Results 71 to 80 of about 154 (136)

Distrofia Muscular de Duchenne

, 2015
The Duchenne muscular dystrophy is a genetic X-linked recessive disease. This is the most common form of muscular dystrophy in children, affecting 1 in 3500 newborn males (1). Together with the less aggressive form of muscular dystrophy (Becker’s dystrophy), these are the second most common hereditary disorders in humans (2). Genetically it is a defect
openaire   +1 more source

[Emergency implantation of a teleneurology service at the neuromuscular unit of Hospital Regional de Málaga during the SARS-CoV-2 pandemic]. [PDF]

Neurologia (Engl Ed), 2020
Romero-Imbroda J, Reyes-Garrido V, Ciano-Petersen NL, Serrano-Castro PJ.   +3 more
europepmc   +1 more source

Brazilian Society of Cardiology Guidelines on the Analysis and Issuance of Electrocardiographic Reports - 2022. [PDF]

Arq Bras Cardiol, 2022
Samesima N, God EG, Kruse JCL, Leal MG, Pinho C, França FFAC, Pimenta J, Cardoso AF, Paixão A, Fonseca A, Pérez-Riera AR, Ribeiro ALP, Madaloso BA, Luna Filho B, Oliveira CAR, Grupi CJ, Moreira DAR, Kaiser E, Paixão GMM, Feitosa Filho G, Pereira Filho HG, Grindler J, Aziz JL, Molina MS, Facin M, Tobias NMMO, Oliveira PA, Sanches PCR, Teixeira RA, Atanes SM, Pastore CA.   +30 more
europepmc   +1 more source

Ptose miogênica na distrofia muscular oculofaríngea

Revista Brasileira de Oftalmologia, 2016
RESUMO Relato de caso de distrofia muscular oculofaríngea, doença genética de herança autossômica dominante e uma das causas de ptose miogênica adquirida. A paciente apresentou quadro de ptose palpebral bilateral e disfagia, achados clínicos típicos da doença, foi submetida a tratamento cirúrgico da ptose, com bom resultado estético e funcional.
Hellen Cristina Paraguassu Macedo, José Ricardo Mouta Araújo, Roberto Freitas de Castro Leão, Gabriel Ângelo Ribeiro da Silva, Caroline Galvão Leite   +4 more
openaire   +1 more source

The heart-brain team: neurocardiology [PDF]

Arch Cardiol Mex, 2020
Jiménez-Ruiz A, Ruiz-Sandoval JL, Araiza-Garaygordobil D, Sierra-Lara D.   +3 more
europepmc   +1 more source

Asesoramiento genético preconcepcional a familia con hijo afectado de Distrofia Muscular de Duchenne Preconception Genetic Management to a family with a child affected by Duchenne Muscular Dystrophy

Revista Médica Electrónica, 2009
Las personas con discapacidad representan alrededor del 10 % de la población, por ello su atención va desde su prevención, mejorar su calidad de vida y la integración social.
Hilda Álvarez de la Campa Gil, Milaydi Moreira González, Dayri Falcón Rodríguez, Claribel Lugo Rodríguez   +3 more
doaj  

Atrialización de un caso de síndrome de aurícula paralítica Atrialization in one case of atrial palsy syndrome

Revista Colombiana de Cardiología, 2007
El síndrome de aurícula paralítica es una entidad poco común y generalmente se presenta aislada o asociada a trastornos degenerativos musculares. Se ha propuesto un mecanismo de transmisión familiar por transmisión autosómica dominante.
Alejandro Orjuela, Diego Vanegas, Juan de J Montenegro   +2 more
doaj  

[Autosomal recessive limb-girdle muscular dystrophy-10. Case report]. [PDF]

Rev Med Inst Mex Seguro Soc
Pérez-Arzola AA, Juárez-Melchor D, Crisanto-López IE, Vera-Loaiza A, Hernández-Castañeda Y, Guzmán-Santiago TA, Jiménez-Pérez B, Rodríguez-Hurtado PO, Salazar-Bonilla W.   +8 more
europepmc   +1 more source

[Benefits of ω-3 fatty acids in Duchenne muscular dystrophy]. [PDF]

Rev Med Inst Mex Seguro Soc
Galeazzi-Aguilar JE, Rodríguez-Cruz M.
europepmc   +1 more source

Understanding Cardiac Alterations in Familial Partial Lipodystrophy: Insights from Echocardiography. [PDF]

Arq Bras Cardiol
Barberato SH.
europepmc   +1 more source