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Results: 1-25 | 26-26
Results: 1-25/26
EFFECTS OF NASO-GASTRIC TUBE-FEEDING ON THE NUTRITIONAL-STATUS OF CHILDREN WITH CANCER
Authors: DENBROEDER E LIPPENS RJJ VANTHOF MA TOLBOOM JJM VANSTAVEREN WA HOFMAN Z SENGERS RCA
Citation: E. Denbroeder et al., EFFECTS OF NASO-GASTRIC TUBE-FEEDING ON THE NUTRITIONAL-STATUS OF CHILDREN WITH CANCER, European journal of clinical nutrition, 52(7), 1998, pp. 494-500
LAMININ-ALPHA(2) (MEROSIN), BETA-DYSTROGLYCAN, ALPHA-SARCOGLYCAN (ADHALIN), AND DYSTROPHIN EXPRESSION IN CONGENITAL MUSCULAR-DYSTROPHIES - AN IMMUNOHISTOCHEMICAL STUDY
Authors: TERLAAK HJ LEYTEN QH GABREELS FJM KUPPEN H RENIER WO SENGERS RCA
Citation: Hj. Terlaak et al., LAMININ-ALPHA(2) (MEROSIN), BETA-DYSTROGLYCAN, ALPHA-SARCOGLYCAN (ADHALIN), AND DYSTROPHIN EXPRESSION IN CONGENITAL MUSCULAR-DYSTROPHIES - AN IMMUNOHISTOCHEMICAL STUDY, Clinical neurology and neurosurgery, 100(1), 1998, pp. 5-10
SYSTEMIC INFANTILE COMPLEX-I DEFICIENCY WITH FATAL OUTCOME IN 2 BROTHERS
Authors: RUBIOGOZALBO ME RUITENBEEK W WENDEL U SENGERS RCA TRIJBELS JMF SMEITINK JAM
Citation: Me. Rubiogozalbo et al., SYSTEMIC INFANTILE COMPLEX-I DEFICIENCY WITH FATAL OUTCOME IN 2 BROTHERS, Neuropediatrics, 29(1), 1998, pp. 43-45
INFANTILE MOTOR-NEURON DISEASE WITH AUTONOMIC DYSFUNCTION AND BUNINA BODIES
Authors: SEMMEKROT BA WESSELING P BRUINENBERG JFM GABREELS FM TERLAAK H SENGERS RCA
Citation: Ba. Semmekrot et al., INFANTILE MOTOR-NEURON DISEASE WITH AUTONOMIC DYSFUNCTION AND BUNINA BODIES, Acta Neuropathologica, 95(1), 1998, pp. 104-106
EARLY-INFANTILE MOTOR-NEURON DISORDER WITH BUNINA BODIES
Authors: WESSELING P SENUNEKROT BA BRUINENBERG JFM GABREES FM TERLAAK H SENGERS RCA
Citation: P. Wesseling et al., EARLY-INFANTILE MOTOR-NEURON DISORDER WITH BUNINA BODIES, Brain pathology, 7(4), 1997, pp. 1074-1074
DOES IMPAIRED GROWTH OF PKU PATIENTS CORRELATE WITH THE STRICTNESS OFDIETARY-TREATMENT
Authors: VANSPRONSEN FJ VERKERK PH VANHOUTEN M SMIT GPA VANDERMEER SB BAKKER HD SENGERS RCA
Citation: Fj. Vanspronsen et al., DOES IMPAIRED GROWTH OF PKU PATIENTS CORRELATE WITH THE STRICTNESS OFDIETARY-TREATMENT, Acta paediatrica, 86(8), 1997, pp. 816-818
MULTICORE MYOPATHY WITH RESTRICTIVE CARDIOMYOPATHY
Authors: WILLEMSEN MAAP VANOORT AM TERLAAK HJ SENGERS RCA GABREELS FJM
Citation: Maap. Willemsen et al., MULTICORE MYOPATHY WITH RESTRICTIVE CARDIOMYOPATHY, Acta paediatrica, 86(11), 1997, pp. 1271-1274
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
Authors: RUBIOGOZALBO ME RUITENBEEK W BENTLAGE HACM SCHAGGER H SENGERS RCA TRIJBELS JMF TERLAAK HJ MARIMAN ECM BAKKER MM DEJAGER J SMEITINK JAM
Citation: Me. Rubiogozalbo et al., 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, 156(12), 1997, pp. 931-934
DEFECTS IN THE MITOCHONDRIAL ENERGY-METABOLISM OUTSIDE THE RESPIRATORY-CHAIN AND THE PYRUVATE-DEHYDROGENASE COMPLEX
