Cargando…

Potential Preventive Strategies for Amyotrophic Lateral Sclerosis

It may seem useless to propose preventive measures for a disease without established pathogenesis and successful therapy, such as amyotrophic lateral sclerosis (ALS). However, we will show that ALS shares essential molecular mechanisms with aging and that established anti-aging strategies, such as h...

Descripción completa

Detalles Bibliográficos
Autores principales:	Kuraszkiewicz, B., Goszczyńska, H., Podsiadły-Marczykowska, T., Piotrkiewicz, M., Andersen, P., Gromicho, M., Grosskreutz, J., Kuźma-Kozakiewicz, M., Petri, S., Stubbendorf, B., Szacka, K., Uysal, H., de Carvalho, M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2020
Materias:	Neuroscience
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264408/ https://www.ncbi.nlm.nih.gov/pubmed/32528241 http://dx.doi.org/10.3389/fnins.2020.00428

Ejemplares similares

Are There Modifiable Environmental Factors Related to Amyotrophic Lateral Sclerosis?
por: Kuraszkiewicz, Bozenna, et al.
Publicado: (2018)

Influence of Environment and Lifestyle on Incidence and Progress of Amyotrophic Lateral Sclerosis in A German ALS Population
por: Korner, Sonja, et al.
Publicado: (2019)

Emotional Lability at Disease Onset Is an Independent Prognostic Factor of Faster Disease Progression in Amyotrophic Lateral Sclerosis
por: Barć, Krzysztof, et al.
Publicado: (2020)

Analysis of routine blood parameters in patients with amyotrophic lateral sclerosis and evaluation of a possible correlation with disease progression—a multicenter study
por: Hertel, Nora, et al.
Publicado: (2022)

Trends in the diagnostic delay and pathway for amyotrophic lateral sclerosis patients across different countries
por: Falcão de Campos, Catarina, et al.
Publicado: (2023)

SOD1 mutations associated with amyotrophic lateral sclerosis analysis of variant severity
por: Berdyński, Mariusz, et al.
Publicado: (2022)

Amyotrophic lateral sclerosis: a dying motor unit?
por: Piotrkiewicz, Maria, et al.
Publicado: (2013)

Spreading in ALS: The relative impact of upper and lower motor neuron involvement
por: Gromicho, Marta, et al.
Publicado: (2020)

Does the MUNIX Method Reflect Clinical Dysfunction in Amyotrophic Lateral Sclerosis: A Practical Experience
por: Gawel, Malgorzata, et al.
Publicado: (2016)

Amyotrophic Lateral Sclerosis: Advances and Prospects
por: Boentert, Matthias, et al.
Publicado: (2023)

Validation of qPCR reference genes in lymphocytes from patients with amyotrophic lateral sclerosis
por: Usarek, Ewa, et al.
Publicado: (2017)

Plasma profiling reveals three proteins associated to amyotrophic lateral sclerosis
por: Häggmark, Anna, et al.
Publicado: (2014)

γ' Fibrinogen as a Predictor of Survival in Amyotrophic Lateral Sclerosis
por: Pronto-Laborinho, Ana Catarina, et al.
Publicado: (2021)

Delayed Diagnosis and Diagnostic Pathway of ALS Patients in Portugal: Where Can We Improve?
por: Falcão de Campos, Catarina, et al.
Publicado: (2021)

Quality of life and depression in patients with amyotrophic lateral sclerosis – does the country of origin matter?
por: Ciećwierska, Katarzyna, et al.
Publicado: (2023)

Neuroimaging Endpoints in Amyotrophic Lateral Sclerosis
por: Menke, Ricarda A. L., et al.
Publicado: (2016)

Bilateral changes in afterhyperpolarization duration of spinal motoneurones in post-stroke patients
por: Kuraszkiewicz, Bożenna, et al.
Publicado: (2018)

