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Resultados da Busca: Foram encontrado(s) 172 registro(s)

Fam BSO, Reales G, Vargas-Pinilla P, Paré P, Viscardi LH, Sortica VA, Felkl AB, de O Franco Á, Lucion AB, Costa-Neto CM, Pissinatti A, Salzano FM, Paixão-Côrtes VR, Bortolini MC.

AVPR1b variation and the emergence of adaptive phenotypes in Platyrrhini primates.

Castilhos RM, Santos JAD, Augustin MC, Pedroso JL, Barsottini O, Saba R, Ferraz HB, Godeiro Junior C, Vargas FR, Salarini DZ, Furtado GV, Polese-Bonatto M, Rodrigues LP, Sena LS, Saraiva-Pereira ML, Jardim LB; RedeNeurogenética

Minimal prevalence of Huntington’s disease in the South of Brazil and instability of the expanded CAG tract
during intergenerational transmissions

Martins C, de Medeiros PFV, Leistner-Segal S, Dridi L, Elcioglu N, Wood J, Behnam M, Noyan B, Lacerda L, Geraghty MT, Labuda D, Giugliani R, Pshezhetsky AV

Molecular characterization of a large group of Mucopolysaccharidosis type IIIC patients reveals the
evolutionary history of the disease

Giugliani L, Vanzella C, Zambrano MB, Donis KC, Wallau TKW, Costa FMD, Giugliani R.

Clinical research challenges in rare genetic diseases in Brazil.

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