Ataxia

Ataxia telangiectasia and Nijmegen breakage syndrome : neurological, immunological and genetic aspects / Johannes Alphonsus Paulina Hielschema:ProductModel Ataxic disorders / vol. ed. Sankara H. Subramony and Alexandra Dürrschema:ProductModel Autosomal dominant cerebellar ataxias : clinical and genetic studies in Dutch patients / Bart Petrus Christoffel van de Warrenburgschema:ProductModel Diversity in functional complementation of the ataxia telangiectasia phenotype in mammalian cells / Willem Jongmansschema:ProductModel DNA synthesis in ataxia telangiectasia / door Nicolaas Gerardus Joseph Jaspersschema:ProductModel DNA synthesis in ataxia telangiectasia / door Nicolaas Gerardus Joseph Jaspersschema:ProductModel Dynamics of ataxin-1 in spinocerebellar ataxia type 1 / Hilde Aagje Gerbrich Krolschema:ProductModel Dynamics of Ataxin-1 in spinocerebellar ataxia type 1 / Hilde Aagje Gerbrich Krolschema:ProductModel Genetic and molecular mechanisms underlying spinocerebellar ataxias / Justyna Jezierskaschema:ProductModel Neurogenerative diseases and the protein quality control system / Kay Seidelschema:ProductModel The localization and identification of novel SCA genes in the Dutch autosomal dominant cerebellar ataxia population / Dineke Suzanne Verbeekschema:ProductModel The molecular neuropathology of spinocerebellar ataxia type 23 / Cleo Josephine Lyzanne Maria Smeetsschema:ProductModel The molecular neuropathology of spinocerebellar ataxia type 23 / Cleo Josephine Lyzanne Maria Smeetsschema:ProductModel The role of heat shock proteins in polyQ disorders / Marianne Petra Zijlstraschema:ProductModel The role of heat shock proteins in polyQ disorders / Marianne Petra Zijlstraschema:ProductModel