Related references
Note: Only part of the references are listed.The glucose transporter type 1 (Glut1) syndromes
Henner Koch et al.
EPILEPSY & BEHAVIOR (2019)
Overall cognitive profiles in patients with GLUT1 Deficiency Syndrome
Valentina De Giorgis et al.
BRAIN AND BEHAVIOR (2019)
SLC2A1 mutations are a rare cause of pediatric-onset hereditary spastic paraplegia
Francesco Nicita et al.
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY (2019)
Stroke mimics add to the phenotypic spectrum of GLUT1 deficiency syndrome
Hilde M. H. Braakman et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2018)
Characteristic proton magnetic resonance spectroscopy in glucose transporter type 1 deficiency syndrome
Manami Akasaka et al.
PEDIATRICS INTERNATIONAL (2018)
GLUT1-deficiency syndrome: Report of a four-generation Norwegian family with a mild phenotype
Anette Ramm-Pettersen et al.
EPILEPSY & BEHAVIOR (2017)
Paroxysmal eye-head movements in Glut1 deficiency syndrome
Toni S. Pearson et al.
NEUROLOGY (2017)
Pathogenic mutations causing glucose transport defects in GLUT1 transporter: The role of intermolecular forces in protein structure-function
Mobeen Raja et al.
BIOPHYSICAL CHEMISTRY (2015)
From splitting GLUT1 deficiency syndromes to overlapping phenotypes
Marie Hully et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2015)
GLUT1 deficiency syndrome: An update
D. Gras et al.
REVUE NEUROLOGIQUE (2014)
Child Neurology: Differential diagnosis of a low CSF glucose in children and young adults
Wilhelmina G. Leen et al.
NEUROLOGY (2013)
Glut1 Deficiency: Inheritance Pattern Determined by Haploinsufficiency
Michael Rotstein et al.
ANNALS OF NEUROLOGY (2010)
The Spectrum of Movement Disorders in Glut-1 Deficiency
Roser Pons et al.
MOVEMENT DISORDERS (2010)
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak
Yvonne G. Weber et al.
JOURNAL OF CLINICAL INVESTIGATION (2008)
Familial paroxysmal exercise-induced dyskinesia and benign epilepsy: a clinical and neurophysiological study of an uncommon disorder
L Margari et al.
NEUROLOGICAL SCIENCES (2000)