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Manu Jokela

Showing results (11-20 of 47) with videos related to

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Clinical Rheumatology|April 29, 2026
Increasing recognition of statin-associated anti-HMGCR antibody-positive autoimmune myopathy: a single-center retrospective studyMikko Mali, Laura Pirilä, Manu Jokela, et al.
Journal of Neuromuscular Diseases|October 30, 2018
Homozygous Nonsense Mutation p.Q274X in TRIM63 (MuRF1) in a Patient with Mild Skeletal Myopathy and Cardiac HypertrophyManu Jokela, Peter Baumann, Sanna Huovinen, 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.
European Journal of Human Genetics : EJHG|April 27, 2012
Autosomal dominant late-onset spinal motor neuronopathy is linked to a new locus on chromosome 22q11.2-q13.2Sini Penttilä, Manu Jokela, Peter Hackman, et al.
Annals of Neurology|November 28, 2014
Late onset spinal motor neuronopathy is caused by mutation in CHCHD10Sini Penttilä, Manu Jokela, Heidi Bouquin, et al.
Neuromuscular Disorders : NMD|July 12, 2017
Gluteus maximus hypertrophy: A diagnostic clue in four and a half LIM domain 1-mutated reducing body myopathyManu Jokela, Sanna Huovinen, Johanna Palmio, et al.
Neurology|September 7, 2023
<i>CACNA1S</i> Variant Associated With a Myalgic Myopathy PhenotypeVesa Periviita, Johanna Palmio, Manu Jokela, et al.
European Journal of Neurology|February 17, 2026
Over-Representation of TTN Truncating Variants in a Finnish Cohort of Patients With Axial MyopathyMaria Francesca Di Feo, Giuliana Capece, Marco Savarese, et al.
Plos One|March 22, 2016
Distinct Muscle Biopsy Findings in Genetically Defined Adult-Onset Motor Neuron DisordersManu Jokela, Sanna Huovinen, Olayinka Raheem, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Clinical Rheumatology|April 29, 2026
Increasing recognition of statin-associated anti-HMGCR antibody-positive autoimmune myopathy: a single-center retrospective studyMikko Mali, Laura Pirilä, Manu Jokela, et al.
Journal of Neuromuscular Diseases|October 30, 2018
Homozygous Nonsense Mutation p.Q274X in TRIM63 (MuRF1) in a Patient with Mild Skeletal Myopathy and Cardiac HypertrophyManu Jokela, Peter Baumann, Sanna Huovinen, 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.
European Journal of Human Genetics : EJHG|April 27, 2012
Autosomal dominant late-onset spinal motor neuronopathy is linked to a new locus on chromosome 22q11.2-q13.2Sini Penttilä, Manu Jokela, Peter Hackman, et al.
Annals of Neurology|November 28, 2014
Late onset spinal motor neuronopathy is caused by mutation in CHCHD10Sini Penttilä, Manu Jokela, Heidi Bouquin, et al.
Neuromuscular Disorders : NMD|July 12, 2017
Gluteus maximus hypertrophy: A diagnostic clue in four and a half LIM domain 1-mutated reducing body myopathyManu Jokela, Sanna Huovinen, Johanna Palmio, et al.
Neurology|September 7, 2023
<i>CACNA1S</i> Variant Associated With a Myalgic Myopathy PhenotypeVesa Periviita, Johanna Palmio, Manu Jokela, et al.
European Journal of Neurology|February 17, 2026
Over-Representation of TTN Truncating Variants in a Finnish Cohort of Patients With Axial MyopathyMaria Francesca Di Feo, Giuliana Capece, Marco Savarese, et al.
Plos One|March 22, 2016
Distinct Muscle Biopsy Findings in Genetically Defined Adult-Onset Motor Neuron DisordersManu Jokela, Sanna Huovinen, Olayinka Raheem, et al.
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