Neubauer B - Search Results

1

Clinical and genetic spectrum of SCN2A-associated episodic ataxia.

Schwarz N, Bast T, Gaily E, Golla G, Gorman KM, Griffiths LR, Hahn A, Hukin J, King M, Korff C, Miranda MJ, Møller RS, Neubauer B, Smith RA, Smol T, Striano P, Stroud B, Vaccarezza M, Kluger G, Lerche H, Fazeli W. Schwarz N, et al. Among authors: neubauer b. Eur J Paediatr Neurol. 2019 May;23(3):438-447. doi: 10.1016/j.ejpn.2019.03.001. Epub 2019 Mar 7. Eur J Paediatr Neurol. 2019. PMID: 30928199

2

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

3

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.

4

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

5

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.

6

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.

7

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.

8

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

9

[Autism and metabolic disorders-a rational approach].

Hahn A, Neubauer BA. Hahn A, et al. Z Kinder Jugendpsychiatr Psychother. 2005 Oct;33(4):259-71. doi: 10.1024/1422-4917.33.4.259. Z Kinder Jugendpsychiatr Psychother. 2005. PMID: 16294704 Review. German.

10

A new type of leukoencephalopathy with metaphyseal chondrodysplasia maps to Xq25-q27.

Neubauer BA, Stefanova I, Hübner CA, Neumaier-Probst E, Bohl J, Oppermann HC, Stö H, Hahn A, Stephani U, Kohlschütter A, Gal A. Neubauer BA, et al. Neurology. 2006 Aug 22;67(4):587-91. doi: 10.1212/01.wnl.0000230133.11951.75. Neurology. 2006. PMID: 16924009

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