Roels F - Search Results

1

Peroxisome mosaicism in the livers of peroxisomal deficiency patients.

Espeel M, Mandel H, Poggi F, Smeitink JA, Wanders RJ, Kerckaert I, Schutgens RB, Saudubray JM, Poll-The BT, Roels F. Espeel M, et al. Among authors: roels f. Hepatology. 1995 Aug;22(2):497-504. Hepatology. 1995. PMID: 7635418

2

Human liver pathology in peroxisomal diseases: a review including novel data.

Roels F, Espeel M, Poggi F, Mandel H, van Maldergem L, Saudubray JM. Roels F, et al. Biochimie. 1993;75(3-4):281-92. doi: 10.1016/0300-9084(93)90088-a. Biochimie. 1993. PMID: 7685191 Review.

3

Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disorders.

Espeel M, Roels F, Giros M, Mandel H, Peltier A, Poggi F, Poll-The BT, Smeitink JA, Van Maldergem L, Santos MJ. Espeel M, et al. Among authors: roels f. Eur J Cell Biol. 1995 Aug;67(4):319-27. Eur J Cell Biol. 1995. PMID: 8521871

4

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

Kerckaert I, Poll-The BT, Espeel M, Duran M, Roeleveld AB, Wanders RJ, Roels F. Kerckaert I, et al. Among authors: roels f. Virchows Arch. 2000 May;436(5):459-65. doi: 10.1007/s004280050473. Virchows Arch. 2000. PMID: 10881739

5

Hepatocellular peroxisomes in human alcoholic and drug-induced hepatitis: a quantitative study.

De Craemer D, Kerckaert I, Roels F. De Craemer D, et al. Among authors: roels f. Hepatology. 1991 Nov;14(5):811-7. doi: 10.1002/hep.1840140512. Hepatology. 1991. PMID: 1937386

6

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

De Craemer D, Zweens MJ, Lyonnet S, Wanders RJ, Poll-The BT, Schutgens RB, Waelkens JJ, Saudubray JM, Roels F. De Craemer D, et al. Among authors: roels f. Virchows Arch A Pathol Anat Histopathol. 1991;419(6):523-5. doi: 10.1007/BF01650683. Virchows Arch A Pathol Anat Histopathol. 1991. PMID: 1750197

7

Human peroxisomal disorders.

Depreter M, Espeel M, Roels F. Depreter M, et al. Among authors: roels f. Microsc Res Tech. 2003 Jun 1;61(2):203-23. doi: 10.1002/jemt.10330. Microsc Res Tech. 2003. PMID: 12740827 Review.

8

A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).

Poll-The BT, Roels F, Ogier H, Scotto J, Vamecq J, Schutgens RB, Wanders RJ, van Roermund CW, van Wijland MJ, Schram AW, et al. Poll-The BT, et al. Among authors: roels f. Am J Hum Genet. 1988 Mar;42(3):422-34. Am J Hum Genet. 1988. PMID: 2894756 Free PMC article.

9

Hepatic peroxisomes in adrenoleukodystrophy and related syndromes: cytochemical and morphometric data.

Roels F, Pauwels M, Poll-Thé BT, Scotto J, Ogier H, Aubourg P, Saudubray JM. Roels F, et al. Virchows Arch A Pathol Anat Histopathol. 1988;413(4):275-85. doi: 10.1007/BF00783019. Virchows Arch A Pathol Anat Histopathol. 1988. PMID: 3140473

10

A new type of peroxisomal disorder with variable expression in liver and fibroblasts.

Mandel H, Espeel M, Roels F, Sofer N, Luder A, Iancu TC, Aizin A, Berant M, Wanders RJ, Schutgens RB. Mandel H, et al. Among authors: roels f. J Pediatr. 1994 Oct;125(4):549-55. doi: 10.1016/s0022-3476(94)70006-0. J Pediatr. 1994. PMID: 7931872

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