Delisle MB - Search Results

1

Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family.

Tsuboi Y, Uitti RJ, Delisle MB, Ferreira JJ, Brefel-Courbon C, Rascol O, Ghetti B, Murrell JR, Hutton M, Baker M, Wszolek ZK. Tsuboi Y, et al. Among authors: delisle mb. Arch Neurol. 2002 Jun;59(6):943-50. doi: 10.1001/archneur.59.6.943. Arch Neurol. 2002. PMID: 12056930

2

The effect of tau genotype on clinical features in FTDP-17.

Baba Y, Tsuboi Y, Baker MC, Uitti RJ, Hutton ML, Dickson DW, Farrer M, Putzke JD, Woodruff BK, Ghetti B, Murrell JR, Boeve BF, Petersen RC, Verpillat P, Brice A, Delisle MB, Rascol O, Arima K, Dysken MW, Yasuda M, Kobayashi T, Sunohara N, Komure O, Kuno S, Sperfeld AD, Stoppe G, Kohlhase J, Pickering-Brown S, Neary D, Bugiani O, Wszolek ZK. Baba Y, et al. Among authors: delisle mb. Parkinsonism Relat Disord. 2005 Jun;11(4):205-8. doi: 10.1016/j.parkreldis.2005.01.003. Parkinsonism Relat Disord. 2005. PMID: 15878580

3

[Neurodegenerative disease associated with a mutation of codon 279 (N279K) in exon 10 of Tau protein].

Delisle MB, Uro-Coste E, Murrell JR, Rascol O, Ghetti B. Delisle MB, et al. Bull Acad Natl Med. 2000;184(4):799-809; discussion 809-11. Bull Acad Natl Med. 2000. PMID: 10989564 Review. French.

4

A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy.

Delisle MB, Murrell JR, Richardson R, Trofatter JA, Rascol O, Soulages X, Mohr M, Calvas P, Ghetti B. Delisle MB, et al. Acta Neuropathol. 1999 Jul;98(1):62-77. doi: 10.1007/s004010051052. Acta Neuropathol. 1999. PMID: 10412802

5

Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene.

Vidal R, Ghetti B, Takao M, Brefel-Courbon C, Uro-Coste E, Glazier BS, Siani V, Benson MD, Calvas P, Miravalle L, Rascol O, Delisle MB. Vidal R, et al. Among authors: delisle mb. J Neuropathol Exp Neurol. 2004 Apr;63(4):363-80. doi: 10.1093/jnen/63.4.363. J Neuropathol Exp Neurol. 2004. PMID: 15099026

6

Neurodegeneration caused by proteins with an aberrant carboxyl-terminus.

Vidal R, Delisle MB, Ghetti B. Vidal R, et al. Among authors: delisle mb. J Neuropathol Exp Neurol. 2004 Aug;63(8):787-800. doi: 10.1093/jnen/63.8.787. J Neuropathol Exp Neurol. 2004. PMID: 15330334 Review.

7

Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease.

Shiarli AM, Jennings R, Shi J, Bailey K, Davidson Y, Tian J, Bigio EH, Ghetti B, Murrell JR, Delisle MB, Mirra S, Crain B, Zolo P, Arima K, Iseki E, Murayama S, Kretzschmar H, Neumann M, Lippa C, Halliday G, Mackenzie J, Khan N, Ravid R, Dickson D, Wszolek Z, Iwatsubo T, Pickering-Brown SM, Mann DM. Shiarli AM, et al. Among authors: delisle mb. Neuropathol Appl Neurobiol. 2006 Aug;32(4):374-87. doi: 10.1111/j.1365-2990.2006.00736.x. Neuropathol Appl Neurobiol. 2006. PMID: 16866983

8

Activation of the JNK/p38 pathway occurs in diseases characterized by tau protein pathology and is related to tau phosphorylation but not to apoptosis.

Atzori C, Ghetti B, Piva R, Srinivasan AN, Zolo P, Delisle MB, Mirra SS, Migheli A. Atzori C, et al. Among authors: delisle mb. J Neuropathol Exp Neurol. 2001 Dec;60(12):1190-7. doi: 10.1093/jnen/60.12.1190. J Neuropathol Exp Neurol. 2001. PMID: 11764091

9

Encephalopathy with neuroserpin inclusion bodies presenting as progressive myoclonus epilepsy and associated with a novel mutation in the Proteinase Inhibitor 12 gene.

Hagen MC, Murrell JR, Delisle MB, Andermann E, Andermann F, Guiot MC, Ghetti B. Hagen MC, et al. Among authors: delisle mb. Brain Pathol. 2011 Sep;21(5):575-82. doi: 10.1111/j.1750-3639.2011.00481.x. Epub 2011 Mar 24. Brain Pathol. 2011. PMID: 21435071 Free PMC article.

10

Hereditary ferritinopathy.

Vidal R, Delisle MB, Rascol O, Ghetti B. Vidal R, et al. Among authors: delisle mb. J Neurol Sci. 2003 Mar 15;207(1-2):110-1. doi: 10.1016/s0022-510x(02)00435-5. J Neurol Sci. 2003. PMID: 12614943 Review. No abstract available.

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