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American Journal of Medical Genetics
|
December 10, 1999
Jeune syndrome and liver disease: report of three cases treated with ursodeoxycholic acid
P Labrune, M Fabre, P Trioche, et al.
Neurology
|
October 10, 2001
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study
Y He, K J Jones, N Vignier, et al.
Neuromuscular Disorders : NMD
|
October 6, 2005
134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The Netherlands
E Bertini, A Burghes, K Bushby, et al.
European Journal of Neurology
|
October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies
R Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Page
of 2
Search research articles
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Showing results (11-20 of 14) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 14 results.
American Journal of Medical Genetics
|
December 10, 1999
Jeune syndrome and liver disease: report of three cases treated with ursodeoxycholic acid
P Labrune, M Fabre, P Trioche, et al.
Neurology
|
October 10, 2001
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study
Y He, K J Jones, N Vignier, et al.
Neuromuscular Disorders : NMD
|
October 6, 2005
134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The Netherlands
E Bertini, A Burghes, K Bushby, et al.
European Journal of Neurology
|
October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies
R Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Page
of 2