Neubauer BA - Search Results

1

Investigation of GRIN2A in common epilepsy phenotypes.

Lal D, Steinbrücker S, Schubert J, Sander T, Becker F, Weber Y, Lerche H, Thiele H, Krause R, Lehesjoki AE, Nürnberg P, Palotie A, Neubauer BA, Muhle H, Stephani U, Helbig I, Becker AJ, Schoch S, Hansen J, Dorn T, Hohl C, Lüscher N; Epicure consortium; EuroEPINOMICS-CoGIE consortium; von Spiczak S, Lemke JR. Lal D, et al. Among authors: neubauer ba. Epilepsy Res. 2015 Sep;115:95-9. doi: 10.1016/j.eplepsyres.2015.05.010. Epub 2015 Jun 2. Epilepsy Res. 2015. PMID: 26220384

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. 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. 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: neubauer ba. 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

Preponderance of female sex in the transmission of seizure liability in idiopathic generalized epilepsy.

Doose H, Neubauer BA. Doose H, et al. Among authors: neubauer ba. Epilepsy Res. 2001 Feb;43(2):103-14. doi: 10.1016/s0920-1211(00)00182-0. Epilepsy Res. 2001. PMID: 11164699

6

Neuropsychological long-term outcome of rolandic EEG traits.

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

7

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: neubauer ba. Neuropediatrics. 2001 Feb;32(1):1-8. doi: 10.1055/s-2001-12216. Neuropediatrics. 2001. PMID: 11315196

8

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: neubauer ba. Neuropediatrics. 2001 Feb;32(1):9-13. doi: 10.1055/s-2001-12215. Neuropediatrics. 2001. PMID: 11315204

9

Mutation analysis of the potassium chloride cotransporter KCC3 (SLC12A6) in rolandic and idiopathic generalized epilepsy.

Steinlein OK, Neubauer BA, Sander T, Song L, Stoodt J, Mount DB. Steinlein OK, et al. Among authors: neubauer ba. Epilepsy Res. 2001 May;44(2-3):191-5. doi: 10.1016/s0920-1211(01)00230-3. Epilepsy Res. 2001. PMID: 11325574

10

Occipital sharp waves in idiopathic partial epilepsies--clinical and genetic aspects.

Doose H, Petersen B, Neubauer BA. Doose H, et al. Among authors: neubauer ba. Epilepsy Res. 2002 Jan;48(1-2):121-30. doi: 10.1016/s0920-1211(01)00324-2. Epilepsy Res. 2002. PMID: 11823116

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