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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
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.
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.
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
PMP22 Thr118Met is not a clinically relevant CMT1 marker.
Young P, Stögbauer F, Eller B, de Jonghe P, Löfgren A, Timmerman V, Rautenstrauss B, Oexle K, Grehl H, Kuhlenbäumer G, Van Broeckhoven C, Ringelstein EB, Funke H. Young P, et al. Among authors: kuhlenbaumer g. J Neurol. 2000 Sep;247(9):696-700. doi: 10.1007/s004150070113. J Neurol. 2000. PMID: 11081809
164 results