Biomarkers in amyotrophic lateral sclerosis

MR Turner, MC Kiernan, PN Leigh, K Talbot - The Lancet Neurology, 2009 - thelancet.com
Amyotrophic lateral sclerosis (ALS; motor neuron disease) is a relentlessly progressive
disorder. After half a century of trials, only one drug with modest disease-modifying potency …

The management of motor neurone disease

PN Leigh, S Abrahams, A Al-Chalabi… - Journal of Neurology …, 2003 - jnnp.bmj.com
The management of motor neurone disease (MND) has evolved rapidly over the last two
decades. Although still incurable, MND is not untreatable. From an attitude of nihilism …

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

…, O Hardiman, K Kollewe, PN Leigh… - 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 …

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

…, V Tripathi, S Al-Saraj, A Al-Chalabi, PN Leigh… - Science, 2009 - science.org
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that is familial in
10% of cases. We have identified a missense mutation in the gene encoding fused in …

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

…, F Baralle, J De Belleroche, JD Mitchell, PN Leigh… - Science, 2008 - science.org
Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disorder characterized
pathologically by ubiquitinated TAR DNA binding protein (TDP-43) inclusions. The function …

Dose-ranging study of riluzole in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis/Riluzole Study Group II.

L Lacomblez, G Bensimon, PN Leigh… - Lancet (London …, 1996 - europepmc.org
Background Amyotrophic lateral sclerosis (ALS) is a progressive disease with no effective
treatment. In an initial study, riluzole decreased mortality and slowed muscle-strength …

Fronto-striatal cognitive deficits at different stages of Parkinson's disease

AM Owen, M James, PN Leigh, BA Summers… - Brain, 1992 - academic.oup.com
Groups of patients with idiopathic Parkinson's disease, either medicated or unmedicated,
were compared with matched groups of normal controls on a computerized battery …

Evidence of widespread cerebral microglial activation in amyotrophic lateral sclerosis: an [11C](R)-PK11195 positron emission tomography study

…, CCJ Miller, CE Shaw, DJ Brooks, PN Leigh… - Neurobiology of …, 2004 - Elsevier
Microglial activation is implicated in the pathogenesis of ALS and can be detected in animal
models of the disease that demonstrate increased survival when treated with anti …

Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis

…, C Shoesmith, J Rosenfeld, PN Leigh… - Amyotrophic Lateral …, 2009 - Taylor & Francis
Amyotrophic lateral sclerosis (ALS) is increasingly recognized to be a multisystem disorder
which includes both clinical and neuropathological features of a frontotemporal lobar …

Verbal fluency and executive dysfunction in amyotrophic lateral sclerosis (ALS)

S Abrahams, PN Leigh, A Harvey, GN Vythelingum… - Neuropsychologia, 2000 - Elsevier
Neuropsychological investigations of amyotrophic lateral sclerosis (ALS) patients have
revealed variable results on specific tests, despite a similar overall cognitive profile of …