Good practice in the management of amyotrophic lateral sclerosis: Clinical guidelines. An evidence‐based review with good practice points. EALSC Working Group

PM Andersen, GD Borasio, R Dengler… - Amyotrophic lateral …, 2007 - Taylor & Francis
The evidence base for diagnosis and management of ALS is still weak, and curative therapy
is lacking. Nonetheless, early diagnosis and symptomatic therapy can profoundly influence …

Predictors of survival in progressive supranuclear palsy and multiple system atrophy: a systematic review and meta-analysis

SA Glasmacher, PN Leigh, RA Saha - Journal of Neurology …, 2017 - jnnp.bmj.com
Objective To undertake a systematic review and meta-analysis of studies that investigated
prognostic factors and survival in patients with progressive supranuclear palsy (PSP) and …

[HTML][HTML] Symptoms and quality of life in late stage Parkinson syndromes: a longitudinal community study of predictive factors

IJ Higginson, W Gao, TZ Saleem, KR Chaudhuri… - PloS one, 2012 - journals.plos.org
Background Palliative care is increasingly offered earlier in the cancer trajectory but rarely in
Idiopathic Parkinson's Disease (IPD), Progressive Supranuclear Palsy (PSP) or Multiple …

Genetic and epigenetic studies of amyotrophic lateral sclerosis

A Al-Chalabi, S Kwak, M Mehler… - … Lateral Sclerosis and …, 2013 - Taylor & Francis
The identification of genetic and epigenetic factors that are associated with an increased risk
of developing amyotrophic lateral sclerosis (ALS), or that modify the age of onset or rate of …

Accepting or declining non-invasive ventilation or gastrostomy in amyotrophic lateral sclerosis: patients' perspectives

LP Greenaway, NH Martin, V Lawrence, A Janssen… - Journal of …, 2015 - Springer
The objective was to identify factors associated with decisions made by patients with
amyotrophic lateral sclerosis (ALS) to accept or decline non-invasive ventilation (NIV) and/or …

[HTML][HTML] Mitochondrial abnormalities and low grade inflammation are present in the skeletal muscle of a minority of patients with amyotrophic lateral sclerosis; an …

S Al-Sarraj, A King, M Cleveland, PF Pradat… - Acta neuropathologica …, 2014 - Springer
Background Amyotrophic lateral sclerosis (ALS) is a primary progressive neurodegenerative
disease characterised by neuronal loss of lower motor neurons (in the spinal cord and …

The multidisciplinary care clinic: the principles and an international perspective

H Mitsumoto, GD Borasio, AL Genge… - NEUROLOGICAL …, 2006 - api.taylorfrancis.com
The Multidisciplinary Care Clinic: The Principles and an International Perspective Page 1 27
The Multidisciplinary Care Clinic: The Principles and an International Perspective Hiroshi …

Can NODDI provide a better characterisation of microstructural changes in ALS than DTI?

M Gabel, R Broad, DC Alexander, H Zhang, NG Dowell… - archive.ismrm.org
NODDI is a multi-compartment model of diffusion MRI that overcomes some of the limitations
of DTI. Our aim was to assess whether voxelwise analysis of NODDI parameters could …

CORRELATION ANALYSIS OF NEURITE ORIENTATION DISPERSION & DENSITY IMAGING IN MND

R Broad, M Gabel, N Dowell, G Zhang, D Alexander… - 2016 - jnnp.bmj.com
Background Neurite Orientation Dispersion and Density Imaging (NODDI) is an established
technique for estimating complexity of neuronal architecture. We used NODDI to …

[CITATION][C] Good practice in the management of amyotrophic lateral sclerosis: clinical guidelines. An evidence-based review with good practice points. EALSC …

PM Andersen, GD Borasio, R Dengler, O Hardiman… - dx. doi. org/10.1080 …