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European Journal of Cell Biology|August 1, 1995
Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disordersM Espeel, F Roels, M Giros, et al.
Hepatology (Baltimore, Md.)|August 1, 1995
Peroxisome mosaicism in the livers of peroxisomal deficiency patientsM Espeel, H Mandel, F Poggi, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1991
Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency): novel dataD De Craemer, M J Zweens, S Lyonnet, et al.
European Journal of Pediatrics|September 1, 1987
Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophyB T Poll-The, J M Saudubray, H A Ogier, et al.
Annals of Neurology|January 13, 2000
Atypical refsum disease with pipecolic acidemia and abnormal catalase distributionM R Baumgartner, G A Jansen, N M Verhoeven, et al.
Journal of Child Neurology|November 26, 1999
Diagnosis and follow-up of a case of peroxisomal disorder with peroxisomal mosaicismM Pineda, M Girós, F Roels, et al.
American Journal of Human Genetics|March 1, 1988
A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy)B T Poll-The, F Roels, H Ogier, et al.
Cell Death & Disease|April 13, 2013
Hox-C9 activates the intrinsic pathway of apoptosis and is associated with spontaneous regression in neuroblastomaH Kocak, S Ackermann, B Hero, et al.
Annals of Neurology|November 18, 1998
Clinical approach to inherited peroxisomal disorders: a series of 27 patientsM R Baumgartner, B T Poll-The, N M Verhoeven, et al.
Leukemia|January 23, 2009
The hematopoietic stem cell in chronic phase CML is characterized by a transcriptional profile resembling normal myeloid progenitor cells and reflecting loss of quiescenceI Bruns, A Czibere, J C Fischer, et al.
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