Related references
Note: Only part of the references are listed.Advanced statistical methods to study the effects of gastric tube and non-invasive ventilation on functional decline and survival in amyotrophic lateral sclerosis
Nazem Atassi et al.
AMYOTROPHIC LATERAL SCLEROSIS (2011)
Respiratory onset in an ALS family with L144F SOD1 mutation
P. Corcia et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)
Large-scale SOD1 mutation screening provides evidence for genetic heterogeneity in amyotrophic lateral sclerosis
Michael A. van Es et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2010)
A population-based study of genotypic and phenotypic variability in children with spinal muscular atrophy
Eva Arkblad et al.
ACTA PAEDIATRICA (2009)
Recent advances in the genetics of amyotrophic lateral sclerosis
Paul N. Valdmanis et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2009)
Association of APOE with age at onset of sporadic amyotrophic lateral sclerosis
Henrik Zetterberg et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2008)
APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy
Kristel Sleegers et al.
BRAIN (2006)
The epidemiology of ALS and the role of population-based registries
Ettore Beghi et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2006)
SMN1 gene, but not SMN2, is a risk factor for sporadic ALS
P. Corcia et al.
NEUROLOGY (2006)
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis
MJ Greenway et al.
NATURE GENETICS (2006)
Spinal muscular atrophy: the RNP connection
C Eggert et al.
TRENDS IN MOLECULAR MEDICINE (2006)
Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene
Peter M. Andersen
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2006)
SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS
JH Veldink et al.
NEUROLOGY (2005)
Causal relation between α-synuclein gene duplication and familial Parkinson's disease
P Ibáñez et al.
LANCET (2004)
Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis
P Corcia et al.
ANNALS OF NEUROLOGY (2002)
Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): A potential susceptibility factor for adult-onset lower motor neuron disease
A Echaniz-Laguna et al.
JOURNAL OF NEUROLOGY (2002)
Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS
JH Veldink et al.
NEUROLOGY (2001)
El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis
BR Brooks et al.
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS (2000)