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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
White matter abnormalities in congenital muscular dystrophy.
Leyten QH, Gabreëls FJ, Renier WO, van Engelen BG, ter Laak HJ, Sengers RC, Thijssen HO. Leyten QH, et al. Among authors: van engelen bg. J Neurol Sci. 1995 Apr;129(2):162-9. doi: 10.1016/0022-510x(94)00264-o. J Neurol Sci. 1995. PMID: 7608731 Free article.
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.
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.
Myositis during long-term interferon-alpha treatment.
Hengstman GJ, Vogels OJ, ter Laak HJ, de Witte T, van Engelen BG. Hengstman GJ, et al. Among authors: van engelen bg. Neurology. 2000 Jun 13;54(11):2186. doi: 10.1212/wnl.54.11.2186. Neurology. 2000. PMID: 10851394 No abstract available.
553 results