Progress in the pathogenesis of amyotrophic lateral sclerosis (Q34566352)

3 August 2017

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title

Progress in the pathogenesis of amyotrophic lateral sclerosis (English)

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amyotrophic lateral sclerosis

3 August 2017

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author name string

Shaw CE

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1

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3 August 2017

al-Chalabi A

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2

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3 August 2017

Leigh N

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3

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3 August 2017

1 January 2001

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Current Neurology and Neuroscience Reports

3 August 2017

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3 August 2017

1

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3 August 2017

1

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3 August 2017

69-76

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https://scigraph.springernature.com/pub.10.1007/s11910-001-0078-7

3 August 2017

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cites work

Spinobulbar muscular atrophy can mimic ALS: the importance of genetic testing in male patients with atypical ALS.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11910-001-0078-7

Familial amyotrophic lateral sclerosis. Molecular pathology of a patient with a SOD1 mutation.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11910-001-0078-7

Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.

21 January 2018

1 reference

12 December 2020

Autosomal dominant juvenile amyotrophic lateral sclerosis.

1 reference

12 December 2020

Induction of nitric oxide-dependent apoptosis in motor neurons by zinc-deficient superoxide dismutase

1 reference

12 December 2020

Selective loss of glial glutamate transporter GLT-1 in amyotrophic lateral sclerosis

1 reference

12 December 2020

Physical trauma and family history of neurodegenerative diseases in amyotrophic lateral sclerosis: a population-based case-control study

1 reference

12 December 2020

Absence of neurofilaments reduces the selective vulnerability of motor neurons and slows disease caused by a familial amyotrophic lateral sclerosis-linked superoxide dismutase 1 mutant

1 reference

12 December 2020

Remarkable increase in cerebrospinal fluid 3-nitrotyrosine in patients with sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

Possible relation of atypical parkinsonism in the French West Indies with consumption of tropical plants: a case-control study. Caribbean Parkinsonism Study Group

1 reference

12 December 2020

Amyotrophic lateral sclerosis: current issues in classification, pathogenesis and molecular pathology.

1 reference

12 December 2020

Superoxide dismutase and familial amyotrophic lateral sclerosis: new insights into mechanisms and treatments

1 reference

12 December 2020

Detection of reverse transcriptase activity in the serum of patients with motor neurone disease

1 reference

12 December 2020

Increased 3-nitrotyrosine and oxidative damage in mice with a human copper/zinc superoxide dismutase mutation.

1 reference

12 December 2020

Potential role of LIF as a modifier gene in the pathogenesis of amyotrophic lateral sclerosis

1 reference

12 December 2020

Oxidative damage to protein in sporadic motor neuron disease spinal cord

1 reference

12 December 2020

Longitudinal analysis of amyotrophic lateral sclerosis mortality in Norway, 1966-1989: evidence for a susceptible subpopulation

1 reference

12 December 2020

Decreased zinc affinity of amyotrophic lateral sclerosis-associated superoxide dismutase mutants leads to enhanced catalysis of tyrosine nitration by peroxynitrite

1 reference

12 December 2020

LIF (AM424), a promising growth factor for the treatment of ALS

1 reference

12 December 2020

Protective effect of neurofilament heavy gene overexpression in motor neuron disease induced by mutant superoxide dismutase

1 reference

12 December 2020

Mutations in all five exons ofSOD-1 may cause ALS

1 reference

12 December 2020

Neurofilament metabolism in sporadic amyotrophic lateral sclerosis.

1 reference

12 December 2020

Survival effect of ciliary neurotrophic factor (CNTF) on chick embryonic motoneurons in culture: comparison with other neurotrophic factors and cytokines.

1 reference

12 December 2020

A mutant neurofilament subunit causes massive, selective motor neuron death: implications for the pathogenesis of human motor neuron disease

1 reference

12 December 2020

Alternative splicing of the glutamate transporter EAAT2 (GLT-1).

