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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: 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.
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.
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