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Mostrando ítems 231-240 de 476
Indicaciones y utilidad de la inmunoglobulina por vía intravenosa en el manejo de polimiositis refractaria. Reporte de caso y revisión de la literatura
(Universidad Militar Nueva Granada, 2010)
Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenital (Becker disease) carrying a new mutation in the CLCN1 gene
(Revista de Biología Tropical 56(1) p.1-11, 2006-08-18)
Myotonia congenita is a muscular disease characterized by myotonia, hypertrophy, and stiffness. It
is inherited as either autosomal dominant or recessive known as Thomsen and Becker diseases, respectively.
Here we confirm ...
Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenital (Becker disease) carrying a new mutation in the CLCN1 gene
(Revista de Biología Tropical 56(1) p.1-11, 2006-08-18)
Myotonia congenita is a muscular disease characterized by myotonia, hypertrophy, and stiffness. It
is inherited as either autosomal dominant or recessive known as Thomsen and Becker diseases, respectively.
Here we confirm ...
Miastenia gravis en pediatría
(Sociedad Chilena de Pediatría, 2005)
Miastenia Gravis en canino, reporte de caso.
(Unilasallista Corporación Universitaria, 2023)