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Poor sleep quality and fatigue but no excessive daytime sleepiness in myotonic dystrophy type 2.
Tieleman AA, Knoop H, van de Logt AE, Bleijenberg G, van Engelen BG, Overeem S. Tieleman AA, et al. Among authors: van de logt ae, van engelen bg. J Neurol Neurosurg Psychiatry. 2010 Sep;81(9):963-7. doi: 10.1136/jnnp.2009.192591. J Neurol Neurosurg Psychiatry. 2010. PMID: 20798200
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
Immunoglobulin treatment in human and experimental epilepsy.
van Engelen BG, Renier WO, Weemaes CM. van Engelen BG, et al. J Neurol Neurosurg Psychiatry. 1994 Nov;57 Suppl(Suppl):72-5. doi: 10.1136/jnnp.57.suppl.72. J Neurol Neurosurg Psychiatry. 1994. PMID: 7964861 Free PMC article. Review.
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 engelen bg, van oost ba. 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.
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 engelen bg, van wensen pj. 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. Among authors: van beersum s, van engelen b. 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.
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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