Atypical parkinsonism in C9orf72 expansions: a case report and systematic review of 45 cases from the literature

C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis

(2015) Jonathan D Rohrer et al.   LANCET NEUROLOGY

C9ORF72 hexanucleotide repeat expansions are a frequent cause of Huntington disease phenocopies in the Greek population

(2015) Georgios Koutsis et al.   NEUROBIOLOGY OF AGING

The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism

(2015) Lucia V. Schottlaender et al.   NEUROBIOLOGY OF AGING

The Spectrum of C9orf72-mediated Neurodegeneration and Amyotrophic Lateral Sclerosis

(2015) Johnathan Cooper-Knock et al.   Neurotherapeutics

C9ORF72 repeat expansions in mice cause TDP-43 pathology, neuronal loss, and behavioral deficits

(2015) J. Chew et al.   SCIENCE

Clinicopathological Study of Patients With C9ORF72-Associated Frontotemporal Dementia Presenting With Delusions

(2014) Shunichiro Shinagawa et al.   JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY

C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome

(2014) Vladimir S. Kostić et al.   JOURNAL OF NEUROLOGY

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease

(2014) J. Theuns et al.   NEUROLOGY

Efficacy of subthalamic nucleus stimulation in C9ORF72 expansion related parkinsonism

(2014) T. Danaila et al.   PARKINSONISM & RELATED DISORDERS

Multiple System Atrophy and Amyotrophic Lateral Sclerosis in a Family With Hexanucleotide Repeat Expansions inC9orf72

(2014) Jill S. Goldman et al.   JAMA Neurology

Frontotemporal Dementia Associated With theC9ORF72Mutation

(2014) Emma Devenney et al.   JAMA Neurology

C9orf72 repeat expansions are a rare genetic cause of parkinsonism

(2013) Suzanne Lesage et al.   BRAIN

The Addenbrooke's Cognitive Examination for the differential diagnosis and longitudinal assessment of patients with parkinsonian disorders

(2013) T. Rittman et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

C9orf72 repeat expansions are restricted to the ALS-FTD spectrum

(2013) Nicola Ticozzi et al.   NEUROBIOLOGY OF AGING

C9ORF72 expansions, parkinsonism, and Parkinson disease: A clinicopathologic study

(2013) J. Cooper-Knock et al.   NEUROLOGY

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies

(2013) D. J. Hensman Moss et al.   NEUROLOGY

Enlarging the clinical spectrum associated with C9orf 72 repeat expansions: Findings in an Italian cohort of patients with Parkinsonian syndromes and relevance for genetic counselling

(2013) Paola Origone et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72

(2013) David MA Mann et al.   Acta Neuropathologica Communications

Suicide Attempt as the Presenting Symptom ofC9orf72Dementia

(2012) Matthis Synofzik et al.   AMERICAN JOURNAL OF PSYCHIATRY

Characterization of a Family With c9FTD/ALS Associated With the GGGGCC Repeat Expansion in C9ORF72

(2012) Rodolfo Savica et al.   ARCHIVES OF NEUROLOGY

Frontotemporal Dementia in a Brazilian Kindred With the C9orf72 Mutation

(2012) Leonel T. Takada   ARCHIVES OF NEUROLOGY

Investigation of C9orf72 in 4 Neurodegenerative Disorders

(2012) Zhengrui Xi et al.   ARCHIVES OF NEUROLOGY

Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

(2012) G.-Y. R. Hsiung et al.   BRAIN

Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72

(2012) Johnathan Cooper-Knock et al.   BRAIN

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

(2012) J. S. Snowden et al.   BRAIN

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

(2012) Bradley F. Boeve et al.   BRAIN

Corticobasal and ataxia syndromes widen the spectrum ofC9ORF72hexanucleotide expansion disease

(2012) SG Lindquist et al.   CLINICAL GENETICS

Frontotemporal dementia with psychosis, parkinsonism, visuo-spatial dysfunction, upper motor neuron involvement associated to expansion of C9ORF72: a peculiar phenotype?

(2012) Gianluca Floris et al.   JOURNAL OF NEUROLOGY

Psychosis,C9ORF72and dementia with Lewy bodies: Table 1

(2012) Julie S Snowden et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism

(2012) Seán O'Dowd et al.   MOVEMENT DISORDERS

Cognitive and behavioral features of c9FTD/ALS

(2012) Bradley F Boeve et al.   Alzheimers Research & Therapy

Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion

(2012) Marco Luigetti et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72

(2011) Melissa E. Murray et al.   ACTA NEUROPATHOLOGICA

Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS

(2011) Mariely DeJesus-Hernandez et al.   NEURON

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

(2011) Alan E. Renton et al.   NEURON

Neuropsychological and clinical heterogeneity of cognitive impairment and dementia in patients with Parkinson's disease

(2010) Angie A Kehagia et al.   LANCET NEUROLOGY

Differential diagnostic value of eye movement recording in PSP-parkinsonism, Richardson's syndrome, and idiopathic Parkinson's disease

(2009) Elmar H. Pinkhardt et al.   JOURNAL OF NEUROLOGY