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La ricerca find articoli where authors phrase all words ' Sengers, RCA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 41 riferimenti
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    1. den Broeder, E; Oeseburg, B; Lippens, RJJ; van Staveren, WA; Sengers, RCA; van't Hof, MA; Tolboom, JJM
      Basal metabolic rate in children with a solid tumour

      EUROPEAN JOURNAL OF CLINICAL NUTRITION
    2. Noordam, C; van der Burgt, I; Sengers, RCA; Delemarre-van de Waal, HA; Otten, BJ
      Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial

      ACTA PAEDIATRICA
    3. Noordam, C; van der Burgt, I; Sweep, CGJ; Delemarre-van de Waal, HA; Sengers, RCA; Otten, BJ
      Growth hormone (GH) secretion in children with Noonan syndrome: frequentlyabnormal without consequences for growth or response to GH treatment

      CLINICAL ENDOCRINOLOGY
    4. Niers, LEM; Smeitink, JAM; Trijbels, JMF; Sengers, RCA; Janssen, AJM; van den Heuvel, LP
      Prenatal diagnosis of NADH : ubiquinone oxidoreductase deficiency

      PRENATAL DIAGNOSIS
    5. Okhuijsen-Kroes, EJ; Trijbels, JMF; Sengers, RCA; Mariman, E; van den Heuvel, LP; Wendel, U; Koch, G; Smeitink, JAM
      Infantile presentation of the mtDNA A3243G tRNA(Leu(UUR)) mutation

      NEUROPEDIATRICS
    6. Jira, PE; Wanders, RJA; Smeitink, JAM; De Jong, J; Wevers, RA; Oostheim, W; Tuerlings, JHAM; Hennekam, RCM; Sengers, RCA; Waterham, HR
      Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith-Lemli-Opitz syndrome

      ANNALS OF HUMAN GENETICS
    7. Rubio-Gozalbo, ME; Dijkman, KP; van den Heuvel, LP; Sengers, RCA; Wendel, U; Smeitink, JAM
      Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutations

      HUMAN MUTATION
    8. Loeffen, JLCM; Smeitink, JAM; Trijbels, JMF; Janssen, AJM; Triepels, RH; Sengers, RCA; van den Heuvel, LP
      Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects

      HUMAN MUTATION
    9. den Broeder, E; Lippens, RJJ; van't Hof, MA; Tolboom, JJM; Sengers, RCA; van Staveren, WA
      Association between the change in nutritional status in response to tube feeding and the occurrence of infections in children with a solid tumor

      PEDIATRIC HEMATOLOGY AND ONCOLOGY
    10. Smeitink, JAM; Sengers, RCA; Trijbels, FJM; van den Heuvel, LP
      Nuclear genes and oxidative phosphorylation disorders: a review

      EUROPEAN JOURNAL OF PEDIATRICS
    11. Rubio-Gozalbo, ME; Sengers, RCA; Trijbels, JMF; Doesburg, WH; Janssen, AJM; Verbeek, ALM; Smeitink, JAM
      A prognostic index as diagnostic strategy in children suspected of mitochondriocytopathy

      NEUROPEDIATRICS
    12. 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
      Nasogastric tube feeding in children with cancer: The effect of two different formulas on weight, body composition, and serum protein concentrations

      JOURNAL OF PARENTERAL AND ENTERAL NUTRITION
    13. Jira, PE; Wevers, RA; de Jong, J; Rubio-Gozalbo, E; Janssen-Zijlstra, FSM; van Heyst, AFJ; Sengers, RCA; Smeitink, JAM
      Simvastatin: a new therapeutic approach for Smith-Lemli-Opitz syndrome

      JOURNAL OF LIPID RESEARCH
    14. Willemsen, MAAP; Rotteveel, JJ; van Domburg, PHMF; Gabreels, FJM; Mayatepek, E; Sengers, RCA
      Preterm birth in Sjogren-Larsson syndrome

      NEUROPEDIATRICS
    15. Rubio-Gozalbo, ME; Smeitink, JAM; Ruitenbeek, W; Ter Laak, H; Mullaart, RA; Schuelke, M; Mariman, ECM; Sengers, RCA; Gabreels, FJM
      Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency

      NEUROLOGY
    16. DENBROEDER E; LIPPENS RJJ; VANTHOF MA; TOLBOOM JJM; VANSTAVEREN WA; HOFMAN Z; SENGERS RCA
      EFFECTS OF NASO-GASTRIC TUBE-FEEDING ON THE NUTRITIONAL-STATUS OF CHILDREN WITH CANCER

