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Spinocerebellar ataxia
Spinocerebellar ataxia
Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism
China / Gait / Brain / Humans / Female / Spinocerebellar ataxia / Male / Proteins / Pedigree / Levodopa / Clinical Sciences / Aged / Middle Aged / Single Photon Emission Computed Tomography / Adult / Annals / Neurosciences / Spinocerebellar ataxia / Male / Proteins / Pedigree / Levodopa / Clinical Sciences / Aged / Middle Aged / Single Photon Emission Computed Tomography / Adult / Annals / Neurosciences
Spinocerebellar Ataxia Type 2 (SCA2): Clinical Features and Genetic Analysis
Adolescent / Rwanda / Movement disorders / Humans / Genetic Testing / Female / Spinocerebellar ataxia / Pedigree / Phenotype / Genetic Analysis / Ophthalmoplegia / Female / Spinocerebellar ataxia / Pedigree / Phenotype / Genetic Analysis / Ophthalmoplegia
Spinocerebellar Ataxia Type 2 (SCA2): Clinical Features and Genetic Analysis
Adolescent / Rwanda / Movement disorders / Humans / Genetic Testing / Female / Spinocerebellar ataxia / Pedigree / Phenotype / Genetic Analysis / Ophthalmoplegia / Female / Spinocerebellar ataxia / Pedigree / Phenotype / Genetic Analysis / Ophthalmoplegia
Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism
China / Gait / Brain / Humans / Female / Spinocerebellar ataxia / Male / Proteins / Pedigree / Levodopa / Clinical Sciences / Aged / Middle Aged / Single Photon Emission Computed Tomography / Adult / Annals / Neurosciences / Spinocerebellar ataxia / Male / Proteins / Pedigree / Levodopa / Clinical Sciences / Aged / Middle Aged / Single Photon Emission Computed Tomography / Adult / Annals / Neurosciences
Spinocerebellar Ataxia Type 2 (SCA2): Clinical Features and Genetic Analysis
Adolescent / Rwanda / Movement disorders / Humans / Genetic Testing / Female / Spinocerebellar ataxia / Pedigree / Phenotype / Genetic Analysis / Ophthalmoplegia / Female / Spinocerebellar ataxia / Pedigree / Phenotype / Genetic Analysis / Ophthalmoplegia
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