Variation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis

B Marin, F Boumédiene, G Logroscino… - International journal …, 2017 - academic.oup.com
Background To assess the worldwide variation of amyotrophic lateral sclerosis (ALS)
incidence, we performed a systematic review and meta-analysis of population-based data …

Amyotrophic lateral sclerosis

O Hardiman, A Al-Chalabi, A Chio, EM Corr… - Nature reviews Disease …, 2017 - nature.com
Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease, is characterized
by the degeneration of both upper and lower motor neurons, which leads to muscle …

The Rotterdam Study: 2018 update on objectives, design and main results

MA Ikram, GGO Brusselle, SD Murad… - European journal of …, 2017 - Springer
Abstract The Rotterdam Study is a prospective cohort study ongoing since 1990 in the city of
Rotterdam in The Netherlands. The study targets cardiovascular, endocrine, hepatic …

Projected increase in amyotrophic lateral sclerosis from 2015 to 2040

KC Arthur, A Calvo, TR Price, JT Geiger, A Chio… - Nature …, 2016 - nature.com
Although amyotrophic lateral sclerosis (ALS) is relatively rare, the socioeconomic
significance of the disease is extensive. It is therefore vital to project the epidemiologic trend …

Global, regional, and national burden of motor neuron diseases 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016

G Logroscino, M Piccininni, B Marin, E Nichols… - The Lancet …, 2018 - thelancet.com
Background Understanding how prevalence, incidence, and mortality of motor neuron
diseases change over time and by location is crucial for understanding the causes of these …

The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration

S Opie-Martin, A Iacoangeli, SD Topp, O Abel… - Nature …, 2022 - nature.com
Superoxide dismutase (SOD1) gene variants may cause amyotrophic lateral sclerosis, some
of which are associated with a distinct phenotype. Most studies assess limited variants or …

Amyotrophic lateral sclerosis descriptive epidemiology: the origin of geographic difference

G Logroscino, M Piccininni - Neuroepidemiology, 2019 - karger.com
Amyotrophic lateral sclerosis (ALS) epidemiology has rapidly developed in the last 30 years
alongside the evolving changes in concepts in the field of clinical ALS and also due to the …

Sex and gender differences in Alzheimer's disease, Parkinson's disease, and Amyotrophic Lateral Sclerosis: A narrative review

A Nicoletti, R Baschi, CE Cicero, S Iacono… - Mechanisms of ageing …, 2023 - Elsevier
Abstract Neurodegenerative diseases (NDs), including Alzheimer's disease (AD),
Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS), exhibit high phenotypic …

The changing picture of amyotrophic lateral sclerosis: lessons from European registers

O Hardiman, A Al-Chalabi, C Brayne… - Journal of Neurology …, 2017 - jnnp.bmj.com
Prospective population based-registers of amyotrophic lateral sclerosis (ALS) have operated
in Europe for over two decades, and have provided important insights into our …

The global burden of motor neuron disease: an analysis of the 2019 global burden of disease study

J Park, JE Kim, TJ Song - Frontiers in Neurology, 2022 - frontiersin.org
Up-to-date, accurate information on the disease burden of motor neuron disease (MND) is
the cornerstone for evidence-based resource allocation and healthcare planning. We aimed …