Kuhlenbäumer G - Search Results

1

Characterizing mixed location hemorrhages/microbleeds with CSF markers.

Jensen-Kondering U, Margraf NG, Weiler C, Maetzler W, Dargvainiene J, Falk K, Philippen S, Bartsch T, Flüh C, Röcken C, Möller B, Royl G, Neumann A, Brüggemann N, Roeben B, Schulte C, Bender B, Berg D, Kuhlenbäumer G. Jensen-Kondering U, et al. Among authors: kuhlenbaumer g. Int J Stroke. 2023 Jul;18(6):728-735. doi: 10.1177/17474930231152124. Epub 2023 Feb 1. Int J Stroke. 2023. PMID: 36622021

2

Negative ultrasound findings in patients with cervical artery dissection. Negative ultrasound in CAD.

Dittrich R, Dziewas R, Ritter MA, Kloska SP, Bachmann R, Nassenstein I, Kuhlenbaumer G, Heindel W, Ringelstein EB, Nabavi DG. Dittrich R, et al. Among authors: kuhlenbaumer g. J Neurol. 2006 Apr;253(4):424-33. doi: 10.1007/s00415-005-0051-5. Epub 2005 Nov 24. J Neurol. 2006. PMID: 16307203

3

The collagen 1A2 polymorphism rs42524, which is associated with intracranial aneurysms, shows no association with spontaneous cervical artery dissection (sCAD).

Kuhlenbäumer G, Konrad C, Krämer S, Kis B, Nabavi D, Dittrich R, Ringelstein EB. Kuhlenbäumer G, et al. J Neurol Neurosurg Psychiatry. 2006 Jan;77(1):124-5. doi: 10.1136/jnnp.2005.065847. J Neurol Neurosurg Psychiatry. 2006. PMID: 16361613 Free PMC article. No abstract available.

4

Aberrations of dermal connective tissue in patients with cervical artery dissection (sCAD).

Uhlig P, Bruckner P, Dittrich R, Ringelstein EB, Kuhlenbäumer G, Hansen U. Uhlig P, et al. Among authors: kuhlenbaumer g. J Neurol. 2008 Mar;255(3):340-6. doi: 10.1007/s00415-008-0585-4. Epub 2008 Mar 14. J Neurol. 2008. PMID: 18338201

5

Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3.

Liehr T, Kuhlenbäumer G, Wulf P, Taylor V, Suter U, Van Broeckhoven C, Lupski JR, Claussen U, Rautenstrauss B. Liehr T, et al. Among authors: kuhlenbaumer g. Genomics. 1999 May 15;58(1):106-8. doi: 10.1006/geno.1999.5803. Genomics. 1999. PMID: 10331954 No abstract available.

6

Novel septin 9 repeat motifs altered in neuralgic amyotrophy bind and bundle microtubules.

Bai X, Bowen JR, Knox TK, Zhou K, Pendziwiat M, Kuhlenbäumer G, Sindelar CV, Spiliotis ET. Bai X, et al. Among authors: kuhlenbaumer g. J Cell Biol. 2013 Dec 23;203(6):895-905. doi: 10.1083/jcb.201308068. J Cell Biol. 2013. PMID: 24344182 Free PMC article.

7

Structure of the gene encoding the rat T cell ecto-ADP-ribosyltransferase RT6.

Haag FA, Kuhlenbäumer G, Koch-Nolte F, Wingender E, Thiele HG. Haag FA, et al. Among authors: kuhlenbaumer g. J Immunol. 1996 Sep 1;157(5):2022-30. J Immunol. 1996. PMID: 8757323

8

Neither collagen 8A1 nor 8A2 mutations play a major role in cervical artery dissection. A mutation analysis and linkage study.

Kuhlenbäumer G, Müller US, Besselmann M, Rauterberg J, Robenek H, Hünermund G, Brandt T, Ringelstein EB, Stögbauer F, Hausser I. Kuhlenbäumer G, et al. J Neurol. 2004 Mar;251(3):357-9. doi: 10.1007/s00415-004-0335-1. J Neurol. 2004. PMID: 15015022 No abstract available.

9

Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous.

Kuhlenbäumer G, Meuleman J, De Jonghe P, Falck B, Young P, Hünermund G, Van Broeckhoven C, Timmerman V, Stögbauer F. Kuhlenbäumer G, et al. J Neurol. 2001 Oct;248(10):861-5. doi: 10.1007/s004150170070. J Neurol. 2001. PMID: 11697522

10

[Hereditary neural amyotrophy (HNA): clinical and molecular genetic basis].

Stögbauer F, Young P, Kuhlenbäumer G, Meuleman J, Timmerman V, van Broeckhoven C, Kurlemann G, Ringelstein EB. Stögbauer F, et al. Among authors: kuhlenbaumer g. Fortschr Neurol Psychiatr. 1998 Jan;66(1):10-4. doi: 10.1055/s-2007-995234. Fortschr Neurol Psychiatr. 1998. PMID: 9530552 German.

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