Voit T - Search Results

1

Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease).

Oliveira JR, Spiteri E, Sobrido MJ, Hopfer S, Klepper J, Voit T, Gilbert J, Wszolek ZK, Calne DB, Stoessl AJ, Hutton M, Manyam BV, Boller F, Baquero M, Geschwind DH. Oliveira JR, et al. Among authors: voit t. Neurology. 2004 Dec 14;63(11):2165-7. doi: 10.1212/01.wnl.0000145601.88274.88. Neurology. 2004. PMID: 15596772 Free article.

2

Reversible infantile hypoglycorrhachia: possible transient disturbance in glucose transport?

Klepper J, De Vivo DC, Webb DW, Klinge L, Voit T. Klepper J, et al. Among authors: voit t. Pediatr Neurol. 2003 Oct;29(4):321-5. doi: 10.1016/s0887-8994(03)00268-6. Pediatr Neurol. 2003. PMID: 14643395

3

Hypoglycorrhachia: a simple clue, simply missed.

Willemsen MA, Verrips A, Verbeek MM, Voit T, Klepper J. Willemsen MA, et al. Among authors: voit t. Ann Neurol. 2001 May;49(5):685-6. Ann Neurol. 2001. PMID: 11357965 No abstract available.

4

Facilitated glucose transporter protein type 1 (GLUT1) deficiency syndrome: impaired glucose transport into brain-- a review.

Klepper J, Voit T. Klepper J, et al. Among authors: voit t. Eur J Pediatr. 2002 Jun;161(6):295-304. doi: 10.1007/s00431-002-0939-3. Epub 2002 Apr 16. Eur J Pediatr. 2002. PMID: 12029447 Review.

5

Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease.

Cormand B, Pihko H, Bayés M, Valanne L, Santavuori P, Talim B, Gershoni-Baruch R, Ahmad A, van Bokhoven H, Brunner HG, Voit T, Topaloglu H, Dobyns WB, Lehesjoki AE. Cormand B, et al. Among authors: voit t. Neurology. 2001 Apr 24;56(8):1059-69. doi: 10.1212/wnl.56.8.1059. Neurology. 2001. PMID: 11320179

6

Progressive dystonia in a 12-year-old boy.

Klepper J, Schaper J, Raca G, Coryell J, Das S, Hayflick SJ, Voit T. Klepper J, et al. Among authors: voit t. Eur J Paediatr Neurol. 2003;7(2):85-8. doi: 10.1016/s1090-3798(03)00019-9. Eur J Paediatr Neurol. 2003. PMID: 12697433

7

Effects of the ketogenic diet in the glucose transporter 1 deficiency syndrome.

Klepper J, Diefenbach S, Kohlschütter A, Voit T. Klepper J, et al. Among authors: voit t. Prostaglandins Leukot Essent Fatty Acids. 2004 Mar;70(3):321-7. doi: 10.1016/j.plefa.2003.07.004. Prostaglandins Leukot Essent Fatty Acids. 2004. PMID: 14769490

8

Effects of anticonvulsants on GLUT1-mediated glucose transport in GLUT1 deficiency syndrome in vitro.

Klepper J, Flörcken A, Fischbarg J, Voit T. Klepper J, et al. Among authors: voit t. Eur J Pediatr. 2003 Feb;162(2):84-9. doi: 10.1007/s00431-002-1112-8. Epub 2002 Dec 6. Eur J Pediatr. 2003. PMID: 12548383

9

Autosomal dominant transmission of GLUT1 deficiency.

Klepper J, Willemsen M, Verrips A, Guertsen E, Herrmann R, Kutzick C, Flörcken A, Voit T. Klepper J, et al. Among authors: voit t. Hum Mol Genet. 2001 Jan 1;10(1):63-8. doi: 10.1093/hmg/10.1.63. Hum Mol Genet. 2001. PMID: 11136715

10

Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.

Klepper J, Monden I, Guertsen E, Voit T, Willemsen M, Keller K. Klepper J, et al. Among authors: voit t. FEBS Lett. 2001 Jun 1;498(1):104-9. doi: 10.1016/s0014-5793(01)02463-2. FEBS Lett. 2001. PMID: 11389907 Free article.

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