Biomarkers in amyotrophic lateral sclerosis
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 …
disorder. After half a century of trials, only one drug with modest disease-modifying potency …
The management of motor neurone disease
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 …
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 …
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 …
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
Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disorder characterized
pathologically by ubiquitinated TAR DNA binding protein (TDP-43) inclusions. The function …
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 …
treatment. In an initial study, riluzole decreased mortality and slowed muscle-strength …
Fronto-striatal cognitive deficits at different stages of Parkinson's disease
Groups of patients with idiopathic Parkinson's disease, either medicated or unmedicated,
were compared with matched groups of normal controls on a computerized battery …
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
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 …
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 …
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 …
revealed variable results on specific tests, despite a similar overall cognitive profile of …