Stephani U - Search Results

1

KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.

Neubauer BA, Waldegger S, Heinzinger J, Hahn A, Kurlemann G, Fiedler B, Eberhard F, Muhle H, Stephani U, Garkisch S, Eeg-Olofsson O, Müller U, Sander T. Neubauer BA, et al. Among authors: stephani u. Neurology. 2008 Jul 15;71(3):177-83. doi: 10.1212/01.wnl.0000317090.92185.ec. Neurology. 2008. PMID: 18625963

2

Benign childhood epilepsy with centrotemporal spikes and electroencephalography trait are not linked to EBN1 and EBN2 of benign neonatal familial convulsions.

Neubauer BA, Moises HW, Lässker U, Waltz S, Diebold U, Stephani U. Neubauer BA, et al. Among authors: stephani u. Epilepsia. 1997 Jul;38(7):782-7. doi: 10.1111/j.1528-1157.1997.tb01465.x. Epilepsia. 1997. PMID: 9579905 Free article.

3

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

Neubauer BA, Fiedler B, Himmelein B, Kämpfer F, Lässker U, Schwabe G, Spanier I, Tams D, Bretscher C, Moldenhauer K, Kurlemann G, Weise S, Tedroff K, Eeg-Olofsson O, Wadelius C, Stephani U. Neubauer BA, et al. Among authors: stephani u. Neurology. 1998 Dec;51(6):1608-12. doi: 10.1212/wnl.51.6.1608. Neurology. 1998. PMID: 9855510

4

Neuroborreliosis and isolated trochlear palsy.

Müller D, Neubauer BA, Waltz S, Stephani U. Müller D, et al. Among authors: stephani u. Eur J Paediatr Neurol. 1998;2(5):275-6. doi: 10.1016/s1090-3798(98)80042-1. Eur J Paediatr Neurol. 1998. PMID: 10726831

5

Neuropsychological long-term outcome of rolandic EEG traits.

Carlsson G, Igelbrink-Schulze N, Neubauer BA, Stephani U. Carlsson G, et al. Among authors: stephani u. Epileptic Disord. 2000;2 Suppl 1:S63-6. Epileptic Disord. 2000. PMID: 11231228 Free article.

6

Atypical "benign" partial epilepsy or pseudo-Lennox syndrome. Part I: symptomatology and long-term prognosis.

Hahn A, Pistohl J, Neubauer BA, Stephani U. Hahn A, et al. Among authors: stephani u. Neuropediatrics. 2001 Feb;32(1):1-8. doi: 10.1055/s-2001-12216. Neuropediatrics. 2001. PMID: 11315196

7

Atypical "benign" partial epilepsy of childhood or pseudo-lennox syndrome. Part II: family study.

Doose H, Hahn A, Neubauer BA, Pistohl J, Stephani U. Doose H, et al. Among authors: stephani u. Neuropediatrics. 2001 Feb;32(1):9-13. doi: 10.1055/s-2001-12215. Neuropediatrics. 2001. PMID: 11315204

8

Clinical spectrum and genetics of Rolandic epilepsy.

Neubauer BA, Hahn A, Stephani U, Doose H. Neubauer BA, et al. Among authors: stephani u. Adv Neurol. 2002;89:475-9. Adv Neurol. 2002. PMID: 11968472 Review. No abstract available.

9

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: stephani u. Mol Genet Metab. 2003 Jul;79(3):160-6. doi: 10.1016/s1096-7192(03)00091-x. Mol Genet Metab. 2003. PMID: 12855220

10

Genetics of photosensitivity (photoparoxysmal response): a review.

Stephani U, Tauer U, Koeleman B, Pinto D, Neubauer BA, Lindhout D. Stephani U, et al. Epilepsia. 2004;45 Suppl 1:19-23. doi: 10.1111/j.0013-9580.2004.451008.x. Epilepsia. 2004. PMID: 14706040 Free article. Review.

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