Aubourg P - Search Results

1

Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two cases.

Rodriguez D, Gelot A, della Gaspera B, Robain O, Ponsot G, Sarliève LL, Ghandour S, Pompidou A, Dautigny A, Aubourg P, Pham-Dinh D. Rodriguez D, et al. Among authors: aubourg p. Acta Neuropathol. 1999 May;97(5):469-80. doi: 10.1007/s004010051016. Acta Neuropathol. 1999. PMID: 10334484

2

Menkes disease: a Golgi and electron microscopic study of the cerebellar cortex.

Robain O, Aubourg P, Routon MC, Dulac O, Ponsot G. Robain O, et al. Among authors: aubourg p. Clin Neuropathol. 1988 Mar-Apr;7(2):47-52. Clin Neuropathol. 1988. PMID: 3390973

3

Expression of the adrenoleukodystrophy protein in the human and mouse central nervous system.

Fouquet F, Zhou JM, Ralston E, Murray K, Troalen F, Magal E, Robain O, Dubois-Dalcq M, Aubourg P. Fouquet F, et al. Among authors: aubourg p. Neurobiol Dis. 1997;3(4):271-85. doi: 10.1006/nbdi.1997.0127. Neurobiol Dis. 1997. PMID: 9173925

4

Apoptosis in the central nervous system of cerebral adrenoleukodystrophy patients.

Feigenbaum V, Gélot A, Casanova P, Daumas-Duport C, Aubourg P, Dubois-Dalcq M. Feigenbaum V, et al. Among authors: aubourg p. Neurobiol Dis. 2000 Dec;7(6 Pt B):600-12. doi: 10.1006/nbdi.2000.0315. Neurobiol Dis. 2000. PMID: 11114259

5

The cerebro-hepato-renal (Zellweger) syndrome: lamellar lipid profiles in adrenocortical, hepatic mesenchymal, astrocyte cells and increased levels of very long chain fatty acids and phytanic acid in the plasma.

Aubourg P, Robain O, Rocchiccioli F, Dancea S, Scotto J. Aubourg P, et al. J Neurol Sci. 1985 May-Jun;69(1-2):9-25. doi: 10.1016/0022-510x(85)90003-6. J Neurol Sci. 1985. PMID: 4009207

6

Case definition and classification of leukodystrophies and leukoencephalopathies.

Vanderver A, Prust M, Tonduti D, Mochel F, Hussey HM, Helman G, Garbern J, Eichler F, Labauge P, Aubourg P, Rodriguez D, Patterson MC, Van Hove JL, Schmidt J, Wolf NI, Boespflug-Tanguy O, Schiffmann R, van der Knaap MS; GLIA Consortium. Vanderver A, et al. Among authors: aubourg p. Mol Genet Metab. 2015 Apr;114(4):494-500. doi: 10.1016/j.ymgme.2015.01.006. Epub 2015 Jan 29. Mol Genet Metab. 2015. PMID: 25649058 Free PMC article. Review.

7

Neonatal adrenoleukodystrophy.

Aubourg P, Scotto J, Rocchiccioli F, Feldmann-Pautrat D, Robain O. Aubourg P, et al. J Neurol Neurosurg Psychiatry. 1986 Jan;49(1):77-86. doi: 10.1136/jnnp.49.1.77. J Neurol Neurosurg Psychiatry. 1986. PMID: 2420940 Free PMC article.

8

[Lyme disease. Apropos of a case in children].

Moutard ML, Aubourg P, Mayer M, Dournon E, Ponsot G. Moutard ML, et al. Among authors: aubourg p. Arch Fr Pediatr. 1986 Nov;43(9):705-7. Arch Fr Pediatr. 1986. PMID: 3813800 French.

9

[MRI and metabolic brain pathology].

Adamsbaum C, Aubourg P. Adamsbaum C, et al. Among authors: aubourg p. JBR-BTR. 2005 Sep-Oct;88(5):249-50. JBR-BTR. 2005. PMID: 16302338 French. No abstract available.

10

X-linked adrenoleukodystrophy enigma: how does the ALD peroxisomal transporter mutation affect CNS glia?

Aubourg P, Dubois-Dalcq M. Aubourg P, et al. Glia. 2000 Jan 15;29(2):186-90. doi: 10.1002/(sici)1098-1136(20000115)29:2<186::aid-glia13>3.0.co;2-5. Glia. 2000. PMID: 10625338 Review. No abstract available.

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