Buscar
Mostrando ítems 1-10 de 584
Atrofia monomiélica distal de extremidad superior. Caso clínico
(Sociedad Médica de Santiago, Chile, 2021)
Monomelic amyotrophy, also known as Hirayama disease, is a rare lower
motor neuron syndrome due to localized lower motor neuron loss in the spinal
cord at the cervical level. Clinically, monomelic amyotrophy is defined ...
Dificuldades diagnósticas na atrofia muscular espinhalDiagnostic difficulties in spinal muscular atrophy
(Academia Brasileira de Neurologia, 2019)
Atrofia muscular espinal: Caracterización clínica, electrofisiológica y molecular de 26 pacientes
(Sociedad Médica de Santiago, 2011)
Teaching Video Neuroimages: Tongue Fasciculations In Spinal Muscular Atrophy
(LIPPINCOTT WILLIAMS & WILKINSPHILADELPHIA, 2015)
Physical Therapy Protocols to Attenuate Skeletal Muscle Atrophy in Critically ill Patients: Narrative Review
(SOC CHILENA ANATOMIA, 2022)
Características clínicas de los pacientes menores de 18 años con atrofia muscular espinal en Medellín, 2008 - 2013Clinical characteristics of patients under 18 years-old with spinal muscular atrophy in Medellín, 2008 – 2013
(Asociación Colombiana de NeurologíaGrupo de Investigación Clínica en Enfermedades del Niño y del Adolescente - PediacienciasBogotá, Colombia, 2021)
Detection of Spinal Muscular Atrophy Carriers in a Sample of the Brazilian Population
(KARGER, 2011)
Background: Spinal muscular atrophy is a common autosomal recessive neuromuscular disorder caused by mutations in the SMN1 gene. Identification of spinal muscular atrophy carriers has important implications for individuals ...