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Clinical Biochemistry|June 1, 1997
Elevated sulfatide excretion in compound heterozygotes of metachromatic leukodystrophy and ASA-pseudodeficiency alleleA Lugowska, A Tylki-Szymańska, J Berger, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|January 15, 1979
Di-, mono- and nonphytanyl triglycerides in the serum: a sensitive parameter of the phytanic acid accumulation in Refsum's diseaseB Molzer, H Bernheimer, G S Barolin, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|November 10, 1982
Detection of adrenoleukodystrophy by increased C26:0 fatty acid levels in leukocytesB Molzer, H Bernheimer, R Heller, et al.Wiener Klinische Wochenschrift|January 1, 1993
[Zellweger syndrome, neonatal adrenoleukodystrophy or infantile Refsum's disease in a case with generalized peroxisome defect?]K Schmitt, B Molzer, S Stöckler, et al.Human Genetics|September 1, 1996
A new polymorphism of arylsulfatase A within the coding regionJ Berger, M Gmach, I Faé, et al.Archiv Fur Psychiatrie Und Nervenkrankheiten|December 28, 1977
[Adult metachromatic leukodystrophy manifested as schizophrenic psychosis (author's transl)]P Kothbauer, K Jellinger, H Gross, et al.Acta Neuropathologica|January 1, 1993
Unusual orthochromatic leukodystrophy with epitheloid cells (Norman-Gullotta): increase of very long chain fatty acids in brain discloses a peroxisomal disorderB Molzer, F Gullotta, K Harzer, et al.Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|May 1, 1989
Phytanic acid and very long chain fatty acids in genetic peroxisomal disordersB Molzer, M Kainz-Korschinsky, R Sundt-Heller, et al.Journal of the Neurological Sciences|August 1, 1981
Accumulation of very long chain fatty acids is common to 3 variants of adrenoleukodystrophy (ALD). "Classical" ALD, atypical ALD (female patient) and adrenomyeloneuropathyB Molzer, H Bernheimer, H Budka, et al.Pageof 4