au.\*:("SENGERS, R. C. A")
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Effects of rapid versus slow infusion of sodium bicarbonate on cerebral hemodynamics and oxygenation in preterm infantsVAN ALFEN-VAN DER VELDEN, A. A. E. M; HOPMAN, J. C. W; KLAESSENS, J. H. G. M et al.Biology of the neonate. 2006, Vol 90, Num 2, pp 122-127, issn 0006-3126, 6 p.Article
Smith-Lemli-Opitz syndrome and the DHCR7 geneJIRA, P. E; WATERHAM, H. R; WANDERS, R. J. A et al.Annals of human genetics. 2003, Vol 67, Num 3, pp 269-280, issn 0003-4800, 12 p.Article
Systemic infantile complex I deficiency with fatal outcome in two brothersRUBIO-GOZALBO, M. E; RUITENBEEK, W; WENDEL, U et al.Neuropediatrics. 1998, Vol 29, Num 1, pp 43-45, issn 0174-304XArticle
White matter abnormalities in congenital muscular dystrophyLEYTEN, Q. H; GABREËLS, F. J. M; RENIER, W. O et al.Journal of the neurological sciences. 1995, Vol 129, Num 2, pp 162-169, issn 0022-510XArticle
Impaired prenatal and postnatal growth in Dutch patients with phenylketonuriaVERKERK, P. H; VAN SPRONSEN, F. J; SMIT, G. P. A et al.Archives of disease in childhood. 1994, Vol 71, Num 2, pp 114-118, issn 0003-9888Article
Deficiency of the adenine nucleotide translocator in muscle of a patient with myopathy and lactic acidosis : a new mitochondrial defectBAKKER, H. D; SCHOLTE, H. R; VAN DEN BOGERT, C et al.Pediatric research. 1993, Vol 33, Num 4, pp 412-417, issn 0031-3998, 1Article
Differentiation of human skeletal muscle cells in culture : maturation as indicated by titin and desmin striationVAN DER VEN, P. F. M; SCHAART, G; JAP, P. H. K et al.Cell and tissue research. 1992, Vol 270, Num 1, pp 189-198, issn 0302-766XArticle
High-resolution physical mapping of four microsatellite repeat markers near the RYR1 locus on chromosome 19q13.1 and apparent exclusion of the MHS locus from this region in two malignant hyperthermia susceptible familiesILES, D. E; SEGERS, B; HEYTENS, L et al.Genomics (San Diego, Calif.). 1992, Vol 14, Num 3, pp 749-754, issn 0888-7543Article
The use of chorionic villi in prenatal diagnosis of mitochondriopathiesRUITENBEEK, W; SENGERS, R. C. A; TRIJBELS, J. M. F et al.Journal of inherited metabolic disease. 1992, Vol 15, Num 3, pp 303-306, issn 0141-8955Conference Paper
Congenital muscular dystrophyLEYTEN, Q. H; GABREELS, F. J. M; RENIER, W. O et al.The Journal of pediatrics. 1989, Vol 115, Num 2, pp 214-221, issn 0022-3476, 8 p.Article
Features of a syndrome with congenital cataract and hypertrophic cardiomyopathyCRUYSBERG, J. R. M; SENGERS, R. C. A; PINCKERS, A et al.American journal of ophthalmology. 1986, Vol 102, Num 6, pp 740-749, issn 0002-9394Article
Effects of midazolam and morphine on cerebral oxygenation and hemodynamics in ventilated premature infantsVAN ALFEN-VAN DER VELDEN, A. A. E. M; HOPMAN, J. C. W; KLAESSENS, J. H. G. M et al.Biology of the neonate. 2006, Vol 90, Num 3, pp 197-202, issn 0006-3126, 6 p.Article
Prenatal diagnosis of NADH:ubiquinone oxidoreductase deficiencyNIERS, L. E. M; SMEITINK, J. A. M; TRIJBELS, J. M. F et al.Prenatal diagnosis. 2001, Vol 21, Num 10, pp 871-880, issn 0197-3851Article
A prognostic index as diagnostic strategy in children suspected of mitochondriocytopathyRUBIO-GOZALBO, M. E; SENGERS, R. C. A; TRIJBELS, J. M. F et al.Neuropediatrics. 2000, Vol 31, Num 3, pp 114-121, issn 0174-304XArticle
Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiencyRUBIO-GOZALBO, M. E; SMEITINK, J. A. M; RUITENBEEK, W et al.Neurology. 1999, Vol 52, Num 2, pp 383-386, issn 0028-3878Article
Preterm birth in Sjögren-Larsson syndromeWILLEMSEN, M. A. A. P; ROTTEVEEL, J. J; VAN DOMBURG, P. H. M. F et al.Neuropediatrics. 1999, Vol 30, Num 6, pp 325-327, issn 0174-304XArticle
Congenital muscular dystrophy : a study on the variability of morphological changes and dystrophin distribution in muscle biopsiesLEYTEN, Q. H; TER LAAK, H. J; GABREËLS, F. J. M et al.Acta neuropathologica. 1993, Vol 86, Num 4, pp 386-392, issn 0001-6322Article
Lipid peroxidation in homocysteinaemiaBLOM, H. J; ENGELEN, D. P. E; BOERS, G. H. J et al.Journal of inherited metabolic disease. 1992, Vol 15, Num 3, pp 419-422, issn 0141-8955Conference Paper
In vitro contraction tes for malignant hyperthermia in patients with unexplained recurrent rhabdomyolysisPOELS, P. J. E; JOOSTEN, E. M. G; SENGERS, R. C. A et al.Journal of the neurological sciences. 1991, Vol 105, Num 1, pp 67-72, issn 0022-510XArticle
Increased volume density of peripheral motochondria in skeletal muscle of children with exercise intoleranceVAN EKEREN, G. J; CORNELISSEN, E. A. M; STADHOUDERS, A. M et al.European journal of pediatrics. 1991, Vol 150, Num 10, pp 744-750, issn 0340-6199Article
Detection of respiratory chain dysfunction by measuring lactate and pyruvate production in cultured fibroblastsWIJBURG, F. A; FELLER, N; RUITENBEEK, W et al.Journal of inherited metabolic disease. 1990, Vol 13, Num 3, pp 355-358, issn 0141-8955, 4 p.Article
GMi2-Gangliosidosis : clinical and biochemical aspects of four casesPRAAMSTRA, P; WEVERS, R. A; GABREELS, F. J. M et al.Clinical neurology and neurosurgery. 1990, Vol 92, Num 2, pp 143-148, issn 0303-8467, 6 p.Article
Heterogeneous tissue expression of enzyme defects in mitochondrial myopathiesSPERL, W; RUITENBEEK, W; TRIJBELS, J. M. F et al.Journal of inherited metabolic disease. 1990, Vol 13, Num 3, pp 359-362, issn 0141-8955, 4 p.Article
Computerized calculation of in vitro generation of ATP and creatine phosphate induced by respiration in human muscle mitochondriaFISCHER, J. C; RUITENBEEK, W; STADHOUDERS, A. M et al.Computers in biology and medicine. 1985, Vol 15, Num 5, pp 269-277, issn 0010-4825Article
Investigation of mitochondrial metabolism in small human skeletal muscle biopsy specimens. Improvement of preparation procedureFISCHER, J. C; RUITENBEEK, W; STADHOUDERS, A. M et al.Clinica chimica acta. 1985, Vol 145, Num 1, pp 89-99, issn 0009-8981Article