Late-onset Huntington’s disease with 40–42 CAG expansion

Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis

(2018) Caterina Fusilli et al.   LANCET NEUROLOGY

Clinical and genetic characteristics of late-onset Huntington's disease

(2018) Mayke Oosterloo et al.   PARKINSONISM & RELATED DISORDERS

Late-onset Huntington's disease: Diagnostic and prognostic considerations

(2014) Georgios Koutsis et al.   PARKINSONISM & RELATED DISORDERS

Caudate glucose hypometabolism in a subject carrying an unstable allele of intermediate CAG33 repeat length in the Huntington's disease gene

(2011) Ferdinando Squitieri et al.   MOVEMENT DISORDERS

Huntington's disease: from molecular pathogenesis to clinical treatment

(2010) Christopher A Ross et al.   LANCET NEUROLOGY

Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis

(2010) Sarah J Tabrizi et al.   LANCET NEUROLOGY

Late onset Huntington Disease: Clinical and genetic characteristics of 34 cases

(2008) Hillary Lipe et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Huntington's disease as caused by 34 CAG repeats

(2008) Jürgen Andrich et al.   MOVEMENT DISORDERS