Cargando…

Religiosity in patients with amyotrophic lateral sclerosis, a cross-country comparison

PURPOSE: Amyotrophic lateral sclerosis (ALS) is a progressive motor impairment leading to early death. Religiousness is one of the factors potentially alleviating the psychological burden of patients. However, its role might vary according to cultural context. Our study aimed to analyze religiosity,...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ciećwierska, Katarzyna, Lulé, Dorothée, Helczyk, Olga, Nieporęcki, Krzysztof, Bielecki, Maksymilian, Baader, Susanne, Ludolph, Albert C., Kuźma-Kozakiewicz, Magdalena
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer International Publishing 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328897/ https://www.ncbi.nlm.nih.gov/pubmed/36929475 http://dx.doi.org/10.1007/s11136-023-03383-4

Ejemplares similares

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

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

An observational study on quality of life and preferences to sustain life in locked-in state
por: Kuzma-Kozakiewicz, Magdalena, 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)

Saccadic intrusions in amyotrophic lateral sclerosis (ALS)
por: Becker, Wolfgang, et al.
Publicado: (2019)

Ethical Principles in Patient-Centered Medical Care to Support Quality of Life in Amyotrophic Lateral Sclerosis
por: Lulé, Dorothée, et al.
Publicado: (2019)

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

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

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

Neuropsychological deficits have only limited impact on psychological well-being in amyotrophic lateral sclerosis
por: Schrempf, Till, et al.
Publicado: (2021)

Multimodal in vivo staging in amyotrophic lateral sclerosis using artificial intelligence
por: Behler, Anna, et al.
Publicado: (2022)

Longitudinal monitoring of amyotrophic lateral sclerosis by diffusion tensor imaging: Power calculations for group studies
por: Behler, Anna, et al.
Publicado: (2022)

Existential decision-making in a fatal progressive disease: how much do legal and medical frameworks matter?
por: Weber, Christian, et al.
Publicado: (2017)

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

A multivariate Bayesian classification algorithm for cerebral stage prediction by diffusion tensor imaging in amyotrophic lateral sclerosis
por: Behler, Anna, et al.
Publicado: (2022)

Functional connectivity changes resemble patterns of pTDP-43 pathology in amyotrophic lateral sclerosis
por: Schulthess, Ines, et al.
Publicado: (2016)

Imaging the pathoanatomy of amyotrophic lateral sclerosis in vivo: targeting a propagation-based biological marker
por: Kassubek, Jan, et al.
Publicado: (2018)

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

Perception of Emotional Facial Expressions in Amyotrophic Lateral Sclerosis (ALS) at Behavioural and Brain Metabolic Level
por: Aho-Özhan, Helena E. A., et al.
Publicado: (2016)

Potential Preventive Strategies for Amyotrophic Lateral Sclerosis
por: Kuraszkiewicz, B., et al.
Publicado: (2020)

Cognitive Performance of Patients with Adult 5q-Spinal Muscular Atrophy and with Amyotrophic Lateral Sclerosis
por: Osmanovic, Alma, et al.
Publicado: (2020)

The use of P300-based BCIs in amyotrophic lateral sclerosis: from augmentative and alternative communication to cognitive assessment
por: Cipresso, Pietro, et al.
Publicado: (2012)

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)

Non-invasive ventilation in amyotrophic lateral sclerosis
por: Dorst, Johannes, et al.
Publicado: (2019)

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)

Eye Movement Deficits Are Consistent with a Staging Model of pTDP-43 Pathology in Amyotrophic Lateral Sclerosis
por: Gorges, Martin, et al.
Publicado: (2015)

Disease-modifying and symptomatic treatment of amyotrophic lateral sclerosis
por: Dorst, Johannes, et al.
Publicado: (2017)

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

The Fragile X Protein Family in Amyotrophic Lateral Sclerosis
por: Mueller, Sarah, et al.
Publicado: (2023)

Synapse loss in the prefrontal cortex is associated with cognitive decline in amyotrophic lateral sclerosis
por: Henstridge, Christopher M., et al.
Publicado: (2017)

ROCK-ALS: Protocol for a Randomized, Placebo-Controlled, Double-Blind Phase IIa Trial of Safety, Tolerability and Efficacy of the Rho Kinase (ROCK) Inhibitor Fasudil in Amyotrophic Lateral Sclerosis
por: Lingor, Paul, et al.
Publicado: (2019)

Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations
por: Wiesenfarth, Maximilian, et al.
Publicado: (2023)

Adipose Tissue Distribution Predicts Survival in Amyotrophic Lateral Sclerosis
por: Lindauer, Eva, et al.
Publicado: (2013)

Amyotrophic lateral sclerosis
por: Wijesekera, Lokesh C, et al.
Publicado: (2009)

Current knowledge and recent insights into the genetic basis of amyotrophic lateral sclerosis
por: Volk, Alexander E., et al.
Publicado: (2018)

Pharyngeal electrical stimulation in amyotrophic lateral sclerosis: a pilot study
por: Herrmann, Christine, et al.
Publicado: (2022)

Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis
por: Freischmidt, Axel, et al.
Publicado: (2013)

Diffusion Tensor Imaging in Amyotrophic Lateral Sclerosis: Machine Learning for Biomarker Development
por: Behler, Anna, et al.
Publicado: (2023)

Well-being in amyotrophic lateral sclerosis: a pilot experience sampling study
por: Real, Ruben G. L., et al.
Publicado: (2014)

Intraspinal Transplantation of the Adipose Tissue-Derived Regenerative Cells in Amyotrophic Lateral Sclerosis in Accordance with the Current Experts' Recommendations: Choosing Optimal Monitoring Tools
por: Kuzma-Kozakiewicz, Magdalena, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_pmvn0ln44ecej8fie9sgbmf096