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Results 1 to 25 of 48

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Why cells die in faciocapulohumeral muscular dystrophyPADBERG, G. W.Clinical neurology and neurosurgery. 1992, Vol 94, pp S21-S24, issn 0303-8467, SUPConference Paper

Limb-girdle muscular dystrophy in the Netherlands : Gene defect identified in half the familiesVAN DER KOOI, A. J; FRANKHUIZEN, W. S; BAKKER, E et al.Neurology. 2007, Vol 68, Num 24, pp 2125-2128, issn 0028-3878, 4 p.Article

The neuropathology of hereditary congenital facial palsy vs Möbius syndromeVERZIJL, H. T. F. M; VAN DER ZWAAG, B; LAMMENS, M et al.Neurology. 2005, Vol 64, Num 4, pp 649-653, issn 0028-3878, 5 p.Article

Strength training and albuterol in facioscapulohumeral muscular dystrophyVAN DER KOOI, E. L; VOGELS, O. J. M; VAN ASSELDONK, R. J. G. P et al.Neurology. 2004, Vol 63, Num 4, pp 702-708, issn 0028-3878, 7 p.Article

FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patientsRIJKERS, T; DEIDDA, G; VAN DER MAAREL, S. M et al.Journal of medical genetics. 2004, Vol 41, Num 11, pp 826-836, issn 0022-2593, 11 p.Article

Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472ENSINK, R. J. H; VERHOEVEN, K; MARRES, H. A. M et al.Archives of otolaryngology, head & neck surgery. 1998, Vol 124, Num 8, pp 886-891, issn 0886-4470Article

Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomasMARSH, D. J; ZHENG, Z; ZEDENIUS, J et al.Cancer research (Baltimore). 1997, Vol 57, Num 3, pp 500-503, issn 0008-5472Article

Mutation in DHP receptor α1 subunit (CALCLN1A3) gene in a Dutch family with hypokalaemic periodic paralysisBOERMAN, R. H; OPHOFF, R. A; FONTAINE, B et al.Journal of medical genetics. 1995, Vol 32, Num 1, pp 44-47, issn 0022-2593Article

Facioscapulohumeral muscular dystrophy in early childhoodBROUWER, O. F; PADBERG, G. W; WIJMENGA, C et al.Archives of neurology (Chicago). 1994, Vol 51, Num 4, pp 387-394, issn 0003-9942Article

Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHDDE GREEF, J. C; WOHLGEMUTH, M; CHAN, O. A et al.Neurology. 2007, Vol 69, Num 10, pp 1018-1026, issn 0028-3878, 9 p.Article

Localization of the gene for Cowden disease to chromosome 10q22-23NELEN, M. R; PADBERG, G. W; EELES, R. A et al.Nature genetics. 1996, Vol 13, Num 1, pp 114-116, issn 1061-4036Article

Molecular genetic reevaluation of the dutch hyperkpexlia familyTIJSSEN, M. A. J; RITA SHIANG; VAN DEUTEKOM, J et al.Archives of neurology (Chicago). 1995, Vol 52, Num 6, pp 578-582, issn 0003-9942Article

Facioscapulohumeral muscular dystrophy in the dutch populationPADBERG, G. W; FRANTS, R. R; BROUWER, O. F et al.Muscle & nerve. 1995, pp S81-S84, issn 0148-639X, SUP2Conference Paper

Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35VAN DEUTEKOM, J. C. T; HOFKER, M. H; ROMBERG, S et al.Muscle & nerve. 1995, pp S19-S26, issn 0148-639X, SUP2Conference Paper

Facioscapulohumeral muscular dystrophy: the impact of genetic researchBROUWER, O. F; WIJMENGA, C; FRANTS, R. R et al.Clinical neurology and neurosurgery. 1993, Vol 95, Num 1, pp 9-21, issn 0303-8467Article

Treatment of single brain metastasis : radiotherapy alone or combined with neurosurgery ?VECHT, C. J; HAAXMA-REICHE, H; BRAND, R et al.Annals of neurology. 1993, Vol 33, Num 6, pp 583-590, issn 0364-5134Article

Adult adrenoleukodystrophy : the clinical spectrum in a large Dutch familyZWETSLOOT, C. P; PADBERG, G. W; VAN SETERS, A. P et al.Journal of neurology. 1992, Vol 239, Num 2, pp 107-111, issn 0340-5354Article

Transmission of de-novo mutation associated with facioscapulohumeral muscular dystrophyWIJMENGA, C; BROUWER, O. F; PADBERG, G. W et al.Lancet (British edition). 1992, Vol 340, Num 8825, pp 985-986, issn 0140-6736Article

Hearing loss in facioscapulohumeral muscular dystrophyBROUWER, O. F; PADBERG, G. W; RUYS, C. J. M et al.Neurology. 1991, Vol 41, Num 12, pp 1878-1881, issn 0028-3878Article

Syncope or seizure ? The diagnostic value of the EEG and hyperventilation test in transient loss of consciousnessHOEFNAGELS, W. A. J; PADBERG, G. W; OVERWEG, J et al.Journal of neurology, neurosurgery and psychiatry. 1991, Vol 54, Num 11, pp 953-956, issn 0022-3050Conference Paper

Effects of training and albuterol on pain and fatigue in facioscapulohumeral muscular dystrophyVAN DER KOOI, E. L; KALKMAN, J. S; LINDEMAN, E et al.Journal of neurology. 2007, Vol 254, Num 7, pp 931-940, issn 0340-5354, 10 p.Article

Ventilatory support in facioscapulohumeral muscular dystrophyWOHLGEMUTH, M; VAN DER KOOI, E. L; VAN KESTEREN, R. G et al.Neurology. 2004, Vol 63, Num 1, pp 176-178, issn 0028-3878, 3 p.Article

D4F104S1 deletion in facioscapulohumeral muscular dystrophy: Phenotype, size, and detectionLEMMERS, R. J. L. F; OSBORN, M; HAAF, T et al.Neurology. 2003, Vol 61, Num 2, pp 178-183, issn 0028-3878, 6 p.Article

Genetic characteristics of myoadenylate deaminase deficiencyVERZIJL, H. T. F. M; VAN ENGELEN, B. G. M; LUYTEN, J. A. F. M et al.Annals of neurology. 1998, Vol 44, Num 1, pp 140-143, issn 0364-5134Article

Early onset facioscapulohumeral muscular dystrophyBROUWER, O. F; PADBERG, G. W; BAKKER, E et al.Muscle & nerve. 1995, pp S67-S72, issn 0148-639X, SUP2Conference Paper

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