Work

The spectrum of movement disorders in Glut‐1 deficiency

Year: 2010

Type: article

Study design: Observational Study

Source: Movement Disorders

DOI: 10.1002/mds.22808

Authors: Roser Pons, Abbie Collins, Michael Rotstein, Kristin Engelstad, Darryl C De Vivo

Institutions: National and Kapodistrian University of Athens, Children's Hospital Agia Sophia, University of Colorado Denver, Columbia University

Language: English

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Spinal Muscular Atrophy Foundation, National Institutes of Health, U.S. Public Health Service, National Institute of Neurological Disorders and Stroke, National Center for Research Resources, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G2414565262, Clinical and Translational Science Award, G5636137340, G6358459586, NEUROGLYCOPENIA: GENOTYPE-PHENOTYPE CORRELATION

OpenAlex ID: W1909814622

FWCI: 7.861

Cites: 21

Cited by: 176

Related to: 10