The challenge of amyotrophic lateral sclerosis descriptive epidemiology: to estimate low incidence rates across complex phenotypes in different geographic areas

G Logroscino, D Urso, R Tortelli - Current Opinion in Neurology, 2022 - journals.lww.com
Population-based disease registries have played a major role in developing new knowledge
on ALS, in characterizing genotype-phenotype correlations, in discovering new genetic …

Three different short-interval intracortical inhibition methods in early diagnosis of amyotrophic lateral sclerosis

H Tankisi, H Pia, K Strunge, J Howells… - … Lateral Sclerosis and …, 2023 - Taylor & Francis
Objectives: To compare the utility of conventional amplitude measurements of short-interval
intracortical inhibition (A-SICI) with two threshold-tracking (T-SICI) methods, as aids to early …

LAENALS: epidemiological and clinical features of amyotrophic lateral sclerosis in Latin America

B Vélez-GóMEZ, A Perna, C Vazquez… - … Lateral Sclerosis and …, 2024 - Taylor & Francis
Abstract Objective The Latin American Epidemiologic study of ALS (LAENALS) aims to
gather data on ALS epidemiology, phenotype, and risk factors in Cuba, Chile, and Uruguay …

Geographical distribution of clinical trials in amyotrophic lateral sclerosis: a scoping review

B García-Parra, JM Guiu, M Povedano… - … Lateral Sclerosis and …, 2024 - Taylor & Francis
Introduction: Clinical trials location is determined by many factors, including the availability
of patient populations, regulatory environment, scientific expertise, and cost considerations …

Incidence of amyotrophic lateral sclerosis in Chile

P Lillo, P Zitko, G Godoy-Reyes, G Asenjo… - … Lateral Sclerosis and …, 2024 - Taylor & Francis
Objective This study aimed to estimate amyotrophic lateral sclerosis (ALS) incidence and
survival rates in the Metropolitan region of Chile. Methods We conducted a cohort study of …

Amyotrophic Lateral Sclerosis in Latin America: Epidemiology, clinical features and clinical practices on the diagnosis and management of ALS among neurologists

DAE Aleman - 2022 - theses.hal.science
Amyotrophic Lateral sclerosis is a neurodegenerative disease with a poor survival. ALS
heterogeneity has been observed among epidemiological indicators and clinical …

[HTML][HTML] TARDBP-related amyotrophic lateral sclerosis-frontotemporal dementia

V Manohar, L Crowley, J Sreedharan - 2015 - europepmc.org
In this GeneReview, TARDBP amyotrophic lateral sclerosis-frontotemporal dementia
(TARDBP-ALS-FTD) refers to the spectrum of phenotypes caused by pathogenic variants in …

[HTML][HTML] TARDBP-Related Amyotrophic Lateral Sclerosis-Frontotemporal Dementia Synonyms: TARDBP-ALS-FTD, TDP-43 Proteinopathy, TDP-43-Linked ALS-FTD

V Manohar, J Sreedharan - europepmc.org
In this GeneReview, TARDBP amyotrophic lateral sclerosis-frontotemporal dementia
(TARDBP-ALS-FTD) refers to the spectrum of phenotypes caused by pathogenic variants in …

[引用][C] Detección, cuantificación y análisis de oxilipinas en pacientes con Esclerosis Lateral Amiotrófica

M Mastrogiovanni - 2022 - Udelar. FC.