Duodecim; Laaketieteellinen Aikakauskirja|December 5, 2002
[New adult-onset ataxia in a Finnish family]Maria Rantamäki, Ralf Krahe, Anders Paetau, et al.
Muscle & Nerve|December 23, 2011
Pain in patients with myotonic dystrophy type 2: a postal survey in FinlandKimmo I Suokas, Maija Haanpää, Hannu Kautiainen, et al.
Neuromuscular Disorders : NMD|April 9, 2021
Novel TNNT1 mutation and mild nemaline myopathy phenotype in an Italian patientAntonio Petrucci, Guido Primiano, Marco Savarese, et al.
Duodecim; Laaketieteellinen Aikakauskirja|November 14, 2013
[The expanding spectrum of LGMD--recently discovered disease genes are important also in Finnish patients]Manu Jokela, Johanna Palmio, Satu Sandell, et al.
Duodecim; Laaketieteellinen Aikakauskirja|December 1, 2017
Distal myopathies in Finnish patientsJohanna Palmio, Manu Jokela, Satu Sandell, et al.
Clinical Case Reports|December 17, 2016
Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix-Saguenay, ARSACS, in a Finnish familyJohanna Palmio, Mikko Kärppä, Peter Baumann, et al.
Journal of Molecular Biology|March 6, 2007
Haploinsuffciency for Znf9 in Znf9+/- mice is associated with multiorgan abnormalities resembling myotonic dystrophyWei Chen, Yucheng Wang, Yoko Abe, et al.
Neuromuscular Disorders : NMD|July 23, 2014
Screening for late-onset Pompe disease in FinlandJohanna Palmio, Mari Auranen, Sari Kiuru-Enari, et al.
Neurology|March 24, 2017
Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in <i>SCN4A</i> geneJohanna Palmio, Satu Sandell, Michael G Hanna, et al.
Pageof 26