Cerebrospinal Fluid Chitinases as Biomarkers for Amyotrophic Lateral Sclerosis
por: Costa, Júlia, et al.
Publicado: (2021)

Use of vitamins by participants in amyotrophic lateral sclerosis clinical trials
por: Prell, Tino, et al.
Publicado: (2020)

Corrigendum: γ′ Fibrinogen as a Predictor of Survival in Amyotrophic Lateral Sclerosis
por: Pronto-Laborinho, Ana Catarina, et al.
Publicado: (2021)

Religiosity in patients with amyotrophic lateral sclerosis, a cross-country comparison
por: Ciećwierska, Katarzyna, et al.
Publicado: (2023)

Differential Expression of miRNAs in Amyotrophic Lateral Sclerosis Patients
por: Gomes, Bruno Costa, et al.
Publicado: (2023)

Sporadic Spinal-Onset Amyotrophic Lateral Sclerosis Associated with Myopathy in Three Unrelated Portuguese Patients
por: Oliveira Santos, Miguel, et al.
Publicado: (2023)

Well‐being on supportive techniques in amyotrophic lateral sclerosis: from neurologists' perspective
por: Barć, Krzysztof, et al.
Publicado: (2022)

Longitudinal diffusion tensor imaging in amyotrophic lateral sclerosis
por: Keil, Carsten, et al.
Publicado: (2012)

Amyotrophic Lateral Sclerosis and Novel Therapeutic Strategies
por: Morrison, Brett, et al.
Publicado: (2012)

Triclustering-based classification of longitudinal data for prognostic prediction: targeting relevant clinical endpoints in amyotrophic lateral sclerosis
por: Soares, Diogo F., et al.
Publicado: (2023)

The Chitinases as Biomarkers for Amyotrophic Lateral Sclerosis: Signals From the CNS and Beyond
por: Gaur, Nayana, et al.
Publicado: (2020)

Widespread sensorimotor and frontal cortical atrophy in Amyotrophic Lateral Sclerosis
por: Grosskreutz, Julian, et al.
Publicado: (2006)

Classification of amyotrophic lateral sclerosis by brain volume, connectivity, and network dynamics
por: Thome, Janine, et al.
Publicado: (2021)

Cerebrospinal fluid biomarkers of disease activity and progression in amyotrophic lateral sclerosis
por: Dreger, Marie, et al.
Publicado: (2022)

A Case Report of Amyotrophic Lateral Sclerosis in a Patient With Klippel–Feil Syndrome—a Familial Occurrence: A Potential Role of TGF-β Signaling Pathway
por: Jamrozik, Zygmunt, et al.
Publicado: (2015)

Poor emotional well-being is associated with rapid progression in amyotrophic lateral sclerosis
por: Prell, Tino, et al.
Publicado: (2019)

Afterhyperpolarization of human motoneurons firing double and triple discharges
por: Piotrkiewicz, Maria, et al.
Publicado: (2014)

Blood–Brain Barrier Disruption Is Not Associated With Disease Aggressiveness in Amyotrophic Lateral Sclerosis
por: Prell, Tino, et al.
Publicado: (2021)

Magnetic Resonance Imaging in Amyotrophic Lateral Sclerosis
por: Kollewe, Katja, et al.
Publicado: (2012)

The ER mitochondria calcium cycle and ER stress response as therapeutic targets in amyotrophic lateral sclerosis
por: Tadic, Vedrana, et al.
Publicado: (2014)

Extent of cortical involvement in amyotrophic lateral sclerosis – an analysis based on cortical thickness
por: Thorns, Johannes, et al.
Publicado: (2013)

Skeletal muscle in amyotrophic lateral sclerosis
por: Shefner, Jeremy M, et al.
Publicado: (2023)

Pathologic expansion in the C9orf72 gene is associated with accelerated decline of respiratory function and decreased survival in amyotrophic lateral sclerosis
por: Miltenberger-Miltenyi, Gabriel, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_s3o7ef6u62b7d7gog587gbkqh9