Cargando…

Enteral feeding is associated with longer survival in the advanced stages of prion disease

To report the frequency, complications, survival and motivations for enteral feeding in UK patients with prion diseases. We analysed data from an ongoing prospective observational cohort study of UK patients with prion diseases (n = 635). Gastrostomy-treated cases were matched by age, gender, diseas...

Descripción completa

Detalles Bibliográficos
Autores principales:	McNiven, Kirsty, Nihat, Akin, Mok, Tze How, Tesfamichael, Selam, O’Donnell, Veronica, Rudge, Peter, Collinge, John, Mead, Simon
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2019
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425295/ https://www.ncbi.nlm.nih.gov/pubmed/32954259 http://dx.doi.org/10.1093/braincomms/fcz012

Ejemplares similares

Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease
por: Nihat, Akin, et al.
Publicado: (2022)

Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease
por: Nihat, Akın, et al.
Publicado: (2022)

Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases
por: Mok, Tze How, et al.
Publicado: (2021)

Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort Study
por: Sequeira, Danielle, et al.
Publicado: (2022)

Assessing initial MRI reports for suspected CJD patients
por: Jesuthasan, Aaron, et al.
Publicado: (2022)

The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical feature
por: Caine, Diana, et al.
Publicado: (2018)

Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseases
por: Thompson, Andrew G. B., et al.
Publicado: (2021)

Detection of Creutzfeldt-Jakob disease prions in skin: implications for healthcare
por: Nihat, Akin, et al.
Publicado: (2018)

NT1-Tau Is Increased in CSF and Plasma of CJD Patients, and Correlates with Disease Progression
por: Mengel, David, et al.
Publicado: (2021)

Prion disease diagnosis using subject-specific imaging biomarkers within a multi-kernel Gaussian process
por: Canas, Liane S., et al.
Publicado: (2019)

Estimation of the number of inherited prion disease mutation carriers in the UK
por: Corbie, Rosie, et al.
Publicado: (2022)

Tau, prions and Aβ: the triad of neurodegeneration
por: Reiniger, Lilla, et al.
Publicado: (2010)

Genetics of prion diseases
por: Lloyd, Sarah E, et al.
Publicado: (2013)

Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease
por: Rudge, Peter, et al.
Publicado: (2019)

Evaluating the causality of novel sequence variants in the prion protein gene by example
por: Mok, Tze How, et al.
Publicado: (2018)

Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion disease
por: Mok, Tze How, et al.
Publicado: (2023)

Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases
por: Reiniger, Lilla, et al.
Publicado: (2013)

Quantitative EEG parameters correlate with the progression of human prion diseases
por: Franko, Edit, et al.
Publicado: (2016)

A novel prion protein variant in a patient with semantic dementia
por: Kenny, Joanna, et al.
Publicado: (2017)

Genome-wide association study of behavioural and psychiatric features in human prion disease
por: Thompson, A G B, et al.
Publicado: (2015)

Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS
por: Asante, Emmanuel A., et al.
Publicado: (2020)

Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1
por: Carswell, Christopher, et al.
Publicado: (2012)

The cognitive profile of prion disease: a prospective clinical and imaging study
por: Caine, Diana, et al.
Publicado: (2015)

Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion
por: Brennecke, Nicholas, et al.
Publicado: (2021)

A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis
por: Norsworthy, Penny J., et al.
Publicado: (2020)

Duration of Prion Disease is Longer in Japan Than in Other Countries
por: Nagoshi, Kiwamu, et al.
Publicado: (2011)

Neuroanatomical correlates of prion disease progression - a 3T longitudinal voxel-based morphometry study
por: De Vita, Enrico, et al.
Publicado: (2016)

Safety and efficacy of quinacrine in human prion disease (PRION-1 study): a patient-preference trial
por: Collinge, John, et al.
Publicado: (2009)

Prion protein gene mutation detection using long-read Nanopore sequencing
por: Kroll, François, et al.
Publicado: (2022)

Molecular pathology of human prion disease
por: Wadsworth, Jonathan D. F., et al.
Publicado: (2010)

Plasmacytoid Dendritic Cells Sequester High Prion Titres at Early Stages of Prion Infection
por: Castro-Seoane, Rocio, et al.
Publicado: (2012)

Neuronal antibodies in patients with suspected or confirmed sporadic Creutzfeldt-Jakob disease
por: Rossi, Meghan, et al.
Publicado: (2015)

Imaging and CSF analyses effectively distinguish CJD from its mimics
por: Rudge, Peter, et al.
Publicado: (2018)

Putaminal diffusion tensor imaging measures predict disease severity across human prion diseases
por: Hyare, Harpreet, et al.
Publicado: (2020)

A naturally occurring variant of the human prion protein completely prevents prion disease
por: Asante, Emmanuel A., et al.
Publicado: (2015)

In vitro screen of prion disease susceptibility genes using the scrapie cell assay
por: Brown, Craig A., et al.
Publicado: (2014)

HECTD2 Is Associated with Susceptibility to Mouse and Human Prion Disease
por: Lloyd, Sarah E., et al.
Publicado: (2009)

Spina Bifida Cured by Structure of Iodine and Glycerine
por: McNiven, P. Campbell
Publicado: (1886)

Shadoo (Sprn) and prion disease incubation time in mice
por: Lloyd, Sarah E., et al.
Publicado: (2009)

Unsettling experiences: A qualitative inquiry into young peoples’ narratives of diagnosis for common skin conditions in the United Kingdom
por: McNiven, Abigail, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_rfpgnl6hjd5f9qosb50mdb4vno