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[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: young p. Fortschr Neurol Psychiatr. 1998 Jan;66(1):10-4. doi: 10.1055/s-2007-995234. Fortschr Neurol Psychiatr. 1998. PMID: 9530552 German.
Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 gene.
Stögbauer F, Young P, Kerschensteiner M, Ringelstein EB, Assmann G, Funke H. Stögbauer F, et al. Among authors: young p. Muscle Nerve. 1998 Sep;21(9):1199-201. doi: 10.1002/(sici)1097-4598(199809)21:9<1199::aid-mus12>3.0.co;2-n. Muscle Nerve. 1998. PMID: 9703447
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. Among authors: young p. J Neurol. 2001 Oct;248(10):861-5. doi: 10.1007/s004150170070. J Neurol. 2001. PMID: 11697522
3,582 results