Ringelstein EB - Search Results

1

Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14.

Kuhlenbäumer G, Lüdemann P, Schirmacher A, De Vriendt E, Hünermund G, Young P, Hund-Georgiadis M, Schuierer G, Möller H, Ringelstein EB, Van Broeckhoven C, Timmerman V, Stögbauer F. Kuhlenbäumer G, et al. Among authors: ringelstein eb. Neurology. 2004 Jun 22;62(12):2203-8. doi: 10.1212/01.wnl.0000130485.89814.10. Neurology. 2004. PMID: 15210883

2

Autosomal dominant burning feet syndrome.

Stögbauer F, Young P, Kuhlenbäumer G, Kiefer R, Timmerman V, Ringelstein EB, Wang JF, Schröder JM, Van Broeckhoven C, Weis J. Stögbauer F, et al. Among authors: ringelstein eb. J Neurol Neurosurg Psychiatry. 1999 Jul;67(1):78-81. doi: 10.1136/jnnp.67.1.78. J Neurol Neurosurg Psychiatry. 1999. PMID: 10369826 Free PMC article.

3

Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals.

Kuhlenbäumer G, Kress W, Ringelstein EB, Stögbauer F. Kuhlenbäumer G, et al. Among authors: ringelstein eb. J Neurol. 2001 Jan;248(1):23-6. doi: 10.1007/s004150170265. J Neurol. 2001. PMID: 11266016

4

Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25.

Stögbauer F, Young P, Timmerman V, Spoelders P, Ringelstein EB, Van Broeckhoven C, Kurlemann G. Stögbauer F, et al. Among authors: ringelstein eb. Hum Genet. 1997 May;99(5):685-7. doi: 10.1007/s004390050430. Hum Genet. 1997. PMID: 9150742

5

Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome.

Stögbauer F, Young P, Wiebusch H, Timmerman V, Kuhlenbäumer G, Nelis E, Ringelstein EB, Kurlemann G, Assmann G, Van Broeckhoven C, Funke H. Stögbauer F, et al. Among authors: ringelstein eb. Neurosci Lett. 1998 Jan 2;240(1):1-4. doi: 10.1016/s0304-3940(97)00887-2. Neurosci Lett. 1998. PMID: 9488160

6

PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1A.

Young P, Stögbauer F, Wiebusch H, Löfgren A, Timmerman V, Van Broeckhoven C, Ringelstein EB, Assmann G, Funke H. Young P, et al. Among authors: ringelstein eb. Neurology. 1998 Mar;50(3):760-3. doi: 10.1212/wnl.50.3.760. Neurology. 1998. PMID: 9521270

7

A second family with autosomal dominant burning feet syndrome.

Kuhlenbäumer G, Young P, Kiefer R, Timmerman V, Wang JF, Schroeder JM, Weis J, Ringelstein EB, Van Broeckhoven C, Stoegbauer F. Kuhlenbäumer G, et al. Among authors: ringelstein eb. Ann N Y Acad Sci. 1999 Sep 14;883:445-8. Ann N Y Acad Sci. 1999. PMID: 10586269 No abstract available.

8

Disturbed benzodiazepine receptor function at the onset of temporal lobe epilepsy--lomanzenil-binding in de-novo TLE.

Matheja P, Lüdemann P, Kuwert T, Weckesser M, Kellinghaus C, Weitemeyer L, Diehl B, Schuierer G, Ringelstein EB, Schober O. Matheja P, et al. Among authors: ringelstein eb. J Neurol. 2001 Jul;248(7):585-91. doi: 10.1007/s004150170136. J Neurol. 2001. PMID: 11518000

9

Pneumonia in acute stroke patients fed by nasogastric tube.

Dziewas R, Ritter M, Schilling M, Konrad C, Oelenberg S, Nabavi DG, Stögbauer F, Ringelstein EB, Lüdemann P. Dziewas R, et al. Among authors: ringelstein eb. J Neurol Neurosurg Psychiatry. 2004 Jun;75(6):852-6. doi: 10.1136/jnnp.2003.019075. J Neurol Neurosurg Psychiatry. 2004. PMID: 15145999 Free PMC article.

10

Generalized arteriopathy in patients with cervical artery dissection.

Völker W, Besselmann M, Dittrich R, Nabavi D, Konrad C, Dziewas R, Evers S, Grewe S, Krämer SC, Bachmann R, Stögbauer F, Ringelstein EB, Kuhlenbäumer G. Völker W, et al. Among authors: ringelstein eb. Neurology. 2005 May 10;64(9):1508-13. doi: 10.1212/01.WNL.0000159739.24607.98. Neurology. 2005. PMID: 15883309

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