Wilhelmina G. Leen
Nijmegen, GE, Netherlands
Last Updated: 09/26/2026
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Found 14 publications
Eye movement disorders in inborn errors of metabolism: A quantitative analysis of 37 patients.
Journal: Journal of inherited metabolic disease
Published: February 03, 2022
Head circumference in glucose transporter 1 deficiency syndrome: Normal for individuals, abnormal as a group.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: December 23, 2021
Upstream SLC2A1 translation initiation causes GLUT1 deficiency syndrome.
Journal: European journal of human genetics : EJHG
Published: October 02, 2016
Hourly analysis of cerebrospinal fluid glucose shows large diurnal fluctuations.
Journal: Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism
Published: December 09, 2015
Lactate and its many faces.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: February 17, 2015
A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood.
Journal: Cephalalgia : an international journal of headache
Published: May 15, 2014
Child neurology: differential diagnosis of a low CSF glucose in children and young adults.
Journal: Neurology
Published: December 11, 2013
GLUT1 deficiency syndrome into adulthood: a follow-up study.
Journal: Journal of neurology
Published: October 30, 2013
Cerebrospinal fluid analysis in the workup of GLUT1 deficiency syndrome: a systematic review.
Journal: JAMA neurology
Published: September 04, 2013
Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: February 12, 2013
Last Updated: 09/26/2026