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431 results
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A weak balance: the contribution of muscle weakness to postural instability and falls.
Horlings CG, van Engelen BG, Allum JH, Bloem BR. Horlings CG, et al. Among authors: van engelen bg. Nat Clin Pract Neurol. 2008 Sep;4(9):504-15. doi: 10.1038/ncpneuro0886. Nat Clin Pract Neurol. 2008. PMID: 18711425 Review.
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
A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome.
de Vries DD, van Engelen BG, Gabreëls FJ, Ruitenbeek W, van Oost BA. de Vries DD, et al. Among authors: van oost ba, van engelen bg. Ann Neurol. 1993 Sep;34(3):410-2. doi: 10.1002/ana.410340319. Ann Neurol. 1993. PMID: 8395787
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
Lumbosacral plexus neuropathy: a case report and review of the literature.
van Alfen N, van Engelen BG. van Alfen N, et al. Among authors: van engelen bg. Clin Neurol Neurosurg. 1997 May;99(2):138-41. doi: 10.1016/s0303-8467(97)00603-3. Clin Neurol Neurosurg. 1997. PMID: 9213060 Review.
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
Genetic characteristics of myoadenylate deaminase deficiency.
Verzijl HT, van Engelen BG, Luyten JA, Steenbergen GC, van den Heuvel LP, ter Laak HJ, Padberg GW, Wevers RA. Verzijl HT, et al. Among authors: van engelen bg, van den heuvel lp. Ann Neurol. 1998 Jul;44(1):140-3. doi: 10.1002/ana.410440124. Ann Neurol. 1998. PMID: 9667605 Clinical Trial.
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
Postural changes, dysphagia, and systemic sclerosis.
Barrera P, den Broeder AA, van den Hoogen FH, van Engelen BG, van de Putte LB. Barrera P, et al. Among authors: van de putte lb, van den hoogen fh, van engelen bg. Ann Rheum Dis. 1998 Jun;57(6):331-8. doi: 10.1136/ard.57.6.331. Ann Rheum Dis. 1998. PMID: 9771206 Free PMC article. No abstract available.
Decreased striatal dopamine-receptor binding in sporadic ALS: glutamate hyperactivity?
Vogels OJ, Oyen WJ, van Engelen BG, Padberg GW, Horstink MW. Vogels OJ, et al. Among authors: van engelen bg. Neurology. 1999 Apr 12;52(6):1275-7. doi: 10.1212/wnl.52.6.1275. Neurology. 1999. PMID: 10214758
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