The epidemiology of ALS: a conspiracy of genes, environment and time

Lifetime physical activity and the risk of amyotrophic lateral sclerosis

(2013) M. H. B. Huisman et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Changes in cognition and behaviour in amyotrophic lateral sclerosis: nature of impairment and implications for assessment

(2013) Laura H Goldstein et al.   LANCET NEUROLOGY

Prediagnostic body fat and risk of death from amyotrophic lateral sclerosis: The EPIC cohort

(2013) V. Gallo et al.   NEUROLOGY

Cognitive changes predict functional decline in ALS: A population-based longitudinal study

(2013) M. Elamin et al.   NEUROLOGY

Amyotrophic lateral sclerosis/motor neuron disease deaths in the United States, 1999–2009

(2013) Jason M. Mehal et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Incidence of Amyotrophic Lateral Sclerosis Among American Indians and Alaska Natives

(2013) Paul H. Gordon et al.   JAMA Neurology

Smoking, Alcohol Consumption, and the Risk of Amyotrophic Lateral Sclerosis: A Population-based Study

(2012) S. W. de Jong et al.   AMERICAN JOURNAL OF EPIDEMIOLOGY

C9ORF72 Repeat Expansion in Amyotrophic Lateral Sclerosis in the Kii Peninsula of Japan

(2012) Hiroyuki Ishiura et al.   ARCHIVES OF NEUROLOGY

A proposed staging system for amyotrophic lateral sclerosis

(2012) J. C. Roche et al.   BRAIN

How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia

(2012) Marka van Blitterswijk et al.   CURRENT OPINION IN NEUROLOGY

The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder

(2012) Bradley N Smith et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Analysis of theC9orf72Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide

(2012) Alberto García-Redondo et al.   HUMAN MUTATION

ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics

(2012) Olubunmi Abel et al.   HUMAN MUTATION

Riluzole and Prognostic Factors in Amyotrophic Lateral Sclerosis Long-term and Short-term Survival: A Population-Based Study of 1149 Cases in Taiwan

(2012) Charles Tzu-Chi Lee et al.   JOURNAL OF EPIDEMIOLOGY

Amyotrophic lateral sclerosis in Sardinia, insular Italy, 1995–2009

(2012) Maura Pugliatti et al.   JOURNAL OF NEUROLOGY

Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72

(2012) T. Konno et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study

(2012) Susan Byrne et al.   LANCET NEUROLOGY

A hexanucleotide repeat expansion in C9ORF72 causes familial and sporadic ALS in Taiwan

(2012) Ching-Paio Tsai et al.   NEUROBIOLOGY OF AGING

Analysis of the C9orf72 hexanucleotide repeat expansion in Korean patients with familial and sporadic amyotrophic lateral sclerosis

(2012) Ja-Hyun Jang et al.   NEUROBIOLOGY OF AGING

Utility of Capture-Recapture Methodology to Assess Completeness of Amyotrophic Lateral Sclerosis Case Ascertainment

(2012) Michael Wittie et al.   NEUROEPIDEMIOLOGY

Amyotrophic lateral sclerosis in Piedmont (Italy): A Bayesian spatial analysis of the incident cases

(2012) Giuseppe Migliaretti et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Premorbid body mass index and risk of amyotrophic lateral sclerosis

(2012) Éilis J. O'Reilly et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS

(2011) Safa Al-Sarraj et al.   ACTA NEUROPATHOLOGICA

Increase in motor neuron disease mortality in Spain: Temporal and geographical analysis (1990–2005)

(2011) Veronica Alonso et al.   Amyotrophic Lateral Sclerosis

Proposed criteria for familial amyotrophic lateral sclerosis

(2011) Susan Byrne et al.   Amyotrophic Lateral Sclerosis

Smoking and Risk of Amyotrophic Lateral Sclerosis

(2011) Hao Wang et al.   ARCHIVES OF NEUROLOGY

Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP Gene

(2011) Adriano Chiò   ARCHIVES OF NEUROLOGY

The risk to relatives of patients with sporadic amyotrophic lateral sclerosis

(2011) M. F. Hanby et al.   BRAIN

Modelling the Effects of Penetrance and Family Size on Rates of Sporadic and Familial Disease

(2011) Ammar Al-Chalabi et al.   HUMAN HEREDITY

Beneficial vascular risk profile is associated with amyotrophic lateral sclerosis

(2011) N. A. Sutedja et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study

(2011) Julie Phukan et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Population based epidemiology of amyotrophic lateral sclerosis using capture-recapture methodology

(2011) M. H. B. Huisman et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Contribution of geolocalisation to neuroepidemiological studies: Incidence of ALS and environmental factors in Limousin, France

(2011) Farid Boumédiène et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Clinical genetics of amyotrophic lateral sclerosis: what do we really know?

