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Jörg Klepper

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Chemicals & Drugs

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All Publications

2013: Jörg Klepper
Glucide metabolism disorders (excluding glycogen myopathies).
Handbook of clinical neurology 2013;113():1689-94.
2008: Jörg Klepper
Glucose transporter deficiency syndrome (GLUT1DS) and the ketogenic diet.
Epilepsia 2008;49 Suppl 8():46-9.
2007: Jörg Klepper; Bärbel Leiendecker
GLUT1 deficiency syndrome--2007 update.
Developmental medicine and child neurology 2007;49(9):707-16.
2007: Jörg Klepper; Volkher Engelbrecht; Hans Scheffer; Marjo S van der Knaap; Andreas Fiedler
GLUT1 deficiency with delayed myelination responding to ketogenic diet.
Pediatric neurology 2007;37(2):130-3.
2006: Bärbel Leiendecker; Jörg Klepper
[The ketogenic diet -- role of the pediatric nurse].
Kinderkrankenschwester : Organ der Sektion Kinderkrankenpflege / Deutsche Gesellschaft für Sozialpädiatrie und Deutsche Gesellschaft für Kinderheilkunde 2006;25(12):514-7.
2005: Jörg Klepper; Hans Scheffer; Bärbel Leiendecker; Elena Gertsen; S Binder; M Leferink; Christoph Hertzberg; A Näke; Thomas Voit; Michèl A A P Willemsen
Seizure control and acceptance of the ketogenic diet in GLUT1 deficiency syndrome: a 2- to 5-year follow-up of 15 children enrolled prospectively.
Neuropediatrics 2005;36(5):302-8.
2005: Jörg Klepper; Alexis Salas-Burgos; Elena Gertsen; Jorge Fischbarg
Bench meets bedside: a 10-year-old girl and amino acid residue glycine 75 of the facilitative glucose transporter GLUT1.
Biochemistry 2005;44(38):12621-6.
2005: Yasushi Ito; Elena Gertsen; Hirokazu Oguni; Tomohiro Nakayama; Mari Matsuo; Makoto Funatsuka; Thomas Voit; Jörg Klepper; Makiko Osawa
Clinical presentation, EEG studies, and novel mutations in two cases of GLUT1 deficiency syndrome in Japan.
Brain & development 2005;27(4):311-7.
2004: Jörg Klepper; Bärbel Leiendecker; E Riemann; F A M Baumeister
[The ketogenic diet in German-speaking countries: update 2003].
Klinische Pädiatrie 2004;216(5):277-85.
2004: Jörg Klepper
Impaired glucose transport into the brain: the expanding spectrum of glucose transporter type 1 deficiency syndrome.
Current opinion in neurology 2004;17(2):193-6.
2004: Jörg Klepper; Sonja Diefenbach; Alfried Kohlschuetter; Thomas Voit
Effects of the ketogenic diet in the glucose transporter 1 deficiency syndrome.
Prostaglandins, leukotrienes, and essential fatty acids 2004;70(3):321-7.
2003: Peter Lange; Elena Gertsen; Ingrid Monden; Jörg Klepper; Konrad Keller
Functional consequences of an in vivo mutation in exon 10 of the human GLUT1 gene.
FEBS letters 2003;555(2):274-8.
2003: Jörg Klepper; Darryl C De Vivo; David W Webb; Lars Klinge; Thomas Voit
Reversible infantile hypoglycorrhachia: possible transient disturbance in glucose transport?
Pediatric neurology 2003;29(4):321-5.
2003: Michèl A A P Willemsen; R J Soorani-Lunsing; E Pouwels; Jörg Klepper
Neuroglycopenia in normoglycaemic patients, and the potential benefit of ketosis.
Diabetic medicine : a journal of the British Diabetic Association 2003;20(6):481-2.
2003: Jörg Klepper; Anne Flörcken; Jorge Fischbarg; Thomas Voit
Effects of anticonvulsants on GLUT1-mediated glucose transport in GLUT1 deficiency syndrome in vitro.
European journal of pediatrics 2003;162(2):84-9.
2002: Jörg Klepper; Bärbel Leiendecker; R Bredahl; S Athanassopoulos; Florian Heinen; Elena Gertsen; Anne Flörcken; A Metz; Thomas Voit
Introduction of a ketogenic diet in young infants.
Journal of inherited metabolic disease 2002;25(6):449-60.
2001: Y Ho; Hong Yang; Jörg Klepper; Jorge Fischbarg; Dong Wang; Darryl C De Vivo
Glucose transporter type 1 deficiency syndrome (Glut1DS): methylxanthines potentiate GLUT1 haploinsufficiency in vitro.
Pediatric research 2001;50(2):254-60.
2001: Jörg Klepper; Ingrid Monden; E Guertsen; Thomas Voit; Michèl A A P Willemsen; Konrad Keller
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
FEBS letters 2001;498(1):104-9.
2001: Michèl A A P Willemsen; Aad Verrips; M M Verbeek; Thomas Voit; Jörg Klepper
Hypoglycorrhachia: a simple clue, simply missed.
Annals of neurology 2001;49(5):685-6.
2001: Jörg Klepper; Michèl A A P Willemsen; Aad Verrips; E Guertsen; R Herrmann; C Kutzick; Anne Flörcken; Thomas Voit
Autosomal dominant transmission of GLUT1 deficiency.
Human molecular genetics 2001;10(1):63-8.
1999: Jörg Klepper; Jorge Fischbarg; Juan Carlos C Vera; Dong Wang; Darryl C De Vivo
GLUT1-deficiency: barbiturates potentiate haploinsufficiency in vitro.
Pediatric research 1999;46(6):677-83.
1999: Jörg Klepper; Dong Wang; Jorge Fischbarg; Juan Carlos C Vera; I T Jarjour; Kevin O'Driscoll; Darryl C De Vivo
Defective glucose transport across brain tissue barriers: a newly recognized neurological syndrome.
Neurochemical research 1999;24(4):587-94.
1999: Jörg Klepper; M Garcia-Alvarez; Kevin O'Driscoll; Michael K Parides; Dong Wang; Y Ho; Darryl C De Vivo
Erythrocyte 3-O-methyl-D-glucose uptake assay for diagnosis of glucose-transporter-protein syndrome.
Journal of clinical laboratory analysis 1999;13(3):116-21.
1998: Jörg Klepper; Juan Carlos C Vera; Darryl C De Vivo
Deficient transport of dehydroascorbic acid in the glucose transporter protein syndrome.
Annals of neurology 1998;44(2):286-7.
1998: G Seidner; M G Alvarez; J I Yeh; Kevin O'Driscoll; Jörg Klepper; T S Stump; Dong Wang; N B Spinner; M J Birnbaum; Darryl C De Vivo
GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier.
Nature genetics 1998;18(2):188-91.