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Author/Creator Brice, A

4. C06 The β-catenin repressor GSK-3β is a modifier of age at onset in Huntington's disease. (16th November 2010)

Authors:
Parker, J A; Tourette, C; Offner, N; Vazquez-Manrique, R; Mukhopadhyay, A; Darbois, A; Menet, S; Dolbeau, G; Schwenke, S; Maison, P; Orth, M; Brice, A; Dürr, A; Bachoud-Lévi, A-C; Tissenbaum, H A; Néri, C
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 81(2010)Supplement 1
Page Start:
A17
Record Type:
Journal Article
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5. De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group. Issue 8 (August 1998)

Authors:
Dumanchin, C; Brice, A; Campion, D; Hannequin, D; Martin, C; Moreau, V; Agid, Y; Martinez, M; Clerget-Darpoux, F; Frebourg, T
Journal:
Journal of medical genetics
Issue:
Volume 35:Issue 8(1998)
Page Start:
672
Record Type:
Journal Article
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7. Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes. Issue 5 (14th October 2005)

Authors:
Tezenas du Montcel, S; Clot, F; Vidailhet, M; Roze, E; Damier, P; Jedynak, C P; Camuzat, A; Lagueny, A; Vercueil, L; Doummar, D; Guyant-Maréchal, L; Houeto, J-L; Ponsot, G; Thobois, S; Cournelle, M-A; Durr, A; Durif, F; Echenne, B; Hannequin, D; Tranchant, C
Other Names:
group-author.
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 5(2006)
Page Start:
394
Record Type:
Journal Article
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9. Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease. Issue 12 (9th December 2004)

Authors:
Martinez, M; Brice, A; Vaughan, J R; Zimprich, A; Breteler, M M B; Meco, G; Filla, A; Farrer, M J; Bétard, C; Hardy, J; De Michele, G; Bonifati, V; Oostra, B; Gasser, T; Wood, N W; Dürr, A
Other Names:
group-author.
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 12(2004)
Page Start:
900
Record Type:
Journal Article
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10. Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease. Issue 7 (8th April 2009)

Authors:
Lesage, S; Condroyer, C; Lannuzel, A; Lohmann, E; Troiano, A; Tison, F; Damier, P; Thobois, S; Ouvrard-Hernandez, A-M; Rivaud-Péchoux, S; Brefel-Courbon, C; Destée, A; Tranchant, C; Romana, M; Leclere, L; Dürr, A; Brice, A
Journal:
Journal of medical genetics
Issue:
Volume 46:Issue 7(2009)
Page Start:
458
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