Muhle H - Search Results

1

The role of SLC2A1 in early onset and childhood absence epilepsies.

Muhle H, Helbig I, Frøslev TG, Suls A, von Spiczak S, Klitten LL, Dahl HA, Brusgaard K, Neubauer B, De Jonghe P, Tommerup N, Stephani U, Hjalgrim H, Møller RS. Muhle H, et al. Epilepsy Res. 2013 Jul;105(1-2):229-33. doi: 10.1016/j.eplepsyres.2012.11.004. Epub 2013 Jan 8. Epilepsy Res. 2013. PMID: 23306390

2

Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspects.

Santer R, Muhle H, Suormala T, Baumgartner ER, Duran M, Yang X, Aoki Y, Suzuki Y, Stephani U. Santer R, et al. Among authors: muhle h. Mol Genet Metab. 2003 Jul;79(3):160-6. doi: 10.1016/s1096-7192(03)00091-x. Mol Genet Metab. 2003. PMID: 12855220

3

Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy.

Tauer U, Lorenz S, Lenzen KP, Heils A, Muhle H, Gresch M, Neubauer BA, Waltz S, Rudolf G, Mattheisen M, Strauch K, Nürnberg P, Schmitz B, Stephani U, Sander T. Tauer U, et al. Among authors: muhle h. Ann Neurol. 2005 Jun;57(6):866-73. doi: 10.1002/ana.20500. Ann Neurol. 2005. PMID: 15929039

4

Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity.

Lorenz S, Heils A, Taylor KP, Gehrmann A, Muhle H, Gresch M, Becker T, Tauer U, Stephani U, Sander T. Lorenz S, et al. Among authors: muhle h. Neurosci Lett. 2006 Apr 24;397(3):234-9. doi: 10.1016/j.neulet.2005.12.030. Epub 2006 Jan 6. Neurosci Lett. 2006. PMID: 16406321

5

Nonparalytic poliomyelitis in Lyme borreliosis.

van Baalen A, Muhle H, Straube T, Jansen O, Stephani U. van Baalen A, et al. Among authors: muhle h. Arch Dis Child. 2006 Aug;91(8):660. doi: 10.1136/adc.2006.098392. Arch Dis Child. 2006. PMID: 16861483 Free PMC article. No abstract available.

6

Spreading photoparoxysmal EEG response is associated with an abnormal cortical excitability pattern.

Siniatchkin M, Groppa S, Jerosch B, Muhle H, Kurth C, Shepherd AJ, Siebner H, Stephani U. Siniatchkin M, et al. Among authors: muhle h. Brain. 2007 Jan;130(Pt 1):78-87. doi: 10.1093/brain/awl306. Epub 2006 Nov 21. Brain. 2007. PMID: 17121743

7

Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.

Hempelmann A, Cobilanschi J, Heils A, Muhle H, Stephani U, Weber Y, Lerche H, Sander T. Hempelmann A, et al. Among authors: muhle h. Epilepsy Res. 2007 Apr;74(1):28-32. doi: 10.1016/j.eplepsyres.2006.12.001. Epub 2007 Jan 9. Epilepsy Res. 2007. PMID: 17215107

8

Hemodynamic responses to interictal epileptiform discharges in children with symptomatic epilepsy.

Jacobs J, Kobayashi E, Boor R, Muhle H, Stephan W, Hawco C, Dubeau F, Jansen O, Stephani U, Gotman J, Siniatchkin M. Jacobs J, et al. Among authors: muhle h. Epilepsia. 2007 Nov;48(11):2068-78. doi: 10.1111/j.1528-1167.2007.01192.x. Epub 2007 Jul 21. Epilepsia. 2007. PMID: 17645544 Free article.

9

Changes in activity of striato-thalamo-cortical network precede generalized spike wave discharges.

Moeller F, Siebner HR, Wolff S, Muhle H, Boor R, Granert O, Jansen O, Stephani U, Siniatchkin M. Moeller F, et al. Among authors: muhle h. Neuroimage. 2008 Feb 15;39(4):1839-49. doi: 10.1016/j.neuroimage.2007.10.058. Epub 2007 Nov 17. Neuroimage. 2008. PMID: 18082429

10

Childhood-onset restless legs syndrome: clinical and genetic features of 22 families.

Muhle H, Neumann A, Lohmann-Hedrich K, Lohnau T, Lu Y, Winkler S, Waltz S, Fischenbeck A, Kramer PL, Klein C, Stephani U. Muhle H, et al. Mov Disord. 2008 Jun 15;23(8):1113-21; quiz 1203. doi: 10.1002/mds.22016. Mov Disord. 2008. PMID: 18381645

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