Neubauer BA - Search Results

1

Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia.

Schwarz N, Hahn A, Bast T, Müller S, Löffler H, Maljevic S, Gaily E, Prehl I, Biskup S, Joensuu T, Lehesjoki AE, Neubauer BA, Lerche H, Hedrich UBS. Schwarz N, et al. Among authors: neubauer ba. J Neurol. 2016 Feb;263(2):334-343. doi: 10.1007/s00415-015-7984-0. Epub 2015 Dec 8. J Neurol. 2016. PMID: 26645390

2

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

3

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

4

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

5

Clinical spectrum and genetics of Rolandic epilepsy.

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

6

X-linked lissencephaly with abnormal genitalia associated with renal phosphate wasting.

Hahn A, Gross C, Uyanik G, Hehr U, Hügens-Penzel M, Alzen G, Neubauer BA. Hahn A, et al. Among authors: neubauer ba. Neuropediatrics. 2004 Jun;35(3):202-5. doi: 10.1055/s-2004-817955. Neuropediatrics. 2004. PMID: 15248105

7

Myoclonic-astatic epilepsy of early childhood--definition, course, nosography, and genetics.

Neubauer BA, Hahn A, Doose H, Tuxhorn I. Neubauer BA, et al. Adv Neurol. 2005;95:147-55. Adv Neurol. 2005. PMID: 15508920 Review. No abstract available.

8

Photosensitivity: genetics and clinical significance.

Neubauer BA, Waltz S, Grothe M, Hahn A, Tuxhorn I, Sander T, Kurlemann G, Stephani U. Neubauer BA, et al. Adv Neurol. 2005;95:217-26. Adv Neurol. 2005. PMID: 15508925 No abstract available.

9

SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures.

Ebach K, Joos H, Doose H, Stephani U, Kurlemann G, Fiedler B, Hahn A, Hauser E, Hundt K, Holthausen H, Müller U, Neubauer BA. Ebach K, et al. Among authors: neubauer ba. Neuropediatrics. 2005 Jun;36(3):210-3. doi: 10.1055/s-2005-865607. Neuropediatrics. 2005. PMID: 15944908 Free article.

10

Late-onset nephrotic syndrome and severe cerebellar atrophy in Galloway-Mowat syndrome.

Steiss JO, Gross S, Neubauer BA, Hahn A. Steiss JO, et al. Among authors: neubauer ba. Neuropediatrics. 2005 Oct;36(5):332-5. doi: 10.1055/s-2005-872842. Neuropediatrics. 2005. PMID: 16217710

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