Buscar
Mostrando ítems 101-104 de 104
Centronuclear myopathy: histopathological aspects in ten patients with chilfhood onset
(Academia Brasileira de Neurologia - ABNEURO, 1998-03-01)
Centronuclear myopathy is a rare congenital myopathy. According to the period of onset of signs and symptoms and the degree of muscular involvement three clinical forms are distinguished: severe neonatal; childhood onset; ...
Estudo da miotonia hereditária em suínos
(Universidade Estadual Paulista (Unesp), 2018-07-10)
A principal causa de miotonia não distrófica hereditária ocorre devido à mutações no gene CLCN1, codificante para a proteína CLC1 que forma o canal iônico seletivo para o íon cloreto predominante no tecido muscular ...
The role of cugbp1 in the development of zebrafish lens
(Instituto Tecnólogico de Costa Rica. Escuela de Biología, 2012)
The lens is a transparent tissue in the anterior of the eye and its main role is to refract light on the retina.
The lens consists of two types of cells: epithelial cells and fibers. Epithelial cells surround the anterior ...