Search research articles
Contact Us
Filters
Showing results (51-60 of 54) with videos related to
Page
of 6
Sort By:
You have reached the last page of results.
This site can display upto 54 results.
European Journal of Human Genetics : EJHG
|
July 4, 2001
Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world
A Lund, B Udd, V Juvonen, et al.
European Journal of Neurology
|
February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families
P H Jonson, J Palmio, M Johari, et al.
Neurology
|
September 4, 2008
Distinct muscle imaging patterns in myofibrillar myopathies
D Fischer, R A Kley, K Strach, et al.
Revue Neurologique
|
September 7, 2015
Myofibrillar myopathies: State of the art, present and future challenges
A Béhin, E Salort-Campana, K Wahbi, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 54) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 54 results.
European Journal of Human Genetics : EJHG
|
July 4, 2001
Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world
A Lund, B Udd, V Juvonen, et al.
European Journal of Neurology
|
February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families
P H Jonson, J Palmio, M Johari, et al.
Neurology
|
September 4, 2008
Distinct muscle imaging patterns in myofibrillar myopathies
D Fischer, R A Kley, K Strach, et al.
Revue Neurologique
|
September 7, 2015
Myofibrillar myopathies: State of the art, present and future challenges
A Béhin, E Salort-Campana, K Wahbi, et al.
Page
of 6