Spoelders P - Search Results

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Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.

De Jonghe P, Timmerman V, FitzPatrick D, Spoelders P, Martin JJ, Van Broeckhoven C. De Jonghe P, et al. Among authors: spoelders p. J Neurol Neurosurg Psychiatry. 1997 Jun;62(6):570-3. doi: 10.1136/jnnp.62.6.570. J Neurol Neurosurg Psychiatry. 1997. PMID: 9219740 Free PMC article.

Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13.

Timmerman V, De Jonghe P, Spoelders P, Simokovic S, Löfgren A, Nelis E, Vance J, Martin JJ, Van Broeckhoven C. Timmerman V, et al. Among authors: spoelders p. Neurology. 1996 May;46(5):1311-8. doi: 10.1212/wnl.46.5.1311. Neurology. 1996. PMID: 8628473

Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17q.

Wehnert M, Timmerman V, Spoelders P, Meuleman J, Nelis E, Van Broeckhoven C. Wehnert M, et al. Among authors: spoelders p. Neurology. 1997 Jun;48(6):1719-21. doi: 10.1212/wnl.48.6.1719. Neurology. 1997. PMID: 9191796

Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25.

Stögbauer F, Young P, Timmerman V, Spoelders P, Ringelstein EB, Van Broeckhoven C, Kurlemann G. Stögbauer F, et al. Among authors: spoelders p. Hum Genet. 1997 May;99(5):685-7. doi: 10.1007/s004390050430. Hum Genet. 1997. PMID: 9150742

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