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A comparison of nine scales to detect depression in Parkinson disease: which scale to use?

Neurology, 2012-03, Vol.78 (13), p.998-1006

2012

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The association of CAG repeat length with clinical progression in Huntington disease

Neurology, 2006-04, Vol.66 (7), p.1016-1020

2006

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Quantitative Susceptibility Mapping Suggests Altered Brain Iron in Premanifest Huntington Disease

American journal of neuroradiology : AJNR, 2016-05, Vol.37 (5), p.789-796

2016

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The clinical and genetic spectrum of spinocerebellar ataxia 14

Neurology, 2005-04, Vol.64 (7), p.1258-1260

2005

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Huntington's disease--like 2 can present as chorea-acanthocytosis

Neurology, 2003-10, Vol.61 (7), p.1002-1004

2003

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SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion

Neurology, 2001-02, Vol.56 (3), p.299-303

2001

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CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients

Neurology, 2002-03, Vol.58 (6), p.965-967

2002

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Huntington's disease gene (IT15) is widely expressed in human and rat tissues

Neuron (Cambridge, Mass.), 1993-11, Vol.11 (5), p.985-993

1993

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Psychopathology in Patients With Degenerative Cerebellar Diseases: A Comparison to Huntington's Disease

The American journal of psychiatry, 2002-08, Vol.159 (8), p.1306-1314

2002

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A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion

Annals of neurology, 2001-09, Vol.50 (3), p.373-380

2001

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Tubulin detyrosination is a frequent occurrence in breast cancers of poor prognosis

Cancer research (Chicago, Ill.), 2001-07, Vol.61 (13), p.5024-5027

2001

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SCA12: An unusual mutation leads to an unusual spinocerebellar ataxia

Brain research bulletin, 2001-10, Vol.56 (3-4), p.397-403

2001

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Two Novel Single–Base-Pair Substitutions Adjacent to the CAG Repeat in the Huntington Disease Gene (IT15): Implications for Diagnostic Testing

American journal of human genetics, 1999, Vol.64 (1), p.323-325

1999

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A Comparison of Huntington Disease and Huntington Disease-Like 2 Neuropathology

Journal of neuropathology and experimental neurology, 2008-04, Vol.67 (4), p.366-374

2008

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Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus

Archives of neurology (Chicago), 2002-04, Vol.59 (4), p.623

2002

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Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

Nature genetics, 1999-12, Vol.23 (4), p.391-392

1999

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Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2015-10, Vol.168B (7), p.573-585

2015

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Nonpsychiatrist house staff frequently misdiagnose psychiatric disorders in general hospital inpatients

Psychosomatics (Washington, D.C.), 1994-09, Vol.35 (5), p.485-491

MARGOLIS, R. L

1994

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SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family

Annals of neurology, 2001-01, Vol.49 (1), p.117-121

2001

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Functional brain changes in presymptomatic Huntington's disease

Annals of neurology, 2004-06, Vol.55 (6), p.879-883

2004

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Huntington's disease-like 2 (HDL2) in North America and Japan

Annals of neurology, 2004-11, Vol.56 (5), p.670-674

2004

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Phenotypic features of Huntington's disease-like 2

Movement disorders, 2003-12, Vol.18 (12), p.1527-1530

2003

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Predictors of neuropathological severity in 100 patients with Huntington's disease

Annals of neurology, 2003-10, Vol.54 (4), p.488-493

2003

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FXTAS, SCA10, and SCA17 in American patients with movement disorders

American journal of medical genetics. Part A, 2005-07, Vol.136A (1), p.87-89

2005

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Clinical signs and symptoms in a large hereditary spastic paraparesis pedigree with a novel spastin mutation

Movement disorders, 2004-06, Vol.19 (6), p.641-648

2004

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A comparison of nine scales to detect depression in Parkinson disease: which scale to use?

The association of CAG repeat length with clinical progression in Huntington disease

Quantitative Susceptibility Mapping Suggests Altered Brain Iron in Premanifest Huntington Disease

The clinical and genetic spectrum of spinocerebellar ataxia 14

Huntington's disease--like 2 can present as chorea-acanthocytosis

SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion

CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients

Huntington's disease gene (IT15) is widely expressed in human and rat tissues

Psychopathology in Patients With Degenerative Cerebellar Diseases: A Comparison to Huntington's Disease

A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion

Tubulin detyrosination is a frequent occurrence in breast cancers of poor prognosis

SCA12: An unusual mutation leads to an unusual spinocerebellar ataxia

Two Novel Single–Base-Pair Substitutions Adjacent to the CAG Repeat in the Huntington Disease Gene (IT15): Implications for Diagnostic Testing

A Comparison of Huntington Disease and Huntington Disease-Like 2 Neuropathology

Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus

Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype

Nonpsychiatrist house staff frequently misdiagnose psychiatric disorders in general hospital inpatients

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family

Functional brain changes in presymptomatic Huntington's disease

Huntington's disease-like 2 (HDL2) in North America and Japan

Phenotypic features of Huntington's disease-like 2

Predictors of neuropathological severity in 100 patients with Huntington's disease

FXTAS, SCA10, and SCA17 in American patients with movement disorders

Clinical signs and symptoms in a large hereditary spastic paraparesis pedigree with a novel spastin mutation

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