Robain O - Search Results

1

Iatrogenic Creutzfeldt-Jakob disease in three growth hormone recipients: a neuropathological study.

Billette de Villemeur T, Gelot A, Deslys JP, Dormont D, Duyckaerts C, Jardin L, Denni J, Robain O. Billette de Villemeur T, et al. Among authors: robain o. Neuropathol Appl Neurobiol. 1994 Apr;20(2):111-7. doi: 10.1111/j.1365-2990.1994.tb01169.x. Neuropathol Appl Neurobiol. 1994. PMID: 8072642

2

Value of magnetic resonance imaging in West syndrome of unknown etiology.

van Bogaert P, Chiron C, Adamsbaum C, Robain O, Diebler C, Dulac O. van Bogaert P, et al. Among authors: robain o. Epilepsia. 1993 Jul-Aug;34(4):701-6. doi: 10.1111/j.1528-1157.1993.tb00449.x. Epilepsia. 1993. PMID: 8330581

3

Familial occurrence of prenatal encephaloclastic damage: anatomoclinical report of 2 cases.

Bordarier C, Robain O. Bordarier C, et al. Among authors: robain o. Neuropediatrics. 1989 May;20(2):103-6. doi: 10.1055/s-2008-1071274. Neuropediatrics. 1989. PMID: 2739873

4

Ultrastructural localization of cellular prion protein (PrPc) in synaptic boutons of normal hamster hippocampus.

Fournier JG, Escaig-Haye F, Billette de Villemeur T, Robain O. Fournier JG, et al. Among authors: robain o. C R Acad Sci III. 1995 Mar;318(3):339-44. C R Acad Sci III. 1995. PMID: 7788502

5

Cardiac rhabdomyoma and tuberous sclerosis in three fetuses: a neuropathological study.

Bordarier C, Lellouch-Tubiana A, Robain O. Bordarier C, et al. Among authors: robain o. Brain Dev. 1994 Nov-Dec;16(6):467-71. doi: 10.1016/0387-7604(94)90010-8. Brain Dev. 1994. PMID: 7694997

6

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. Clin Neuropathol. 1988 Mar-Apr;7(2):47-52. Clin Neuropathol. 1988. PMID: 3390973

7

Unlayered polymicrogyria and agenesis of the corpus callosum: a relevant association?

Billette de Villemeur T, Chiron C, Robain O. Billette de Villemeur T, et al. Among authors: robain o. Acta Neuropathol. 1992;83(3):265-70. doi: 10.1007/BF00296788. Acta Neuropathol. 1992. PMID: 1557957

8

Clinical, biochemical, and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the mtDNA T8993G point mutation.

Degoul F, Diry M, Rodriguez D, Robain O, Francois D, Ponsot G, Marsac C, Desguerre I. Degoul F, et al. Among authors: robain o. J Inherit Metab Dis. 1995;18(6):682-8. doi: 10.1007/BF02436757. J Inherit Metab Dis. 1995. PMID: 8750605

9

Microgyric and necrotic cortical lesions in twin fetuses: original cerebral damage consecutive to twinning?

Bordarier C, Robain O. Bordarier C, et al. Among authors: robain o. Brain Dev. 1992 May;14(3):174-8. doi: 10.1016/s0387-7604(12)80260-9. Brain Dev. 1992. PMID: 1514658

10

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: robain o. Neurobiol Dis. 1997;3(4):271-85. doi: 10.1006/nbdi.1997.0127. Neurobiol Dis. 1997. PMID: 9173925

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