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Acta Neuropathologica
|
January 29, 2010
Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibers
Olayinka 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 patients
Johanna 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 fibromyalgia
Satu 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 patients
Hanna-Kaisa Mentula, Laura Tuovinen, Sini Penttilä, et al.
Neuromuscular Disorders : NMD
|
July 4, 2012
Camptocormia as presenting sign in myofibrillar myopathy
Dimitri 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 family
Johanna 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 patient
Odile 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 Finland
Tiina Suominen, Linda L Bachinski, Satu Auvinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
November 23, 2006
[Not Available]
Olayinka Raheem, Tiina Suominen, Peter Hackman, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Acta Neuropathologica
|
January 29, 2010
Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibers
Olayinka 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 patients
Johanna 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 fibromyalgia
Satu 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 patients
Hanna-Kaisa Mentula, Laura Tuovinen, Sini Penttilä, et al.
Neuromuscular Disorders : NMD
|
July 4, 2012
Camptocormia as presenting sign in myofibrillar myopathy
Dimitri 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 family
Johanna 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 patient
Odile 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 Finland
Tiina Suominen, Linda L Bachinski, Satu Auvinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
November 23, 2006
[Not Available]
Olayinka Raheem, Tiina Suominen, Peter Hackman, et al.
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of 3