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566 results

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Page 1
Recurrent neuropathy associated with Ehlers-Danlos syndrome.
Voermans NC, Drost G, van Kampen A, Gabreëls-Festen AA, Lammens M, Hamel BC, Schalkwijk J, van Engelen BG. Voermans NC, et al. Among authors: van kampen a, van engelen bg. J Neurol. 2006 May;253(5):670-1. doi: 10.1007/s00415-005-0056-0. Epub 2005 Nov 29. J Neurol. 2006. PMID: 16311893 No abstract available.
Familial adult-onset muscular dystrophy with leukoencephalopathy.
van Engelen BG, Leyten QH, Bernsen PL, Gabreëls FJ, Barkhof F, Joosten EM, Hamel BC, ter Laak HJ, Ruijs MB, Cruysberg JR, et al. van Engelen BG, et al. Ann Neurol. 1992 Oct;32(4):577-80. doi: 10.1002/ana.410320415. Ann Neurol. 1992. PMID: 1456743
Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease.
Gabreëls-Festen AA, Hoogendijk JE, Meijerink PH, Gabreëls FJ, Bolhuis PA, van Beersum S, Kulkens T, Nelis E, Jennekens FG, de Visser M, van Engelen BG, Van Broeckhoven C, Mariman EC. Gabreëls-Festen AA, et al. Among authors: van beersum s, van engelen bg, van broeckhoven c. Neurology. 1996 Sep;47(3):761-5. doi: 10.1212/wnl.47.3.761. Neurology. 1996. PMID: 8797476
Differences between hereditary motor and sensory neuropathy type 2 and chronic idiopathic axonal neuropathy. A clinical and electrophysiological study.
Teunissen LL, Notermans NC, Franssen H, van der Graaf Y, Oey PL, Linssen WH, van Engelen BG, Ippel PF, van Dijk GW, Gabreëls-Festen AA, Wokke JH. Teunissen LL, et al. Among authors: van der graaf y, van dijk gw, van engelen bg. Brain. 1997 Jun;120 ( Pt 6):955-62. doi: 10.1093/brain/120.6.955. Brain. 1997. PMID: 9217680
Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation.
Lenssen PP, Gabreëls-Festen AA, Valentijn LJ, Jongen PJ, van Beersum SE, van Engelen BG, van Wensen PJ, Bolhuis PA, Gabreëls FJ, Mariman EC. Lenssen PP, et al. Among authors: van beersum se, van wensen pj, van engelen bg. Brain. 1998 Aug;121 ( Pt 8):1451-8. doi: 10.1093/brain/121.8.1451. Brain. 1998. PMID: 9712007
Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.
Gabreëls-Festen A, van Beersum S, Eshuis L, LeGuern E, Gabreëls F, van Engelen B, Mariman E. Gabreëls-Festen A, et al. J Neurol Neurosurg Psychiatry. 1999 May;66(5):569-74. doi: 10.1136/jnnp.66.5.569. J Neurol Neurosurg Psychiatry. 1999. PMID: 10209165 Free PMC article.
Abeta fibers mediate cutaneous reflexes during human walking.
van Wezel BM, van Engelen BG, Gabreëls FJ, Gabreëls-Festen AA, Duysens J. van Wezel BM, et al. Among authors: van engelen bg. J Neurophysiol. 2000 May;83(5):2980-6. doi: 10.1152/jn.2000.83.5.2980. J Neurophysiol. 2000. PMID: 10805693 Free article. Clinical Trial.
566 results