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au.\*:("VAN ENGELEN, B. G. M")

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Clinical neurophysiology of fatigueZWARTS, M. J; BLEIJENBERG, G; VAN ENGELEN, B. G. M et al.Clinical neurophysiology. 2008, Vol 119, Num 1, pp 2-10, issn 1388-2457, 9 p.Article

Possible mechanisms of muscle cramp from temporal and spatial surface EMG characteristicsROELEVELD, K; VAN ENGELEN, B. G. M; STEGEMAN, D. F et al.Journal of applied physiology (1985). 2000, Vol 88, Num 5, pp 1698-1706, issn 8750-7587Article

Warming up improves speech production in patients with adult onset myotonic dystrophyDE SWART, B. J. M; VAN ENGELEN, B. G. M; MAASSEN, B. A. M et al.Journal of communication disorders. 2007, Vol 40, Num 3, pp 185-195, issn 0021-9924, 11 p.Article

Strong association between myotonic dystrophy type 2 and autoimmune diseasesTIELEMAN, A. A; DEN BROEDER, A. A; VAN DE LOGT, A.-E et al.Journal of neurology, neurosurgery and psychiatry. 2009, Vol 80, Num 11, pp 1293-1295, issn 0022-3050, 3 p.Article

Anti-signal recognition particle autoantibodies : marker of a necrotising myopathyHENGSTMAN, G. J. D; TER LAAK, H. J; VREE EGBERTS, W. T. M et al.Annals of the rheumatic diseases. 2006, Vol 65, Num 12, pp 1635-1638, issn 0003-4967, 4 p.Article

The epidemiology of the Lambert-Eaton myasthenic syndrome in the NetherlandsWIRTZ, P. W; VAN DIJK, J. G; WINTZEN, A. R et al.Neurology. 2004, Vol 63, Num 2, pp 397-398, issn 0028-3878, 2 p.Article

Myotonia and flaccid dysarthria in patients with adult onset myotonic dystrophyDE SWART, B. J. M; VAN ENGELEN, B. G. M; VAN DE KERKHOF, J. P. B. M et al.Journal of neurology, neurosurgery and psychiatry. 2004, Vol 75, Num 10, pp 1480-1482, issn 0022-3050, 3 p.Article

A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesionsGOMMANS, I. M. P; DAVIS, M; LAING, N et al.Brain. 2003, Vol 126, pp 1545-1551, issn 0006-8950, 7 p., 7Article

Propagation disturbance of motor unit action potentials during transient paresis in generalized myotonia: A high-density surface EMG studyDROST, G; BLOK, J. H; STEGEMAN, D. F et al.Brain. 2001, Vol 124, pp 352-360, issn 0006-8950, 2Article

Congenital fibre type disproportion a time-locked diagnosis : A clinical and morphological follow-up studyBARTHOLOMEUS, M. G. T; GABREËLS, F. J. M; TER LAAK, H. J et al.Clinical neurology and neurosurgery. 2000, Vol 102, Num 2, pp 97-101, issn 0303-8467Article

Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth diseaseGABREËLS-FESTEN, A. A. W. M; HOOGENDIJK, J. E; VAN ENGELEN, B. G. M et al.Neurology. 1996, Vol 47, Num 3, pp 761-765, issn 0028-3878Article

Ocular and systemic manifestations of cerebrotendinous xanthomatosisCRUYSBERG, J. R. M; WEVERS, R. A; VAN ENGELEN, B. G. M et al.American journal of ophthalmology. 1995, Vol 120, Num 5, pp 597-604, issn 0002-9394Article

A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndromeDE VRIES, D. D; VAN ENGELEN, B. G. M; GABREËLS, F. J. M et al.Annals of neurology. 1993, Vol 34, Num 3, pp 410-412, issn 0364-5134Conference Paper

Clinical features of facioscapulohumeral muscular dystrophy 2DE GREEF, J. C; LEMMERS, R. J. L. F; DESNUELLE, C et al.Neurology. 2010, Vol 75, Num 17, pp 1548-1554, issn 0028-3878, 7 p.Article

Redefining the clinical phenotypes of non-dystrophic myotonic syndromesTRIP, J; DROST, G; GINJAAR, H. B et al.Journal of neurology, neurosurgery and psychiatry. 2009, Vol 80, Num 6, pp 647-652, issn 0022-3050, 6 p.Article

Ptosis as a feature of late-onset glycogenosis type IIGROEN, W. B; LEEN, W. G; VOS, A. M. C et al.Neurology. 2006, Vol 67, Num 12, pp 2261-2262, issn 0028-3878, 2 p.Article

Ptosis aggravates dysphagia in oculopharyngeal muscular dystrophyDE SWART, B. J. M; VAN DER SLUIJS, B. M; VOS, A. M. C et al.Journal of neurology, neurosurgery and psychiatry. 2006, Vol 77, Num 2, pp 266-268, issn 0022-3050, 3 p.Article

Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entityVON DER SLUIJS, B. M; TER LAAK, H. J; SCHEFFER, H et al.Journal of neurology, neurosurgery and psychiatry. 2004, Vol 75, Num 10, pp 1499-1501, issn 0022-3050, 3 p.Article

Clinical and serological characteristics of 125 Dutch myositis patients: Myositis specific autoantibodies aid in the differential diagnosis of the idiopathic inflammatory myopathiesHENGSTMAN, G. J. D; BROUWER, R; EGBERTS, W. T. M. Vree et al.Journal of neurology. 2002, Vol 249, Num 1, pp 69-75, issn 0340-5354Article

Muscle function during repetitive moderate-intensity muscle contractions in myoadenylate deaminase-deficient Dutch subjectsDE RUITER, C. J; MAY, A. M; VAN ENGELEN, B. G. M et al.Clinical science (1979). 2002, Vol 102, Num 5, pp 531-539, issn 0143-5221Article

Difference in distribution of muscle weakness between myasthenia gravis and the Lambert-Eaton myasthenic syndromeWIRTZ, P. W; SOTODEH, M; VISSER, L. H et al.Journal of neurology, neurosurgery and psychiatry. 2002, Vol 73, Num 6, pp 766-768, issn 0022-3050, 3 p.Article

Scheie syndrome presenting as myopathyVERRIPS, A; VAN ENGELEN, B. G. M; TER LAAK, H et al.Neuropediatrics. 2001, Vol 32, Num 2, pp 93-96, issn 0174-304XArticle

Leukoencephalopathy with swelling in children and adolescents : MRI patterns and differential diagnosisVAN DER KNAAP, M. S; VALK, J; BARTH, P. G et al.Neuroradiology (Berlin. Print). 1995, Vol 37, Num 8, pp 679-686, issn 0028-3940Article

Cerebrospinal fluid examinations in cryptogenic West and Lennox-Gastaut syndrome before and after intravenous immunoglobulin administrationVAN ENGELEN, B. G. M; RENIER, W. O; WEEMAES, C. M. R et al.Epilepsy research. 1994, Vol 18, Num 2, pp 139-147, issn 0920-1211Article

Evaluation of prednisolone treatment in the acute phase of neuralgic amyotrophy: an observational studyVAN EIJK, J. J. J; VAN ALFEN, N; BERREVOETS, M et al.Journal of neurology, neurosurgery and psychiatry. 2009, Vol 80, Num 10, pp 1120-1124, issn 0022-3050, 5 p.Article

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