Roels F - Search Results

1

Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.

Poll-The BT, Saudubray JM, Ogier HA, Odièvre M, Scotto JM, Monnens L, Govaerts LC, Roels F, Cornelis A, Schutgens RB, et al. Poll-The BT, et al. Among authors: roels f. Eur J Pediatr. 1987 Sep;146(5):477-83. doi: 10.1007/BF00441598. Eur J Pediatr. 1987. PMID: 2445576

2

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.

3

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

4

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

5

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

Baumgartner MR, Poll-The BT, Verhoeven NM, Jakobs C, Espeel M, Roels F, Rabier D, Levade T, Rolland MO, Martinez M, Wanders RJ, Saudubray JM. Baumgartner MR, et al. Among authors: roels f. Ann Neurol. 1998 Nov;44(5):720-30. doi: 10.1002/ana.410440505. Ann Neurol. 1998. PMID: 9818927

6

Atypical refsum disease with pipecolic acidemia and abnormal catalase distribution.

Baumgartner MR, Jansen GA, Verhoeven NM, Mooyer PA, Jakobs C, Roels F, Espeel M, Fourmaintraux A, Bellet H, Wanders RJ, Saudubray JM. Baumgartner MR, et al. Among authors: roels f. Ann Neurol. 2000 Jan;47(1):109-13. Ann Neurol. 2000. PMID: 10632109

7

Absence of hepatic peroxisomes in a case of infantile Refsum's disease.

Ogier H, Roels F, Cornelis A, Poll The BT, Scotto JM, Odievre M, Sandubray JM. Ogier H, et al. Among authors: roels f. Scand J Clin Lab Invest. 1985 Dec;45(8):767-8. doi: 10.3109/00365518509155292. Scand J Clin Lab Invest. 1985. PMID: 2417305 No abstract available.

8

Hepatic peroxisomes are deficient in infantile refsum disease: a cytochemical study of 4 cases.

Roels F, Cornelis A, Poll-The BT, Aubourg P, Ogier H, Scotto J, Saudubray JM. Roels F, et al. Am J Med Genet. 1986 Oct;25(2):257-71. doi: 10.1002/ajmg.1320250210. Am J Med Genet. 1986. PMID: 2430454

9

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

10

Isolated dihydroxyacetonephosphate-acyl-transferase deficiency in rhizomelic chondrodysplasia punctata: clinical presentation, metabolic and histological findings.

Hebestreit H, Wanders RJ, Schutgens RB, Espeel M, Kerckaert I, Roels F, Schmausser B, Schrod L, Marx A. Hebestreit H, et al. Among authors: roels f. Eur J Pediatr. 1996 Dec;155(12):1035-9. doi: 10.1007/BF02532526. Eur J Pediatr. 1996. PMID: 8956940

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

162 results

Search Page

Filters