A double-blind randomized clinical trial in amyotrophic lateral sclerosis using lamotrigine: effects on CSF glutamate, aspartate, branched-chain amino acid levels and clinical parameters (Q44478465)

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English	A double-blind randomized clinical trial in amyotrophic lateral sclerosis using lamotrigine: effects on CSF glutamate, aspartate, branched-chain amino acid levels and clinical parameters	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

A double-blind randomized clinical trial in amyotrophic lateral sclerosis using lamotrigine: effects on CSF glutamate, aspartate, branched-chain amino acid levels and clinical parameters (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

amyotrophic lateral sclerosis

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author name string

H Ryberg

1

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Europe PubMed Central

PubMed publication ID

3 December 2017

H Askmark

2

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3 December 2017

L I Persson

3

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3 December 2017

language of work or name

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publication date

1 July 2003

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Europe PubMed Central

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3 December 2017

Acta Neurologica Scandinavica

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3 December 2017

108

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Europe PubMed Central

PubMed publication ID

3 December 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

1-8

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

The role of excitotoxicity in neurodegenerative disease: implications for therapy

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Differential inhibition by riluzole, lamotrigine, and phenytoin of sodium and calcium currents in cortical neurons: implications for neuroprotective strategies

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Analysis of CSF amino acids in young patients with generalised refractory epilepsy during an add-on study with lamotrigine.

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A novel neuroprotective mechanism of riluzole: direct inhibition of protein kinase C.

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

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A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group

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

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Branched-chain amino acids and ALS

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Branched-chain amino acids and amyotrophic lateral sclerosis: a treatment failure? The Italian ALS Study Group

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Cortical excitability in amyotrophic lateral sclerosis: a clue to pathogenesis.

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Prevention by lamotrigine, MK-801 and N omega-nitro-L-arginine methyl ester of motoneuron cell death after neonatal axotomy

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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

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The administration of guanidine in amyotrophic lateral sclerosis

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A method of quantification for the evaluation of antiepileptic drug therapy

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Fasting plasma and CSF amino acid levels in amyotrophic lateral sclerosis: a subtype analysis.

1 reference

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Abnormal excitatory amino acid metabolism in amyotrophic lateral sclerosis

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7 January 2021

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

1 reference

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7 January 2021

based on heuristic

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

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7 January 2021

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Pilot trial of branched-chain aminoacids in amyotrophic lateral sclerosis

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Branched-chain amino acids in the treatment of amyotrophic lateral sclerosis.

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A pilot trial of dextromethorphan in amyotrophic lateral sclerosis

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Pharmacological studies on lamotrigine, a novel potential antiepileptic drug: II. Neurochemical studies on the mechanism of action

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Separation of amino acid enantiomers and chiral amines using precolumn derivatization with (+)-1-(9-fluorenyl)ethyl chloroformate and reversed-phase liquid chromatography

1 reference

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Changes in CSF amino acid concentrations during the evolution of amyotrophic lateral sclerosis

1 reference

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Brain metabolism of branched-chain amino acids

1 reference

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7 January 2021

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Identifiers

10.1034/J.1600-0404.2003.00111.X

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

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