The EAAT2 (GLT-1) gene in motor neuron disease: absence of mutations in amyotrophic lateral sclerosis and a point mutation in patients with hereditary spastic paraplegia

El escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis

1994 • 2,090 citations

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

1995 • 1,430 citations

The release and uptake of excitatory amino acids

1990 • 1,090 citations

Functional comparisons of three glutamate transporter subtypes cloned from human motor cortex

1994 • 988 citations

Handbook of clinical neurology

1993 • 593 citations

Cloning and expression of a human neutral amino acid transporter with structural similarity to the glutamate transporter gene family

1993 • 387 citations

Hereditary Spastic Paraplegia

1996 • 195 citations

Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2

1996 • 82 citations

Genomic organization of the human excitatory amino acid transporter gene GLT-1

1997 • 36 citations

Familial Spastic Paraplegia

2011 • 36 citations

The glial glutamate transporter complementary DNA in patients with amyotrophic lateral sclerosis

1996 • 32 citations

Familial Spastic Paraplegia

2009 • 5 citations