Hypoglycorrhachia: A simple clue, simply missed [4]

Annals of Neurology

Volumn 49, Issue 5, 2001, Pages 685-686

  Willemsen, Michèl A A P ^a   Verrips, Aad ^a   Verbeek, Marcel M ^a   Voit, Thomas ^b   Klepper, Jörg ^b  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITY OF DUISBURG ESSEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSE; GLUCOSE TRANSPORTER;

ADOLESCENT; BLOOD BRAIN BARRIER; CEREBROSPINAL FLUID; CEREBROSPINAL FLUID LEVEL; CHILD; HUMAN; INFANT; LETTER; MAJOR CLINICAL STUDY; PRIORITY JOURNAL;

EID: 0035022288     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.1044     Document Type: Letter

References (5)

1. De Vivo DC, Trifiletti RR, Jacobson RI, et al. Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay. N Engl J Med 1991;325:703-709.
2. Seidner G, Garcia-Alvarez M, Yeh J-I, et al. GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier. Nat Genet 1998;18:188-191.
3. Klepper J, Garcia-Alvarez M, O'Driscoll KR, et al. Erythrocyte 3-O-methyl-D-glucose uptake assay for diagnosis of glucose-transporter-protein syndrome. J Clin Lab Anal 1999;13:116-121.
4. De Vivo DC, Garcia-Alvarez M, Ronen GM, Trifiletti RR. Glucose transport protein deficiency: an emerging syndrome with therapeutic implications. Int Pediatr 1995;10:51-56.
5. De Vivo DC, Burke C, Trifiletti R, et al. Glucose transporter protein deficiency: an emerging syndrome with therapeutic implications. Ann Neurol 1994;36:491.