Muhle H - Search Results

1

Hashimoto encephalopathy in a 15-year-old-girl: EEG findings and follow-up.

Muhle H, van Baalen A, Riepe FG, Rohr A, Stephani U. Muhle H, et al. Pediatr Neurol. 2009 Oct;41(4):301-4. doi: 10.1016/j.pediatrneurol.2009.04.023. Pediatr Neurol. 2009. PMID: 19748053

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

Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy.

Kearney JA, Wiste AK, Stephani U, Trudeau MM, Siegel A, RamachandranNair R, Elterman RD, Muhle H, Reinsdorf J, Shields WD, Meisler MH, Escayg A. Kearney JA, et al. Among authors: muhle h. Pediatr Neurol. 2006 Feb;34(2):116-20. doi: 10.1016/j.pediatrneurol.2005.07.009. Pediatr Neurol. 2006. PMID: 16458823

6

Association of BRD2 polymorphisms with photoparoxysmal response.

Lorenz S, Taylor KP, Gehrmann A, Becker T, Muhle H, Gresch M, Tauer U, Sander T, Stephani U. Lorenz S, et al. Among authors: muhle h. Neurosci Lett. 2006 May 29;400(1-2):135-9. doi: 10.1016/j.neulet.2006.02.026. Epub 2006 Mar 3. Neurosci Lett. 2006. PMID: 16516380

7

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.

8

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

9

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

10

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.

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