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

Tiina Suominen

Showing results (1-10 of 21) with videos related to

Pageof 3
Sort By:
Acta Neuropathologica|January 29, 2010
Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibersOlayinka Raheem, Sanna Huovinen, Tiina Suominen, 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.
Arthritis and Rheumatism|November 1, 2008
Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgiaSatu Auvinen, Tiina Suominen, Pekka Hannonen, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 26, 2012
TARDBP mutations are not a frequent cause of ALS in Finnish patientsHanna-Kaisa Mentula, Laura Tuovinen, Sini Penttilä, et al.
Neuromuscular Disorders : NMD|July 4, 2012
Camptocormia as presenting sign in myofibrillar myopathyDimitri Renard, Giovanni Castelnovo, Carla Fernandez, 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.
Journal of Neurology|February 1, 2011
A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patientOdile Dubourg, Thierry Maisonobe, Anthony Behin, et al.
European Journal of Human Genetics : EJHG|March 3, 2011
Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in FinlandTiina Suominen, Linda L Bachinski, Satu Auvinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|November 23, 2006
[Not Available]Olayinka Raheem, Tiina Suominen, Peter Hackman, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Acta Neuropathologica|January 29, 2010
Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibersOlayinka Raheem, Sanna Huovinen, Tiina Suominen, 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.
Arthritis and Rheumatism|November 1, 2008
Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgiaSatu Auvinen, Tiina Suominen, Pekka Hannonen, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 26, 2012
TARDBP mutations are not a frequent cause of ALS in Finnish patientsHanna-Kaisa Mentula, Laura Tuovinen, Sini Penttilä, et al.
Neuromuscular Disorders : NMD|July 4, 2012
Camptocormia as presenting sign in myofibrillar myopathyDimitri Renard, Giovanni Castelnovo, Carla Fernandez, 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.
Journal of Neurology|February 1, 2011
A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patientOdile Dubourg, Thierry Maisonobe, Anthony Behin, et al.
European Journal of Human Genetics : EJHG|March 3, 2011
Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in FinlandTiina Suominen, Linda L Bachinski, Satu Auvinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|November 23, 2006
[Not Available]Olayinka Raheem, Tiina Suominen, Peter Hackman, et al.
Pageof 3