Access the full text.
Sign up today, get DeepDyve free for 14 days.
Loading next page...
/lp/wiley/alterations-of-hepatic-peroxisomes-in-tyrosinaemia-type-i-return-to-8iHJGCh685
References (13)
-
D. Craemer (2004)
Secondary alterations of human hepatocellular peroxisomesJournal of Inherited Metabolic Disease, 18
-
F. Roels (1994)
Peroxisomes: A Personal Account -
M. Espeel, M. Depreter, R. Nardacci, K. D’Herde, I. Kerckaert, S. Stefanini, F. Roels (1997)
Biogenesis of peroxisomes in fetal liverMicroscopy Research and Technique, 39
-
M. Espeel, N. Brière, D. Craemer, Eric Jauniaux, F. Roels (1993)
Catalase-negative peroxisomes in human embryonic liverCell and Tissue Research, 272
-
Ingrid Kerckaert, D. Craemer, G. Limbergen (1995)
Practical guide for morphometry of human peroxisomes on electron micrographsJournal of Inherited Metabolic Disease, 18
-
F. Roels, B. Prest, G. Pestel (1995)
Liver and chorion cytochemistryJournal of Inherited Metabolic Disease, 18
-
(1995)
Practical guide for morphometry -
Diagnosis of Human Peroxisomal Diseases -
(1997)
Hereditary tyrosin - aemia type I : an ultrastructural study of 7 patients treated with NTBC -
(1990)
Peroxisomes : experimental and human studies. Thesis -
MJ Phillips, S Poucell, J Patterson, P Valencia (1987)
The Liver: An Atlas and T ext of Ultrastructural Pathology -
(1990)
Peroxisomes : experimental and human studies -
M. Schilsky, P. Mistry (2001)
Metabolic liver diseaseCurrent Opinion in Gastroenterology, 17
- Publisher
- Wiley
- Copyright
- © SSIEM
- ISSN
- 0141-8955
- eISSN
- 1573-2665
- DOI
- 10.1023/A:1005351129336
- Publisher site
- See Article on Publisher Site
Abstract
Journal
Journal of Inherited Metabolic Disease – Wiley
Published: Jun 1, 1998