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Page 1
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
Mutations in SEPT9 cause hereditary neuralgic amyotrophy.
Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF. Kuhlenbäumer G, et al. Nat Genet. 2005 Oct;37(10):1044-6. doi: 10.1038/ng1649. Epub 2005 Sep 25. Nat Genet. 2005. PMID: 16186812
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.
Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA).
Meuleman J, Kuhlenbäumer G, Audenaert D, Hünermund G, Hor H, Young P, Stögbauer F, Ringelstein EB, Van Broeckhoven C, De Jonghe P, Timmerman V. Meuleman J, et al. Among authors: kuhlenbaumer g. Hum Genet. 2001 May;108(5):390-3. doi: 10.1007/s004390100510. Hum Genet. 2001. PMID: 11409865
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 Oct;883(1):443-444. doi: 10.1111/j.1749-6632.1999.tb08605.x. Ann N Y Acad Sci. 1999. PMID: 29086982 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.
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.
164 results