Stephani U - Search Results

1

Beneficial prenatal levodopa therapy in autosomal recessive guanosine triphosphate cyclohydrolase 1 deficiency.

Brüggemann N, Spiegler J, Hellenbroich Y, Opladen T, Schneider SA, Stephani U, Boor R, Gillessen-Kaesbach G, Sperner J, Klein C. Brüggemann N, et al. Among authors: stephani u. Arch Neurol. 2012 Aug;69(8):1071-5. doi: 10.1001/archneurol.2012.104. Arch Neurol. 2012. PMID: 22473768

2

Cerebral proton magnetic resonance spectroscopy in infantile Alexander disease.

Brockmann K, Dechent P, Meins M, Haupt M, Sperner J, Stephani U, Frahm J, Hanefeld F. Brockmann K, et al. Among authors: stephani u. J Neurol. 2003 Mar;250(3):300-6. doi: 10.1007/s00415-003-0995-2. J Neurol. 2003. PMID: 12638020

3

Spatial filters and automated spike detection based on brain topographies improve sensitivity of EEG-fMRI studies in focal epilepsy.

Siniatchkin M, Moeller F, Jacobs J, Stephani U, Boor R, Wolff S, Jansen O, Siebner H, Scherg M. Siniatchkin M, et al. Among authors: stephani u. Neuroimage. 2007 Sep 1;37(3):834-43. doi: 10.1016/j.neuroimage.2007.05.049. Epub 2007 Jun 7. Neuroimage. 2007. PMID: 17627849

4

Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?

Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C. Lohmann-Hedrich K, et al. Among authors: stephani u. Neurology. 2008 Feb 26;70(9):686-94. doi: 10.1212/01.wnl.0000282760.07650.ba. Epub 2007 Nov 21. Neurology. 2008. PMID: 18032746

5

Myoclonus-dystonia: significance of large SGCE deletions.

Grünewald A, Djarmati A, Lohmann-Hedrich K, Farrell K, Zeller JA, Allert N, Papengut F, Petersen B, Fung V, Sue CM, O'Sullivan D, Mahant N, Kupsch A, Chuang RS, Wiegers K, Pawlack H, Hagenah J, Ozelius LJ, Stephani U, Schuit R, Lang AE, Volkmann J, Münchau A, Klein C. Grünewald A, et al. Among authors: stephani u. Hum Mutat. 2008 Feb;29(2):331-2. doi: 10.1002/humu.9521. Hum Mutat. 2008. PMID: 18205193

6

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. Among authors: stephani u. Mov Disord. 2008 Jun 15;23(8):1113-21; quiz 1203. doi: 10.1002/mds.22016. Mov Disord. 2008. PMID: 18381645

7

Non-REM sleep influences results of fMRI studies in epilepsy.

Moehring J, Moeller F, Jacobs J, Wolff S, Boor R, Jansen O, Stephani U, Siniatchkin M. Moehring J, et al. Among authors: stephani u. Neurosci Lett. 2008 Oct 3;443(2):61-6. doi: 10.1016/j.neulet.2008.07.044. Epub 2008 Jul 22. Neurosci Lett. 2008. PMID: 18657595

8

Hemodynamic changes preceding the interictal EEG spike in patients with focal epilepsy investigated using simultaneous EEG-fMRI.

Jacobs J, Levan P, Moeller F, Boor R, Stephani U, Gotman J, Siniatchkin M. Jacobs J, et al. Among authors: stephani u. Neuroimage. 2009 May 1;45(4):1220-31. doi: 10.1016/j.neuroimage.2009.01.014. Epub 2009 Jan 23. Neuroimage. 2009. PMID: 19349236

9

Febrile infection-related epilepsy syndrome (FIRES): a nonencephalitic encephalopathy in childhood.

van Baalen A, Häusler M, Boor R, Rohr A, Sperner J, Kurlemann G, Panzer A, Stephani U, Kluger G. van Baalen A, et al. Among authors: stephani u. Epilepsia. 2010 Jul;51(7):1323-8. doi: 10.1111/j.1528-1167.2010.02535.x. Epub 2010 Mar 18. Epilepsia. 2010. PMID: 20345937 Free article.

10

Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene.

Caliebe A, Kroes HY, van der Smagt JJ, Martin-Subero JI, Tönnies H, van 't Slot R, Nievelstein RA, Muhle H, Stephani U, Alfke K, Stefanova I, Hellenbroich Y, Gillessen-Kaesbach G, Hochstenbach R, Siebert R, Poot M. Caliebe A, et al. Among authors: stephani u. Eur J Med Genet. 2010 Jul-Aug;53(4):179-85. doi: 10.1016/j.ejmg.2010.04.001. Epub 2010 Apr 9. Eur J Med Genet. 2010. PMID: 20382278

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