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Results: 1-15 |
Results: 15
Basal metabolic rate in children with a solid tumour
Authors: den Broeder, E Oeseburg, B Lippens, RJJ van Staveren, WA Sengers, RCA van't Hof, MA Tolboom, JJM
Citation: E. Den Broeder et al., Basal metabolic rate in children with a solid tumour, EUR J CL N, 55(8), 2001, pp. 673-681
Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial
Authors: Noordam, C van der Burgt, I Sengers, RCA Delemarre-van de Waal, HA Otten, BJ
Citation: C. Noordam et al., Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial, ACT PAEDIAT, 90(8), 2001, pp. 889-894
Growth hormone (GH) secretion in children with Noonan syndrome: frequentlyabnormal without consequences for growth or response to GH treatment
Authors: Noordam, C van der Burgt, I Sweep, CGJ Delemarre-van de Waal, HA Sengers, RCA Otten, BJ
Citation: C. Noordam et al., Growth hormone (GH) secretion in children with Noonan syndrome: frequentlyabnormal without consequences for growth or response to GH treatment, CLIN ENDOCR, 54(1), 2001, pp. 53-59
Prenatal diagnosis of NADH : ubiquinone oxidoreductase deficiency
Authors: Niers, LEM Smeitink, JAM Trijbels, JMF Sengers, RCA Janssen, AJM van den Heuvel, LP
Citation: Lem. Niers et al., Prenatal diagnosis of NADH : ubiquinone oxidoreductase deficiency, PRENAT DIAG, 21(10), 2001, pp. 871-880
Infantile presentation of the mtDNA A3243G tRNA(Leu(UUR)) mutation
Authors: Okhuijsen-Kroes, EJ Trijbels, JMF Sengers, RCA Mariman, E van den Heuvel, LP Wendel, U Koch, G Smeitink, JAM
Citation: Ej. Okhuijsen-kroes et al., Infantile presentation of the mtDNA A3243G tRNA(Leu(UUR)) mutation, NEUROPEDIAT, 32(4), 2001, pp. 183-190
Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith-Lemli-Opitz syndrome
Authors: Jira, PE Wanders, RJA Smeitink, JAM De Jong, J Wevers, RA Oostheim, W Tuerlings, JHAM Hennekam, RCM Sengers, RCA Waterham, HR
Citation: Pe. Jira et al., Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith-Lemli-Opitz syndrome, ANN HUM GEN, 65, 2001, pp. 229-236
Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutations
Authors: Rubio-Gozalbo, ME Dijkman, KP van den Heuvel, LP Sengers, RCA Wendel, U Smeitink, JAM
Citation: Me. Rubio-gozalbo et al., Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutations, HUM MUTAT, 15(6), 2000, pp. 522-532
Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects
Authors: Loeffen, JLCM Smeitink, JAM Trijbels, JMF Janssen, AJM Triepels, RH Sengers, RCA van den Heuvel, LP
Citation: Jlcm. Loeffen et al., Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects, HUM MUTAT, 15(2), 2000, pp. 123-134
Association between the change in nutritional status in response to tube feeding and the occurrence of infections in children with a solid tumor
Authors: den Broeder, E Lippens, RJJ van't Hof, MA Tolboom, JJM Sengers, RCA van Staveren, WA
Citation: E. Den Broeder et al., Association between the change in nutritional status in response to tube feeding and the occurrence of infections in children with a solid tumor, PED HEM ONC, 17(7), 2000, pp. 567-575
Nuclear genes and oxidative phosphorylation disorders: a review
Authors: Smeitink, JAM Sengers, RCA Trijbels, FJM van den Heuvel, LP
Citation: Jam. Smeitink et al., Nuclear genes and oxidative phosphorylation disorders: a review, EUR J PED, 159, 2000, pp. S227-S231
A prognostic index as diagnostic strategy in children suspected of mitochondriocytopathy
Authors: Rubio-Gozalbo, ME Sengers, RCA Trijbels, JMF Doesburg, WH Janssen, AJM Verbeek, ALM Smeitink, JAM
Citation: Me. Rubio-gozalbo et al., A prognostic index as diagnostic strategy in children suspected of mitochondriocytopathy, NEUROPEDIAT, 31(3), 2000, pp. 114-121
Nasogastric tube feeding in children with cancer: The effect of two different formulas on weight, body composition, and serum protein concentrations
Authors: den Broeder, E Lippens, RJJ van't Hof, MA Tolboom, JJM Sengers, RCA van den Berg, AMJ van Houdt, NBM Hofman, Z van Staveren, WA
Citation: E. Den Broeder et al., Nasogastric tube feeding in children with cancer: The effect of two different formulas on weight, body composition, and serum protein concentrations, J PARENT EN, 24(6), 2000, pp. 351-360
Simvastatin: a new therapeutic approach for Smith-Lemli-Opitz syndrome
Authors: Jira, PE Wevers, RA de Jong, J Rubio-Gozalbo, E Janssen-Zijlstra, FSM van Heyst, AFJ Sengers, RCA Smeitink, JAM
Citation: Pe. Jira et al., Simvastatin: a new therapeutic approach for Smith-Lemli-Opitz syndrome, J LIPID RES, 41(8), 2000, pp. 1339-1346
Preterm birth in Sjogren-Larsson syndrome
Authors: Willemsen, MAAP Rotteveel, JJ van Domburg, PHMF Gabreels, FJM Mayatepek, E Sengers, RCA
Citation: Maap. Willemsen et al., Preterm birth in Sjogren-Larsson syndrome, NEUROPEDIAT, 30(6), 1999, pp. 325-327
Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency
Authors: Rubio-Gozalbo, ME Smeitink, JAM Ruitenbeek, W Ter Laak, H Mullaart, RA Schuelke, M Mariman, ECM Sengers, RCA Gabreels, FJM
Citation: Me. Rubio-gozalbo et al., Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency, NEUROLOGY, 52(2), 1999, pp. 383-386
Risultati: 1-15 |