Espeel M - Search Results

1

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: espeel m. Ann Neurol. 1998 Nov;44(5):720-30. doi: 10.1002/ana.410440505. Ann Neurol. 1998. PMID: 9818927

2

Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease.

Baumgartner MR, Verhoeven NM, Jakobs C, Roels F, Espeel M, Martinez M, Rabier D, Wanders RJ, Saudubray JM. Baumgartner MR, et al. Among authors: espeel m. Neurology. 1998 Nov;51(5):1427-32. doi: 10.1212/wnl.51.5.1427. Neurology. 1998. PMID: 9818873

3

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: espeel m. Ann Neurol. 2000 Jan;47(1):109-13. Ann Neurol. 2000. PMID: 10632109

4

Human peroxisomal disorders.

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

5

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. Hepatology. 1995 Aug;22(2):497-504. Hepatology. 1995. PMID: 7635418

6

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: espeel m. J Pediatr. 1994 Oct;125(4):549-55. doi: 10.1016/s0022-3476(94)70006-0. J Pediatr. 1994. PMID: 7931872

7

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. Eur J Cell Biol. 1995 Aug;67(4):319-27. Eur J Cell Biol. 1995. PMID: 8521871

8

Diagnostic work-up of a peroxisomal patient.

Leroy JG, Espeel M, Gadisseux JF, Mandel H, Martinez M, Poll-The BT, Wanders RJ, Roels F. Leroy JG, et al. Among authors: espeel m. J Inherit Metab Dis. 1995;18 Suppl 1:214-22. doi: 10.1007/BF00711440. J Inherit Metab Dis. 1995. PMID: 9053553 Review. No abstract available.

9

Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluria.

Van Acker KJ, Eyskens FJ, Espeel MF, Wanders RJ, Dekker C, Kerckaert IO, Roels F. Van Acker KJ, et al. Among authors: espeel mf. Kidney Int. 1996 Nov;50(5):1747-52. doi: 10.1038/ki.1996.494. Kidney Int. 1996. PMID: 8914045 Free article.

10

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. Among authors: espeel m. Biochimie. 1993;75(3-4):281-92. doi: 10.1016/0300-9084(93)90088-a. Biochimie. 1993. PMID: 7685191 Review.

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