Ghent University Academic Bibliography

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Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiency.

Ingrid Kerckaert (UGent) , BT POLL-THE, Marc Espeel (UGent) , M DURAN, A ROELEVELD, R WANDERS and Frank Roels (UGent)

(2000) VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY. 436(5). p.459-465
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- Journal Article
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Alterations of hepatic peroxisomes in tyrosinaemia type I: Return to fetal type?

Ingrid Kerckaert (UGent) , TJ DE KONING, BT POLL-THE and Frank Roels (UGent)

(1998) JOURNAL OF INHERITED METABOLIC DISEASE. 21(3). p.186-190
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- Journal Article
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Clinical approach to inherited peroxisomal disorders: A series of 27 patients.

MR BAUMGARTNER, BT POLL-THE, NM VERHOEVEN, C JAKOBS, Marc Espeel (UGent) , Frank Roels (UGent) , D RABIER, T LEVADE, MO ROLLAND, M MARTINEZ, et al.

(1998) ANNALS OF NEUROLOGY. 44(5). p.720-730
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Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata

Marc Espeel (UGent) , JC Heikoop, JAM Smeitink, FA Beemer, Dirk De Craemer (UGent) , M Van Den Berg, T Hashimoto, RJA Wanders, RBH Schutgens, BT Poll-The, et al.

(1993) ULTRASTRUCTURAL PATHOLOGY. 17(6). p.623-636
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Peroxisomes are enlarged in two patients with peroxisomal diseases: novel cases

Dirk De Craemer (UGent) , MJ Zweens, S Lyonnet, RJA Wanders, BT Poll-The, JJJ Waelkens, RBH Schutgens, JM Saudubray and Frank Roels (UGent)

(1991) MICRON AND MICROSCOPICA ACTA. 22(3). p.263-264
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- Journal Article
- A1
Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency) : novel data

Dirk De Craemer (UGent) , MJ Zweens, S Lyonnet, RJA Wanders, BT Poll-The, RBH Schutgens, JJJ Waelkens, JM Saudubray and Frank Roels (UGent)

(1991) VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY. 419(6). p.523-525

Academic Bibliography

Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiency.

Alterations of hepatic peroxisomes in tyrosinaemia type I: Return to fetal type?

Clinical approach to inherited peroxisomal disorders: A series of 27 patients.

Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata

Peroxisomes are enlarged in two patients with peroxisomal diseases: novel cases

Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency) : novel data

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