Authors: TRIJBELS FJM RUITENBEEK W HUIZING M WENDEL U SMEITINK JAM SENGERS RCA
Citation: Fjm. Trijbels et al., DEFECTS IN THE MITOCHONDRIAL ENERGY-METABOLISM OUTSIDE THE RESPIRATORY-CHAIN AND THE PYRUVATE-DEHYDROGENASE COMPLEX, Molecular and cellular biochemistry, 174(1-2), 1997, pp. 243-247
CLINICAL HETEROGENEITY IN RESPIRATORY-CHAIN COMPLEX-III DEFICIENCY INCHILDHOOD
Authors: MOURMANS J WENDEL U BENTLAGE HACM TRIJBELS JMF SMEITINK JAM DECOO IFM GABREELS FJM SENGERS RCA RUITENBEEK W
Citation: J. Mourmans et al., CLINICAL HETEROGENEITY IN RESPIRATORY-CHAIN COMPLEX-III DEFICIENCY INCHILDHOOD, Journal of the neurological sciences, 149(1), 1997, pp. 111-117
SPINAL MUSCULAR-ATROPHY COMBINED WITH CONGENITAL HEART-DISEASE - A REPORT OF 2 CASES
Authors: MULLENERS WM VANRAVENSWAAY CMA GABREELS FJM HAMEL BCJ VANOORT A SENGERS RCA
Citation: Wm. Mulleners et al., SPINAL MUSCULAR-ATROPHY COMBINED WITH CONGENITAL HEART-DISEASE - A REPORT OF 2 CASES, Neuropediatrics, 27(6), 1996, pp. 333-334
BENIGN MITOCHONDRIAL ENCEPHALOMYOPATHY IN A PATIENT WITH COMPLEX-I DEFICIENCY
Authors: TRIJBELS JMF RUITENBEEK W SENGERS RCA JANSSEN AJM VANOOST BA
Citation: Jmf. Trijbels et al., BENIGN MITOCHONDRIAL ENCEPHALOMYOPATHY IN A PATIENT WITH COMPLEX-I DEFICIENCY, Journal of inherited metabolic disease, 19(2), 1996, pp. 149-152
MYOPATHOLOGY IN PATIENTS WITH A NOONAN PHENOTYPE
Authors: DEBOODE WP SEMMEKROT BA TERLAAK HJ VANDERBURGT CJAM DRAAISMA JMT LOMMEN EJP SENGERS RCA VANWIJKHOEK JM
Citation: Wp. Deboode et al., MYOPATHOLOGY IN PATIENTS WITH A NOONAN PHENOTYPE, Acta Neuropathologica, 92(6), 1996, pp. 597-602
ABNORMAL EXPRESSION OF INTERMEDIATE FILAMENT PROTEINS IN X-LINKED MYOTUBULAR MYOPATHY IS NOT REPRODUCED IN-VITRO
Authors: VANDERVEN PFM JAP PHK BARTH PG SENGERS RCA RAMAEKERS FCS STADHOUDERS AM
Citation: Pfm. Vanderven et al., ABNORMAL EXPRESSION OF INTERMEDIATE FILAMENT PROTEINS IN X-LINKED MYOTUBULAR MYOPATHY IS NOT REPRODUCED IN-VITRO, Neuromuscular disorders, 5(4), 1995, pp. 267-275
NEONATAL DETONI-DEBRE-FANCONI-SYNDROME DUE TO A DEFECT IN COMPLEX-IIIOF THE RESPIRATORY-CHAIN
Authors: WENDEL U RUITENBEEK W BENTLAGE HACM SENGERS RCA TRIJBELS JMF
Citation: U. Wendel et al., NEONATAL DETONI-DEBRE-FANCONI-SYNDROME DUE TO A DEFECT IN COMPLEX-IIIOF THE RESPIRATORY-CHAIN, European journal of pediatrics, 154(11), 1995, pp. 915-918
WHITE-MATTER ABNORMALITIES IN CONGENITAL MUSCULAR-DYSTROPHY
Authors: LEYTEN QH GABREELS FJM RENIER WO VANENGELEN BGM TERLAAK HJ SENGERS RCA THIJSSEN HOM
Citation: Qh. Leyten et al., WHITE-MATTER ABNORMALITIES IN CONGENITAL MUSCULAR-DYSTROPHY, Journal of the neurological sciences, 129(2), 1995, pp. 162-169
IMMUNOPHENOTYPING OF CONGENITAL MYOPATHIES - DISORGANIZATION OF SARCOMERIC, CYTOSKELETAL AND EXTRACELLULAR-MATRIX PROTEINS
Authors: VANDERVEN PFM JAP PHK TERLAAK HJ NONAKA I BARTH PG SENGERS RCA STADHOUDERS AM RAMAEKERS FCS