      European journal of clinical nutrition
    17. TERLAAK HJ; LEYTEN QH; GABREELS FJM; KUPPEN H; RENIER WO; SENGERS RCA
      LAMININ-ALPHA(2) (MEROSIN), BETA-DYSTROGLYCAN, ALPHA-SARCOGLYCAN (ADHALIN), AND DYSTROPHIN EXPRESSION IN CONGENITAL MUSCULAR-DYSTROPHIES - AN IMMUNOHISTOCHEMICAL STUDY

      Clinical neurology and neurosurgery
    18. RUBIOGOZALBO ME; RUITENBEEK W; WENDEL U; SENGERS RCA; TRIJBELS JMF; SMEITINK JAM
      SYSTEMIC INFANTILE COMPLEX-I DEFICIENCY WITH FATAL OUTCOME IN 2 BROTHERS

      Neuropediatrics
    19. SEMMEKROT BA; WESSELING P; BRUINENBERG JFM; GABREELS FM; TERLAAK H; SENGERS RCA
      INFANTILE MOTOR-NEURON DISEASE WITH AUTONOMIC DYSFUNCTION AND BUNINA BODIES

      Acta Neuropathologica
    20. WESSELING P; SENUNEKROT BA; BRUINENBERG JFM; GABREES FM; TERLAAK H; SENGERS RCA
      EARLY-INFANTILE MOTOR-NEURON DISORDER WITH BUNINA BODIES

      Brain pathology
    21. VANSPRONSEN FJ; VERKERK PH; VANHOUTEN M; SMIT GPA; VANDERMEER SB; BAKKER HD; SENGERS RCA
      DOES IMPAIRED GROWTH OF PKU PATIENTS CORRELATE WITH THE STRICTNESS OFDIETARY-TREATMENT

      Acta paediatrica
    22. WILLEMSEN MAAP; VANOORT AM; TERLAAK HJ; SENGERS RCA; GABREELS FJM
      MULTICORE MYOPATHY WITH RESTRICTIVE CARDIOMYOPATHY

      Acta paediatrica
    23. RUBIOGOZALBO ME; RUITENBEEK W; BENTLAGE HACM; SCHAGGER H; SENGERS RCA; TRIJBELS JMF; TERLAAK HJ; MARIMAN ECM; BAKKER MM; DEJAGER J; SMEITINK JAM
      FAVORABLE CLINICAL COURSE IN AN INFANT WITH SEVERE DEFICIENCY OF COMPLEX-III OF THE RESPIRATORY-CHAIN COMBINED WITH LESS SEVERE DEFICIENCIES OF COMPLEX-I, COMPLEX-II AND COMPLEX-IV

      European journal of pediatrics
    24. TRIJBELS FJM; RUITENBEEK W; HUIZING M; WENDEL U; SMEITINK JAM; SENGERS RCA
      DEFECTS IN THE MITOCHONDRIAL ENERGY-METABOLISM OUTSIDE THE RESPIRATORY-CHAIN AND THE PYRUVATE-DEHYDROGENASE COMPLEX

      Molecular and cellular biochemistry
    25. MOURMANS J; WENDEL U; BENTLAGE HACM; TRIJBELS JMF; SMEITINK JAM; DECOO IFM; GABREELS FJM; SENGERS RCA; RUITENBEEK W
      CLINICAL HETEROGENEITY IN RESPIRATORY-CHAIN COMPLEX-III DEFICIENCY INCHILDHOOD

      Journal of the neurological sciences
    26. MULLENERS WM; VANRAVENSWAAY CMA; GABREELS FJM; HAMEL BCJ; VANOORT A; SENGERS RCA
      SPINAL MUSCULAR-ATROPHY COMBINED WITH CONGENITAL HEART-DISEASE - A REPORT OF 2 CASES

      Neuropediatrics
    27. TRIJBELS JMF; RUITENBEEK W; SENGERS RCA; JANSSEN AJM; VANOOST BA
      BENIGN MITOCHONDRIAL ENCEPHALOMYOPATHY IN A PATIENT WITH COMPLEX-I DEFICIENCY

      Journal of inherited metabolic disease
    28. DEBOODE WP; SEMMEKROT BA; TERLAAK HJ; VANDERBURGT CJAM; DRAAISMA JMT; LOMMEN EJP; SENGERS RCA; VANWIJKHOEK JM
      MYOPATHOLOGY IN PATIENTS WITH A NOONAN PHENOTYPE

      Acta Neuropathologica
    29. VANDERVEN PFM; JAP PHK; BARTH PG; SENGERS RCA; RAMAEKERS FCS; STADHOUDERS AM
      ABNORMAL EXPRESSION OF INTERMEDIATE FILAMENT PROTEINS IN X-LINKED MYOTUBULAR MYOPATHY IS NOT REPRODUCED IN-VITRO