(2011) Peter M. Andersen et al.   Nature Reviews Neurology

The epidemiology of motor neuron disease in Northern Ireland using capture-recapture methodology

(2010) Colette Donaghy et al.   Amyotrophic Lateral Sclerosis

The sex ratio in amyotrophic lateral sclerosis: A population based study

(2010) Zita R. Manjaly et al.   Amyotrophic Lateral Sclerosis

Association of smoking with amyotrophic lateral sclerosis risk and survival in men and women: a prospective study

(2010) Alvaro Alonso et al.   BMC Neurology

Validation of the historical adulthood physical activity questionnaire (HAPAQ) against objective measurements of physical activity

(2010) Hervé Besson et al.   International Journal of Behavioral Nutrition and Physical Activity

Concordance between site of onset and limb dominance in amyotrophic lateral sclerosis

(2010) M. R. Turner et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

An estimate of amyotrophic lateral sclerosis heritability using twin data

(2010) A. Al-Chalabi et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Metastatic choriocarcinoma

(2010) U. Vivekananda et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis

(2010) S. Byrne et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Temporal trends and geographic clusters of mortality from amyotrophic lateral sclerosis in Japan, 1995–2004

(2010) Yuriko Doi et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Neurological mortality among U.S. veterans of the Persian Gulf War: 13-year follow-up

(2009) Shannon K. Barth et al.   AMERICAN JOURNAL OF INDUSTRIAL MEDICINE

Prognosis of ALS: Comparing data from the Limousin referral centre, France, and a Uruguayan population

(2009) Juan Gil et al.   Amyotrophic Lateral Sclerosis

Exposure to chemicals and metals and risk of amyotrophic lateral sclerosis: A systematic review

(2009) Nadia A. Sutedja et al.   Amyotrophic Lateral Sclerosis

What we truly know about occupation as a risk factor for ALS: A critical and systematic review

(2009) Nadia A. Sutedja et al.   Amyotrophic Lateral Sclerosis

Prognostic factors in ALS: A critical review

(2009) Adriano Chiò et al.   Amyotrophic Lateral Sclerosis

Beyond Guam: The cyanobacteria/BMAA hypothesis of the cause of ALS and other neurodegenerative diseases

(2009) Walter G. Bradley et al.   Amyotrophic Lateral Sclerosis

A Long-term Prospective Study of the Natural Course of Sporadic Adult-Onset Lower Motor Neuron Syndromes

(2009) Renske M. Van den Berg-Vos et al.   ARCHIVES OF NEUROLOGY

Incidence of amyotrophic lateral sclerosis in Europe

(2009) G. Logroscino et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Study of 962 patients indicates progressive muscular atrophy is a form of ALS

(2009) W. -K. Kim et al.   NEUROLOGY

Epidemiology of ALS in Italy: A 10-year prospective population-based study

(2009) A. Chio et al.   NEUROLOGY

Reduced frequency of ALS in an ethnically mixed population: A population-based mortality study

(2009) T. Zaldivar et al.   NEUROLOGY

Natural history and clinical features of the flail arm and flail leg ALS variants

(2009) L. C. Wijesekera et al.   NEUROLOGY

Smoking may be considered an established risk factor for sporadic ALS

(2009) C. Armon   NEUROLOGY

Latent Cluster Analysis of ALS Phenotypes Identifies Prognostically Differing Groups

(2009) Jeban Ganesalingam et al.   PLoS One

Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6

(2009) C. Vance et al.   SCIENCE

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

(2009) T. J. Kwiatkowski et al.   SCIENCE

An all-Ireland epidemiological study of MND, 2004-2005

(2008) C. Donaghy et al.   EUROPEAN JOURNAL OF NEUROLOGY

Clinical characteristics and survival pattern of 1153 patients with amyotrophic lateral sclerosis: Experience over 30 years from India

(2008) A. Nalini et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Geographical Clustering of Amyotrophic Lateral Sclerosis in South-East England: A Population Study

(2008) Kirsten M. Scott et al.   NEUROEPIDEMIOLOGY

The ALS/PDC syndrome of Guam and the cycad hypothesis

(2008) J. C. Steele et al.   NEUROLOGY

An epidemiologic investigation of amyotrophic lateral sclerosis in Jefferson County, Missouri, 1998–2002

(2007) George Turabelidze et al.   NEUROTOXICOLOGY