Citation: Pfm. Vanderven et al., IMMUNOPHENOTYPING OF CONGENITAL MYOPATHIES - DISORGANIZATION OF SARCOMERIC, CYTOSKELETAL AND EXTRACELLULAR-MATRIX PROTEINS, Journal of the neurological sciences, 129(2), 1995, pp. 199-213
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
Authors: BENTLAGE HACM JANSSEN AJM CHOMYN A ATTARDI G WALKER JE SCHAGGER H SENGERS RCA TRIJBELS FJM
Citation: Hacm. Bentlage et al., 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, 1234(1), 1995, pp. 63-73
THE PHENYLALANINE RESPONSE CURVE IN RELATION TO GROWTH AND MENTAL-DEVELOPMENT IN THE FIRST YEARS OF LIFE
Authors: VANDERSCHOT LW DOESBURG WH SENGERS RCA
Citation: Lw. Vanderschot et al., THE PHENYLALANINE RESPONSE CURVE IN RELATION TO GROWTH AND MENTAL-DEVELOPMENT IN THE FIRST YEARS OF LIFE, Acta paediatrica, 83, 1994, pp. 68-69
PREDICTORS OF MEAN PHENYLALANINE LEVELS DURING THE FIRST 5 YEARS OF LIFE IN PATIENTS WITH PHENYLKETONURIA WHO WERE TREATED EARLY
Authors: VERKERK PH VANSPRONSEN FJ VANHOUTEN M SMIT GPA SENGERS RCA
Citation: Ph. Verkerk et al., PREDICTORS OF MEAN PHENYLALANINE LEVELS DURING THE FIRST 5 YEARS OF LIFE IN PATIENTS WITH PHENYLKETONURIA WHO WERE TREATED EARLY, Acta paediatrica, 83, 1994, pp. 70-72
DILATED CARDIOMYOPATHY WITH 3-METHYLGLUTACONIC ACIDURIA
Authors: DRAAISMA JMT VANKESTEREN IC DANIELS O SENGERS RCA
Citation: Jmt. Draaisma et al., DILATED CARDIOMYOPATHY WITH 3-METHYLGLUTACONIC ACIDURIA, Pediatric cardiology, 15(2), 1994, pp. 89-90
IMPAIRED PRENATAL AND POSTNATAL-GROWTH IN DUTCH PATIENTS WITH PHENYLKETONURIA
Authors: VERKERK PH VANSPRONSEN FJ SMIT GPA SENGERS RCA
Citation: Ph. Verkerk et al., IMPAIRED PRENATAL AND POSTNATAL-GROWTH IN DUTCH PATIENTS WITH PHENYLKETONURIA, Archives of Disease in Childhood, 71(2), 1994, pp. 114-118
MEASUREMENT OF TOTALLY ACTIVATED PYRUVATE-DEHYDROGENASE COMPLEX ACTIVITY IN HUMAN MUSCLE - EVALUATION OF A USEFUL ASSAY
Authors: SPERL W TRIJBELS JMF RUITENBEEK W VANLAACK HLJM JANSSEN AJM KERKHOF CMC SENGERS RCA
Citation: W. Sperl et al., MEASUREMENT OF TOTALLY ACTIVATED PYRUVATE-DEHYDROGENASE COMPLEX ACTIVITY IN HUMAN MUSCLE - EVALUATION OF A USEFUL ASSAY, Enzyme & protein, 47(1), 1993, pp. 37-46
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
Authors: ILES DE SEGERS B SENGERS RCA MONSIEURS K HEYTENS L HALSALL PJ HOPKINS PM ELLIS FR HALLCURRAN JL STEWART AD WIERINGA B
Citation: De. Iles et al., 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, 2(7), 1993, pp. 863-868
X-LINKED ATAXIA, WEAKNESS, DEAFNESS, AND LOSS OF VISION IN EARLY-CHILDHOOD WITH A FATAL COURSE
Authors: ARTS WFM LOONEN MCB SENGERS RCA SLOOFF JL
Citation: Wfm. Arts et al., X-LINKED ATAXIA, WEAKNESS, DEAFNESS, AND LOSS OF VISION IN EARLY-CHILDHOOD WITH A FATAL COURSE, Annals of neurology, 33(5), 1993, pp. 535-539
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