Kallmann syndrome in a patient with congenital spherocytosis and an interstitial 8p11.2 deletionVERMEULEN, Stefan; MESSIAEN, Ludwine; SCHEIR, Petra et al.American journal of medical genetics. 2002, Vol 108, Num 4, pp 315-318, issn 0148-7299Article

Association between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis CVAN VLIERBERGHE, Hans; DELANGHE, Joris R; DE BIE, Sylvia et al.European journal of gastroenterology & hepatology. 2001, Vol 13, Num 9, pp 1077-1081, issn 0954-691XArticle

Measurement of peroxisomal fatty acid β-oxidation in cultured human skin fibroblastsWANDERS, R. J. A; DENIS, S; RUITER, J. P. N et al.Journal of inherited metabolic disease. 1995, Vol 18, pp 113-124, issn 0141-8955, SUP1Article

Secondary alterations of human hepatocellular peroxisomesDE CRAEMER, D.Journal of inherited metabolic disease. 1995, Vol 18, pp 181-213, issn 0141-8955, SUP1Article

Diagnosis of human peroxisomal disorders. A handbookROELS, Franck; DE BIE, Sylvia; SCHUTGENS, Ruud B. H et al.Journal of inherited metabolic disease. 1995, Vol 18, issn 0141-8955, 231 p., SUP1Serial Issue

DNA diagnosis of X-linked adrenoleukodystrophySENECA, S; LISSENS, W.Journal of inherited metabolic disease. 1995, Vol 18, pp 34-44, issn 0141-8955, SUP1Article

Measurement of very long-chain fatty acids, phytanic and pristanic acid in plasma and cultured fibroblasts by gas chromatographyDACREMONT, G; COCQUYT, G; VINCENT, G et al.Journal of inherited metabolic disease. 1995, Vol 18, pp 76-83, issn 0141-8955, SUP1Article

Liver and chorion cytochemistryROELS, F; DE PREST, B; DE PESTEL, G et al.Journal of inherited metabolic disease. 1995, Vol 18, pp 155-171, issn 0141-8955, SUP1Article

Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome. EditorialLOEYS, Bart; NUYTINCK, Lieve; DELVAUX, Isabelle et al.Archives of internal medicine (1960). 2001, Vol 161, Num 20, pp 2406-2408, issn 0003-9926, 11 p.Article

Neuropathology of peroxisomal diseasesMARTIN, J.-J.Journal of inherited metabolic disease. 1995, Vol 18, pp 19-33, issn 0141-8955, SUP1Article

Assay of plasmalogens and polyunsaturated fatty acids (PUFA) in erythrocytes and fibroblastsDACREMONT, G; VINCENT, G.Journal of inherited metabolic disease. 1995, Vol 18, pp 84-89, issn 0141-8955, SUP1Article

Activity mesurements of acyl-CoA oxidases in human liverVAN VELDHOVEN, P. P.Journal of inherited metabolic disease. 1995, Vol 18, pp 125-134, issn 0141-8955, SUP1Article

Immunocytochemical localization of peroxisomal proteins in human liver and kidneyESPEEL, M; VAN LIMBERGEN, G.Journal of inherited metabolic disease. 1995, Vol 18, pp 135-154, issn 0141-8955, SUP1Article

Diagnostic work-up of a peroxisomal patientLEROY, J. G; ESPEEL, M; GADISSEUX, J. F et al.Journal of inherited metabolic disease. 1995, Vol 18, pp 214-222, issn 0141-8955, SUP1Article

Measurement of dihydroxyacetone-phosphate acyltransferase (DHAPAT) in chorionic villous samples, blood cells and cultured cellsWANDERS, R. J. A; OFMAN, R; ROMEIJN, G. J et al.Journal of inherited metabolic disease. 1995, Vol 18, pp 90-100, issn 0141-8955, SUP1Article

Practical guide for morphometry of human peroxisomes on electron micrographsKERCKAERT, I; DE CRAEMER, D; VAN LIMBERGEN, G et al.Journal of inherited metabolic disease. 1995, Vol 18, pp 172-180, issn 0141-8955, SUP1Article