Roels F - Search Results

1

Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidation.

Van Maldergem L, Espeel M, Wanders RJ, Roels F, Gerard P, Scalais E, Mannaerts GP, Casteels M, Gillerot Y. Van Maldergem L, et al. Among authors: roels f. Neuromuscul Disord. 1992;2(3):217-24. doi: 10.1016/0960-8966(92)90009-u. Neuromuscul Disord. 1992. PMID: 1483048

2

Peroxisomal localization of the immunoreactive beta-oxidation enzymes in a neonate with a beta-oxidation defect. Pathological observations in liver, adrenal cortex and kidney.

Espeel M, Roels F, Van Maldergem L, De Craemer D, Dacremont G, Wanders RJ, Hashimoto T. Espeel M, et al. Among authors: roels f. Virchows Arch A Pathol Anat Histopathol. 1991;419(4):301-8. doi: 10.1007/BF01606521. Virchows Arch A Pathol Anat Histopathol. 1991. PMID: 1949612

3

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.

4

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

5

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.

6

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

7

X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus.

Van Maldergem L, Espeel M, Roels F, Petit C, Dacremont G, Wanders RJ, Verloes A, Gillerot Y. Van Maldergem L, et al. Among authors: roels f. Hum Genet. 1991 Oct;87(6):661-4. doi: 10.1007/BF00201721. Hum Genet. 1991. PMID: 1937466

8

Immunocytochemical localization of peroxisomal beta-oxidation enzymes in human fetal liver.

Espeel M, Jauniaux E, Hashimoto T, Roels F. Espeel M, et al. Among authors: roels f. Prenat Diagn. 1990 Jun;10(6):349-57. doi: 10.1002/pd.1970100602. Prenat Diagn. 1990. PMID: 2217076

9

Immunocytochemical detection of peroxisomal beta-oxidation enzymes in cryostat and paraffin sections of human post mortem liver.

Espeel M, Hashimoto T, De Craemer D, Roels F. Espeel M, et al. Among authors: roels f. Histochem J. 1990 Jan;22(1):57-62. doi: 10.1007/BF01962880. Histochem J. 1990. PMID: 1690189

10

Liver pathology and immunocytochemistry in congenital peroxisomal diseases: a review.

Roels F, Espeel M, De Craemer D. Roels F, et al. J Inherit Metab Dis. 1991;14(6):853-75. doi: 10.1007/BF01800464. J Inherit Metab Dis. 1991. PMID: 1779645 Review.

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