Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Peter Hackman

Showing results (11-20 of 82) with videos related to

Pageof 9
Sort By:
Duodecim; Laaketieteellinen Aikakauskirja|June 17, 2003
[A new type of myotonic dystrophy]Satu Auvinen, Anna Vihola, Ralf Krahe, et al.
The Journal of Molecular Diagnostics : JMD|November 17, 2019
Improving Copy Number Variant Detection from Sequencing Data with a Combination of Programs and a Predictive ModelSalla Välipakka, Marco Savarese, Lydia Sagath, et al.
Skeletal Muscle|March 31, 2018
The complexity of titin splicing pattern in human adult skeletal musclesMarco Savarese, Per Harald Jonson, Sanna Huovinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 14, 2003
[Respiratory arrests caused by congenital myasthenia gravis syndrome]Roger F Byring, Kinji Ohno, Helena Pihko, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 5, 2010
The enigma of 7q36 linked autosomal dominant limb girdle muscular dystrophySatu Sandell, Sanna Huovinen, Jaakko Sarparanta, et al.
Plos One|March 13, 2014
Gene expression profiling in tibial muscular dystrophy reveals unfolded protein response and altered autophagyMark Screen, Olayinka Raheem, Jeanette Holmlund-Hampf, et al.
Neuromuscular Disorders : NMD|August 24, 2014
Isolated semitendinosus involvement in the initial stages of limb-girdle muscular dystrophy 2LGiorgio Tasca, Anni Evilä, Marika Pane, et al.
Pediatric Research|February 14, 2014
Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadismJohanna Känsäkoski, Rainer Fagerholm, Eeva-Maria Laitinen, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|January 18, 2021
Panorama of the distal myopathiesMarco Savarese, Jaakko Sarparanta, Anna Vihola, et al.
Neuromuscular Disorders : NMD|June 21, 2011
Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish familyJohanna Palmio, Satu Sandell, Tiina Suominen, et al.
Pageof 9

Showing results (11-20 of 82) with videos related to

Sort By:
Pageof 9
Duodecim; Laaketieteellinen Aikakauskirja|June 17, 2003
[A new type of myotonic dystrophy]Satu Auvinen, Anna Vihola, Ralf Krahe, et al.
The Journal of Molecular Diagnostics : JMD|November 17, 2019
Improving Copy Number Variant Detection from Sequencing Data with a Combination of Programs and a Predictive ModelSalla Välipakka, Marco Savarese, Lydia Sagath, et al.
Skeletal Muscle|March 31, 2018
The complexity of titin splicing pattern in human adult skeletal musclesMarco Savarese, Per Harald Jonson, Sanna Huovinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 14, 2003
[Respiratory arrests caused by congenital myasthenia gravis syndrome]Roger F Byring, Kinji Ohno, Helena Pihko, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 5, 2010
The enigma of 7q36 linked autosomal dominant limb girdle muscular dystrophySatu Sandell, Sanna Huovinen, Jaakko Sarparanta, et al.
Plos One|March 13, 2014
Gene expression profiling in tibial muscular dystrophy reveals unfolded protein response and altered autophagyMark Screen, Olayinka Raheem, Jeanette Holmlund-Hampf, et al.
Neuromuscular Disorders : NMD|August 24, 2014
Isolated semitendinosus involvement in the initial stages of limb-girdle muscular dystrophy 2LGiorgio Tasca, Anni Evilä, Marika Pane, et al.
Pediatric Research|February 14, 2014
Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadismJohanna Känsäkoski, Rainer Fagerholm, Eeva-Maria Laitinen, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|January 18, 2021
Panorama of the distal myopathiesMarco Savarese, Jaakko Sarparanta, Anna Vihola, et al.
Neuromuscular Disorders : NMD|June 21, 2011
Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish familyJohanna Palmio, Satu Sandell, Tiina Suominen, et al.
Pageof 9