AAAAAA
Results:
1-15
|
Results: 15
Authors:
DEJONG JGN
AERTS JMFG
VANWEELY S
HOLLAK CEM
VANPELT J
VANWOERKOM LMJ
LIEBRANDVANSAMBEEK MLF
WEVERS RA
Citation: Jgn. Dejong et al., OLIGOSACCHARIDE EXCRETION IN ADULT GAUCHER-DISEASE, Journal of inherited metabolic disease, 21(1), 1998, pp. 49-59
Authors:
VANASSELT DZB
KARLIETIS MHJ
POELS PJE
DEJONG JGN
WEVERS RA
HOEFNAGELS WHL
Citation: Dzb. Vanasselt et al., CEREBROSPINAL-FLUID METHYLMALONIC ACID CONCENTRATIONS IN NEUROLOGICALPATIENTS WITH LOW AND NORMAL SERUM COBALAMIN CONCENTRATIONS, Acta neurologica Scandinavica, 97(6), 1998, pp. 413-416
Authors:
WEVERS RA
ENGELKE U
ROTTEVEEL JJ
HEERSCHAP A
DEJONG JGN
ABELING NGGM
VANGENNIP AH
DEABREU RA
Citation: Ra. Wevers et al., H-1-NMR SPECTROSCOPY OF BODY-FLUIDS IN PATIENTS WITH INBORN-ERRORS OFPURINE AND PYRIMIDINE METABOLISM, Journal of inherited metabolic disease, 20(3), 1997, pp. 345-350
Authors:
JIRA PE
DEJONG JGN
JANSSENZIJLSTRA FSM
WENDEL U
WEVERS RA
Citation: Pe. Jira et al., PITFALLS IN MEASURING PLASMA-CHOLESTEROL IN THE SMITH-LEMLI-OPITZ SYNDROME, Clinical chemistry, 43(1), 1997, pp. 129-133
Authors:
LAMERS KJB
DEJONG JGN
Citation: Kjb. Lamers et Jgn. Dejong, CEREBROSPINAL-FLUID FREE KAPPA-LIGHT-CHAINS IN MS DIAGNOSTICS - COMPARISON WITH IGG TESTS, Journal of neurochemistry, 66, 1996, pp. 26-26
Authors:
KEULEMANS JLM
REUSER AJJ
KROOS MA
WILLEMSEN R
HERMANS MMP
VANDENOUWELAND AMW
DEJONG JGN
WEVERS RA
RENIER WO
SCHINDLER D
COLL MJ
CHABAS A
SAKURABA H
SUZUKI Y
VANDIGGELEN OP
Citation: Jlm. Keulemans et al., HUMAN ALPHA-N-ACETYLGALACTOSAMINIDASE (ALPHA-NAGA) DEFICIENCY - NEW MUTATIONS AND THE PARADOX BETWEEN GENOTYPE AND PHENOTYPE, Journal of Medical Genetics, 33(6), 1996, pp. 458-464
Authors:
KEUZENKAMPJANSEN CW
VANBAAL JM
DEABREU R
DEJONG JGN
ZUIDERENT R
TRIJBELS JMF
Citation: Cw. Keuzenkampjansen et al., DETECTION AND IDENTIFICATION OF 6-METHYLMERCAPTO-8-HYDROXYPURINE, A MAJOR METABOLITE OF 6-MERCAPTOPURINE, IN PLASMA DURING INTRAVENOUS ADMINISTRATION, Clinical chemistry, 42(3), 1996, pp. 380-386
Authors:
LUYTEN JAFM
WENINK PW
STEENBERGENSPANJERS GCH
WEVERS RA
VANAMSTEL HKP
DEJONG JGN
VANDENHEUVEL LPWJ
Citation: Jafm. Luyten et al., METACHROMATIC LEUKODYSTROPHY - A 12-BP DELETION IN EXON-2 OF THE ARYLSULFATASE-A GENE IN A LATE INFANTILE VARIANT, Human genetics, 96(3), 1995, pp. 357-360
Authors:
LAMERS KJB
DEJONG JGN
JONGEN PJH
KOCKJANSEN MJH
TEUNESEN MA
PRUDONROSMULDER EMW
Citation: Kjb. Lamers et al., CEREBROSPINAL-FLUID FREE KAPPA-LIGHT-CHAINS VERSUS IGG FINDINGS IN NEUROLOGICAL DISORDERS - QUALITATIVE AND QUANTITATIVE MEASUREMENTS, Journal of neuroimmunology, 62(1), 1995, pp. 19-25
Authors:
WEVERS RA
ENGELKE U
WENDEL U
DEJONG JGN
GABREELS FJM
HEERSCHAP A
Citation: Ra. Wevers et al., STANDARDIZED METHOD FOR HIGH-RESOLUTION H-1-NMR OF CEREBROSPINAL-FLUID, Clinical chemistry, 41(5), 1995, pp. 744-751
Authors:
LEENDERS RGG
DEJONG JGN
WEVERS RA
Citation: Rgg. Leenders et al., EXTRACTION AND PURIFICATION OF GANGLIOSIDES FROM PLASMA AND FIBROBLASTS BEFORE ANALYSIS BY THIN-LAYER CHROMATOGRAPHY, Annals of clinical biochemistry, 32, 1995, pp. 68-73
Authors:
HAGEMAN ATM
GABREELS FJM
DEJONG JGN
GABREELSFESTEN AAWM
VANDENBERG CJMG
VANOOST BA
WEVERS RA
Citation: Atm. Hageman et al., CLINICAL SYMPTOMS OF ADULT METACHROMATIC LEUKODYSTROPHY AND ARYLSULFATASE-A PSEUDODEFICIENCY, Archives of neurology, 52(4), 1995, pp. 408-413
Authors:
VANAMSTEL JKP
JANSEN RPM
DEJONG JGN
HAMEL BCJ
WEVERS RA
Citation: Jkp. Vanamstel et al., 6 NOVEL MUTATIONS IN THE ALPHA-GALACTOSIDASE-A GENE IN FAMILIES WITH FABRY DISEASE, Human molecular genetics, 3(3), 1994, pp. 503-505
Authors:
PEELEN GOH
DEJONG JGN
WEVERS RA
Citation: Goh. Peelen et al., HPLC ANALYSIS OF OLIGOSACCHARIDES IN URINE FROM OLIGOSACCHARIDOSIS PATIENTS, Clinical chemistry, 40(6), 1994, pp. 914-921
Authors:
DEJONG JGN
HEIJS WMJ
WEVERS RA
Citation: Jgn. Dejong et al., MUCOPOLYSACCHARIDOSES SCREENING - DIMETHYLMETHYLENE BLUE VERSUS ALCIAN BLUE, Annals of clinical biochemistry, 31, 1994, pp. 267-271
Risultati:
1-15
|