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Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: Seven new mutations
(Wiley-Blackwell, 2004-04-01)
We have studied the molecular genetics of 27 Brazilian families with ataxia telangiectasia (AT). Five founder effect haplotypes accounted for 55.5% of the families. AT is an autosomal recessive disorder of childhood onset ...
Avaliação do polimorfismo da Ala16ValMnSOD e dos parâmetros bioquímicos no déficit cognitivo na epilepsia
(Universidade Federal de Santa MariaBrasilFarmacologiaUFSMPrograma de Pós-Graduação em FarmacologiaCentro de Ciências da Saúde, 2020-03-09)
Epilepsy is a chronic neurological condition, characterized by recurrent epileptic
seizures that can cause neurochemical, cognitive and psychological changes. The
mechanisms of action associated with epilepsy can involve ...
Fascículo longitudinal inferior: una nueva mirada del lenguaje
(Sociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la Salud, 2016-12-01)