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Spinocerebellar Ataxias in Brazil—Frequencies and Modulating Effects of Related Genes

(2013) Raphael Machado de Castilhos et al.   CEREBELLUM

The Cuban program for predictive testing of SCA2: 11 years and 768 individuals to learn from

(2013) T Cruz-Mariño et al.   CLINICAL GENETICS

What Counts as Effective Genetic Counselling for Presymptomatic Testing in Late-Onset Disorders? A Study of the Consultand’s Perspective

(2013) Lídia Guimarães et al.   Journal of Genetic Counseling

Hereditary Ataxia and Spastic Paraplegia in Portugal

(2013) Paula Coutinho et al.   JAMA Neurology

Recommendations for the predictive genetic test in Huntington's disease

(2012) R MacLeod et al.   CLINICAL GENETICS

The Challenges of Incorporating Genetic Testing in the Unified National Health System in Brazil

(2012) Débora Gusmão Melo et al.   Genetic Testing and Molecular Biomarkers

Psychological Well-Being and Family Satisfaction Levels Five Years After Being Confirmed as a Carrier of the Machado-Joseph Disease Mutation

(2012) Carlos Gonzalez et al.   Genetic Testing and Molecular Biomarkers

Presymptomatic Testing for Neurogenetic Diseases in Brazil: Assessing Who Seeks and Who Follows through with Testing

(2011) Caroline Santa Maria Rodrigues et al.   Journal of Genetic Counseling

Toward understanding Machado–Joseph disease

(2011) Maria do Carmo Costa et al.   PROGRESS IN NEUROBIOLOGY

EMQN Best Practice Guidelines for molecular genetic testing of SCAs

(2010) Jorge Sequeiros et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Role of the Disease in the Psychological Impact of Pre-Symptomatic Testing for SCA2 and FAP ATTRV30M: Experience with the Disease, Kinship and Gender of the Transmitting Parent

(2009) Milena Paneque et al.   Journal of Genetic Counseling

Experience and outcome of 3 years of a European EQA scheme for genetic testing of the spinocerebellar ataxias

(2008) Sara Seneca et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Decreasing uptake of predictive testing for Huntington's disease in a German centre: 12 years' experience (1993–2004)

(2008) Christiane Bernhardt et al.   EUROPEAN JOURNAL OF HUMAN GENETICS