Detalles de la búsqueda
1.
Forelimb treatment in a large cohort of dystrophic dogs supports delivery of a recombinant AAV for exon skipping in Duchenne patients.
Mol Ther
; 22(11): 1923-35, 2014 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-25200009
2.
Wrist flexion and extension torques measured by highly sensitive dynamometer in healthy subjects from 5 to 80 years.
BMC Musculoskelet Disord
; 16: 4, 2015 Jan 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-25636264
3.
Ankle dorsi- and plantar-flexion torques measured by dynamometry in healthy subjects from 5 to 80 years.
BMC Musculoskelet Disord
; 14: 104, 2013 Mar 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-23522186
4.
A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment.
PLoS One
; 11(6): e0156696, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27271157
5.
Relationship between muscle impairments, postural stability, and gait parameters assessed with lower-trunk accelerometry in myotonic dystrophy type 1.
Neuromuscul Disord
; 26(7): 428-35, 2016 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-27234310
6.
Longitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy.
Neurology
; 86(11): 1022-30, 2016 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-26888987
7.
NMR imaging estimates of muscle volume and intramuscular fat infiltration in the thigh: variations with muscle, gender, and age.
Age (Dordr)
; 37(3): 9798, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-26040416
8.
Upper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial.
PLoS One
; 10(4): e0121799, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-25861036
9.
Upper limb strength and function changes during a one-year follow-up in non-ambulant patients with Duchenne Muscular Dystrophy: an observational multicenter trial.
PLoS One
; 10(2): e0113999, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-25643053
10.
Non-Ambulant Duchenne Patients Theoretically Treatable by Exon 53 Skipping have Severe Phenotype.
J Neuromuscul Dis
; 2(3): 269-279, 2015 Sep 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-27858743
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