1 reference

12 December 2020

Molecular genetic analysis of the APEX nuclease gene in amyotrophic lateral sclerosis

1 reference

12 December 2020

El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases a

1 reference

12 December 2020

ALS, SOD and peroxynitrite

1 reference

12 December 2020

Ciliary neurotrophic factor prevents degeneration of motor neurons in mouse mutant progressive motor neuronopathy

1 reference

12 December 2020

Variation in the biochemical/biophysical properties of mutant superoxide dismutase 1 enzymes and the rate of disease progression in familial amyotrophic lateral sclerosis kindreds.

1 reference

12 December 2020

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1 reference

12 December 2020

Mitochondrial enzyme activity in amyotrophic lateral sclerosis: implications for the role of mitochondria in neuronal cell death

1 reference

12 December 2020

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

1 reference

12 December 2020

Reduction of GluR2 RNA editing, a molecular change that increases calcium influx through AMPA receptors, selective in the spinal ventral gray of patients with amyotrophic lateral sclerosis

1 reference

12 December 2020

The expression of the glial glutamate transporter protein EAAT2 in motor neuron disease: an immunohistochemical study.

1 reference

12 December 2020

A receptor for advanced glycosylation endproducts (AGEs) is colocalized with neurofilament-bound AGEs and SOD1 in motoneurons of ALS: immunohistochemical study

1 reference

12 December 2020

Protein oxidative damage in a transgenic mouse model of familial amyotrophic lateral sclerosis

1 reference

12 December 2020

Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis

1 reference

12 December 2020

Development of central nervous system pathology in a murine transgenic model of human amyotrophic lateral sclerosis

1 reference

12 December 2020

Decreased glutamate transport by the brain and spinal cord in amyotrophic lateral sclerosis

1 reference

12 December 2020

Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALS.

1 reference

12 December 2020

Epilepsy and exacerbation of brain injury in mice lacking the glutamate transporter GLT-1

1 reference

12 December 2020

Advanced glycation endproducts in neurofilament conglomeration of motoneurons in familial and sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

Use of human intravenous immunoglobulin in lower motor neuron syndromes

1 reference

12 December 2020

Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis

1 reference

12 December 2020

Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis

1 reference

12 December 2020

Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis

1 reference

12 December 2020

Neurofilament subunit NF-H modulates axonal diameter by selectively slowing neurofilament transport

1 reference

12 December 2020

Glutamate slows axonal transport of neurofilaments in transfected neurons

1 reference

12 December 2020

Abnormal excitatory amino acid metabolism in amyotrophic lateral sclerosis

1 reference

12 December 2020

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

1 reference

12 December 2020

Detection and cellular localization of enterovirus RNA sequences in spinal cord of patients with ALS

1 reference

12 December 2020

Aggregation of mutant Cu/Zn superoxide dismutase proteins in a culture model of ALS

1 reference

12 December 2020

Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis

1 reference

12 December 2020

Increased 3-nitrotyrosine in both sporadic and familial amyotrophic lateral sclerosis

1 reference

12 December 2020

Late onset of motor neurons in mice overexpressing wild-type peripherin

1 reference

12 December 2020

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

1 reference

12 December 2020

Novel insertion in the KSP region of the neurofilament heavy gene in amyotrophic lateral sclerosis (ALS)

1 reference

12 December 2020

The RNA of the glutamate transporter EAAT2 is variably spliced in amyotrophic lateral sclerosis and normal individuals

1 reference

12 December 2020

Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.

1 reference

12 December 2020

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

1 reference

12 December 2020

Identification of alternative splicing forms of GLT-1 mRNA in the spinal cord of amyotrophic lateral sclerosis patients.

1 reference

12 December 2020

Coadministration of interleukin-6 (IL-6) and soluble IL-6 receptor delays progression of wobbler mouse motor neuron disease.

1 reference

12 December 2020

Mitochondria in sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

Population-based case-control study of amyotrophic lateral sclerosis in western Washington State. I. Cigarette smoking and alcohol consumption

1 reference

12 December 2020

Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients

1 reference

12 December 2020

Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

10.1007/S11910-001-0078-7

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3 August 2017

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