Results 71 to 80 of about 234 (144)
Hirayama Disease: Case Report. [PDF]
Rodrigues VA +3 more
europepmc +1 more source
[Parkinson-dementia and amyotrophic lateral sclerosis association (complex of Guam). Diagnostic challenge, Mexican patient]. [PDF]
Aguilar-Vázquez CA +4 more
europepmc +1 more source
Atrofia Muscular Espinal: La Realidad del Paciente Adulto en España
Atrofia muscular espinal; Enfermedades neuromusculares; Registro de ...
De Lemus, Mencía +3 more
openaire +2 more sources
La terapia génica de la atrofia muscular espinal. Una revisión sistemática
La atrofia muscular espinal es una enfermedad hereditaria crónica y degenerativa con una alta incidencia en la población, con una morbimortalidad elevada en pacientes pediátricos y elevados costes de recursos sanitarios en pacientes que llegan a la edad adulta. Las aparición de terapias génicas como Onasemnogene abeparvovec (Zolgensma) pueden modificar
openaire +1 more source
[Spinal Muscular Atrophy: The Reality of the Adult Patient in Spain]. [PDF]
Cattinari MG +3 more
europepmc +1 more source
[Use of disease-modifying therapies in spinal muscular atrophy 5q in Mexico]. [PDF]
Meza-Cano ME, Molina-Castillo C.
europepmc +1 more source
['Wait and see' in paediatric epilepsy. Our experience]. [PDF]
Salinas-Salvador B +5 more
europepmc +1 more source
Atrofia Muscular Espinal: la vida diaria con una enfermedad neuromuscular.
This Final Degree Project (FDP) presentation aims to do a theoretical approach about Spinal Muscular Atrophy (SMA), a little-known hereditary neuromuscular disease which study has increased in recent years in the search for a treatment that improves quality of life of affected people.
openaire +1 more source
Effectiveness of Risdiplam Treatment in Adult Patients With Spinal Muscular Atrophy Type IIb-III. [PDF]
García Estévez DA.
europepmc +1 more source

