Saudubray JM - 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: saudubray jm. Ann Neurol. 1998 Nov;44(5):720-30. doi: 10.1002/ana.410440505. Ann Neurol. 1998. PMID: 9818927

2

Clinical approach to inherited peroxisomal disorders.

Poggi-Travert F, Fournier B, Poll-The BT, Saudubray JM. Poggi-Travert F, et al. Among authors: saudubray jm. J Inherit Metab Dis. 1995;18 Suppl 1:1-18. doi: 10.1007/BF00711425. J Inherit Metab Dis. 1995. PMID: 9053544 Review.

3

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: saudubray jm. Neurology. 1998 Nov;51(5):1427-32. doi: 10.1212/wnl.51.5.1427. Neurology. 1998. PMID: 9818873

4

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

5

[Clinical aspects of hereditary peroxisomal disorders].

Billette de Villemeur T, Poll The BT, Saudubray JM. Billette de Villemeur T, et al. Among authors: saudubray jm. Minerva Pediatr. 1991 Mar;43(3):115-23. Minerva Pediatr. 1991. PMID: 1870505 Review. French. No abstract available.

6

Peroxisomal disorders.

Baumgartner MR, Saudubray JM. Baumgartner MR, et al. Among authors: saudubray jm. Semin Neonatol. 2002 Feb;7(1):85-94. doi: 10.1053/siny.2001.0089. Semin Neonatol. 2002. PMID: 12069541 Review.

7

Hyperpipecolic acidaemia: a diagnostic tool for peroxisomal disorders.

Peduto A, Baumgartner MR, Verhoeven NM, Rabier D, Spada M, Nassogne MC, Poll-The BT, Bonetti G, Jakobs C, Saudubray JM. Peduto A, et al. Among authors: saudubray jm. Mol Genet Metab. 2004 Jul;82(3):224-30. doi: 10.1016/j.ymgme.2004.04.010. Mol Genet Metab. 2004. PMID: 15234336

8

Complementation analysis of peroxisomal disorders and classical Refsum.

Poll-The BT, Skjeldal OH, Stokke O, Demaugre F, Saudubray JM. Poll-The BT, et al. Among authors: saudubray jm. Prog Clin Biol Res. 1990;321:537-43. Prog Clin Biol Res. 1990. PMID: 1691507 No abstract available.

9

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: saudubray jm. Virchows Arch A Pathol Anat Histopathol. 1991;419(6):523-5. doi: 10.1007/BF01650683. Virchows Arch A Pathol Anat Histopathol. 1991. PMID: 1750197

10

A new type of chondrodysplasia punctata associated with peroxisomal dysfunction.

Poll-The BT, Maroteaux P, Narcy C, Quetin P, Guesnu M, Wanders RJ, Schutgens RB, Saudubray JM. Poll-The BT, et al. Among authors: saudubray jm. J Inherit Metab Dis. 1991;14(3):361-3. doi: 10.1007/BF01811703. J Inherit Metab Dis. 1991. PMID: 1770792 No abstract available.

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