Mignot C - Search Results

1

A Novel Homozygous TBC1D24 Mutation Causing Multifocal Myoclonus With Cerebellar Involvement.

Doummar D, Mignot C, Apartis E, Villard L, Rodriguez D, Chantot-Bastauraud S, Burglen L. Doummar D, et al. Among authors: mignot c. Mov Disord. 2015 Sep;30(10):1431-2. doi: 10.1002/mds.26303. Epub 2015 Jul 24. Mov Disord. 2015. PMID: 26207815 No abstract available.

2

Alexander disease: putative mechanisms of an astrocytic encephalopathy.

Mignot C, Boespflug-Tanguy O, Gelot A, Dautigny A, Pham-Dinh D, Rodriguez D. Mignot C, et al. Cell Mol Life Sci. 2004 Feb;61(3):369-85. doi: 10.1007/s00018-003-3143-3. Cell Mol Life Sci. 2004. PMID: 14770299 Free PMC article. Review.

3

Myoclonus and generalized digestive dysmotility in triple A syndrome with AAAS gene mutation.

Roubergue A, Apartis E, Vidailhet M, Mignot C, Tullio-Pelet A, Lyonnet S, de Villemeur TB. Roubergue A, et al. Among authors: mignot c. Mov Disord. 2004 Mar;19(3):344-6. doi: 10.1002/mds.10660. Mov Disord. 2004. PMID: 15022193

4

[Fetal neurology: conditions of diagnostic uncertainty].

Moutard ML, Gélot A, Rodriguez D, Guët A, Mignot C, Ponsot G, Billette de Villemeur T. Moutard ML, et al. Among authors: mignot c. Arch Pediatr. 2006 Jun;13(6):825-7. doi: 10.1016/j.arcped.2006.03.128. Epub 2006 May 12. Arch Pediatr. 2006. PMID: 16698255 French. No abstract available.

5

[Human herpes virus type 6, etiology of an acute encephalitis in childhood: case report].

Afenjar A, Rodriguez D, Rozenberg F, Dorison N, Guët A, Mignot C, Doummar D, Billette de Villemeur T, Ponsot G. Afenjar A, et al. Among authors: mignot c. Arch Pediatr. 2007 May;14(5):472-5. doi: 10.1016/j.arcped.2006.12.020. Epub 2007 Feb 15. Arch Pediatr. 2007. PMID: 17306516 French.

6

Early neurological phenotype in 4 children with biallelic PRODH mutations.

Afenjar A, Moutard ML, Doummar D, Guët A, Rabier D, Vermersch AI, Mignot C, Burglen L, Heron D, Thioulouse E, de Villemeur TB, Campion D, Rodriguez D. Afenjar A, et al. Among authors: mignot c. Brain Dev. 2007 Oct;29(9):547-52. doi: 10.1016/j.braindev.2007.01.008. Epub 2007 Apr 6. Brain Dev. 2007. PMID: 17412540

7

Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander disease.

Mignot C, Delarasse C, Escaich S, Della Gaspera B, Noé E, Colucci-Guyon E, Babinet C, Pekny M, Vicart P, Boespflug-Tanguy O, Dautigny A, Rodriguez D, Pham-Dinh D. Mignot C, et al. Exp Cell Res. 2007 Aug 1;313(13):2766-79. doi: 10.1016/j.yexcr.2007.04.035. Epub 2007 May 24. Exp Cell Res. 2007. PMID: 17604020

8

Progressive megalencephaly due to specific EIF2Bepsilon mutations in two unrelated families.

Passemard S, Gelot A, Fogli A, N'Guyen S, Barnerias C, Niel F, Doummar D, Arbues AS, Mignot C, de Villemeur TB, Ponsot G, Boespflug-Tanguy O, Rodriguez D. Passemard S, et al. Among authors: mignot c. Neurology. 2007 Jul 24;69(4):400-2. doi: 10.1212/01.wnl.0000266388.02772.f8. Neurology. 2007. PMID: 17646634 No abstract available.

9

Tumor-like enlargement of the optic chiasm in an infant with Alexander disease.

Mignot C, Desguerre I, Burglen L, Hertz-Pannier L, Renaldo F, Gadisseux JF, Gallet S, Pham-Dinh D, Boespflug-Tanguy O, Rodriguez D. Mignot C, et al. Brain Dev. 2009 Mar;31(3):244-7. doi: 10.1016/j.braindev.2008.05.005. Epub 2008 Jun 26. Brain Dev. 2009. PMID: 18584981

10

Infantile hypokinetic-hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene.

Doummar D, Clot F, Vidailhet M, Afenjar A, Durr A, Brice A, Mignot C, Guet A, de Villemeur TB, Rodriguez D. Doummar D, et al. Among authors: mignot c. Mov Disord. 2009 Apr 30;24(6):943-5. doi: 10.1002/mds.22455. Mov Disord. 2009. PMID: 19224593 No abstract available.

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