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Page 1
[Spontaneous dissection of brain providing neck artery].
Kuhlenbäumer G, Ringelstein EB, Stögbauer F. Kuhlenbäumer G, et al. Fortschr Neurol Psychiatr. 2004 May;72(5):282-91; quiz 292-3. doi: 10.1055/s-2003-812432. Fortschr Neurol Psychiatr. 2004. PMID: 15136949 Review. German. No abstract available.
[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.
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: kuhlenbaumer g. 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.
Hereditary neuralgic amyotrophy: mutation analysis of candidate genes.
Meuleman J, Kuhlenbäumer G, Schirmacher A, Wehnert M, Young P, Stögbauer F, Ringelstein EB, Van Broeckhoven C, Timmerman V. Meuleman J, et al. Among authors: kuhlenbaumer g. Ann N Y Acad Sci. 1999 Sep 14;883:443-4. Ann N Y Acad Sci. 1999. PMID: 10586268 No abstract available.
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. Ann N Y Acad Sci. 1999 Sep 14;883:445-8. Ann N Y Acad Sci. 1999. PMID: 10586269 No abstract available.
Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25.
Meulemann J, Kuhlenbäumer G, Schirmacher A, Wehnert M, De Jonghe P, De Vriendt E, Young P, Airaksinen E, Pou-Serradell A, Prats JM, Ringelstein B, Stögbauer F, Van Broeckhoven C, Timmerman V. Meulemann J, et al. Among authors: kuhlenbaumer g. Eur J Hum Genet. 1999 Dec;7(8):920-7. doi: 10.1038/sj.ejhg.5200384. Eur J Hum Genet. 1999. PMID: 10602368
163 results