      Neuromuscular disorders
    30. WENDEL U; RUITENBEEK W; BENTLAGE HACM; SENGERS RCA; TRIJBELS JMF
      NEONATAL DETONI-DEBRE-FANCONI-SYNDROME DUE TO A DEFECT IN COMPLEX-IIIOF THE RESPIRATORY-CHAIN

      European journal of pediatrics
    31. LEYTEN QH; GABREELS FJM; RENIER WO; VANENGELEN BGM; TERLAAK HJ; SENGERS RCA; THIJSSEN HOM
      WHITE-MATTER ABNORMALITIES IN CONGENITAL MUSCULAR-DYSTROPHY

      Journal of the neurological sciences
    32. VANDERVEN PFM; JAP PHK; TERLAAK HJ; NONAKA I; BARTH PG; SENGERS RCA; STADHOUDERS AM; RAMAEKERS FCS
      IMMUNOPHENOTYPING OF CONGENITAL MYOPATHIES - DISORGANIZATION OF SARCOMERIC, CYTOSKELETAL AND EXTRACELLULAR-MATRIX PROTEINS

      Journal of the neurological sciences
    33. BENTLAGE HACM; JANSSEN AJM; CHOMYN A; ATTARDI G; WALKER JE; SCHAGGER H; SENGERS RCA; TRIJBELS FJM
      MULTIPLE DEFICIENCIES OF MITOCHONDRIAL DNA-ENCODED AND NUCLEAR-ENCODED SUBUNITS OF RESPIRATORY NADH DEHYDROGENASE DETECTED WITH PEPTIDE-SPECIFIC AND SUBUNIT-SPECIFIC ANTIBODIES IN MITOCHONDRIAL MYOPATHIES

      Biochimica et biophysica acta. Biomembranes
    34. VANDERSCHOT LW; DOESBURG WH; SENGERS RCA
      THE PHENYLALANINE RESPONSE CURVE IN RELATION TO GROWTH AND MENTAL-DEVELOPMENT IN THE FIRST YEARS OF LIFE

      Acta paediatrica
    35. VERKERK PH; VANSPRONSEN FJ; VANHOUTEN M; SMIT GPA; SENGERS RCA
      PREDICTORS OF MEAN PHENYLALANINE LEVELS DURING THE FIRST 5 YEARS OF LIFE IN PATIENTS WITH PHENYLKETONURIA WHO WERE TREATED EARLY

      Acta paediatrica
    36. DRAAISMA JMT; VANKESTEREN IC; DANIELS O; SENGERS RCA
      DILATED CARDIOMYOPATHY WITH 3-METHYLGLUTACONIC ACIDURIA

      Pediatric cardiology
    37. VERKERK PH; VANSPRONSEN FJ; SMIT GPA; SENGERS RCA
      IMPAIRED PRENATAL AND POSTNATAL-GROWTH IN DUTCH PATIENTS WITH PHENYLKETONURIA

      Archives of Disease in Childhood
    38. SPERL W; TRIJBELS JMF; RUITENBEEK W; VANLAACK HLJM; JANSSEN AJM; KERKHOF CMC; SENGERS RCA
      MEASUREMENT OF TOTALLY ACTIVATED PYRUVATE-DEHYDROGENASE COMPLEX ACTIVITY IN HUMAN MUSCLE - EVALUATION OF A USEFUL ASSAY

      Enzyme & protein
    39. ILES DE; SEGERS B; SENGERS RCA; MONSIEURS K; HEYTENS L; HALSALL PJ; HOPKINS PM; ELLIS FR; HALLCURRAN JL; STEWART AD; WIERINGA B
      GENETIC-MAPPING OF THE BETA(1)-SUBUNIT AND GAMMA-SUBUNIT OF THE HUMANSKELETAL-MUSCLE L-TYPE VOLTAGE-DEPENDENT CALCIUM-CHANNEL ON CHROMOSOME-17Q AND EXCLUSION AS CANDIDATE GENES FOR MALIGNANT HYPERTHERMIA SUSCEPTIBILITY

      Human molecular genetics
    40. ARTS WFM; LOONEN MCB; SENGERS RCA; SLOOFF JL
      X-LINKED ATAXIA, WEAKNESS, DEAFNESS, AND LOSS OF VISION IN EARLY-CHILDHOOD WITH A FATAL COURSE

      Annals of neurology
    41. LEYTEN QH; TERLAAK HJ; GABREELS FJM; RENIER WO; RENKAWEK K; SENGERS RCA
      CONGENITAL MUSCULAR-DYSTROPHY - A STUDY ON THE VARIABILITY OF MORPHOLOGICAL-CHANGES AND DYSTROPHIN DISTRIBUTION IN MUSCLE BIOPSIES

      Acta Neuropathologica


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 06/06/20 alle ore 11:11:08