Sanson M - Search Results

1

Mutational analysis of the PTEN gene in gliomas: molecular and pathological correlations.

Zhou XP, Li YJ, Hoang-Xuan K, Laurent-Puig P, Mokhtari K, Longy M, Sanson M, Delattre JY, Thomas G, Hamelin R. Zhou XP, et al. Among authors: sanson m. Int J Cancer. 1999 Apr 20;84(2):150-4. doi: 10.1002/(sici)1097-0215(19990420)84:2<150::aid-ijc10>3.0.co;2-#. Int J Cancer. 1999. PMID: 10096247

2

Allelic loss on chromosome 22 correlates with histopathological predictors of recurrence of meningiomas.

Sanson M, Richard S, Delattre O, Poliwka M, Mikol J, Philippon J, Thomas G. Sanson M, et al. Int J Cancer. 1992 Feb 1;50(3):391-4. doi: 10.1002/ijc.2910500311. Int J Cancer. 1992. PMID: 1346529

3

Screening for germ-line mutations in the NF2 gene.

Mérel P, Hoang-Xuan K, Sanson M, Bijlsma E, Rouleau G, Laurent-Puig P, Pulst S, Baser M, Lenoir G, Sterkers JM, et al. Mérel P, et al. Among authors: sanson m. Genes Chromosomes Cancer. 1995 Feb;12(2):117-27. doi: 10.1002/gcc.2870120206. Genes Chromosomes Cancer. 1995. PMID: 7535084

4

Genetic alterations in the chromosome 22q12 region associated with development of neuroectodermal tumors.

Thomas G, Delattre O, Zucman J, Merel P, Desmaze C, Melot T, Sanson M, Hoang-Xuan K, Plougastel B, Dejong P, et al. Thomas G, et al. Among authors: sanson m. Cold Spring Harb Symp Quant Biol. 1994;59:555-64. doi: 10.1101/sqb.1994.059.01.062. Cold Spring Harb Symp Quant Biol. 1994. PMID: 7587112 No abstract available.

5

Predominant occurrence of somatic mutations of the NF2 gene in meningiomas and schwannomas.

Mérel P, Hoang-Xuan K, Sanson M, Moreau-Aubry A, Bijlsma EK, Lazaro C, Moisan JP, Resche F, Nishisho I, Estivill X, et al. Mérel P, et al. Among authors: sanson m. Genes Chromosomes Cancer. 1995 Jul;13(3):211-6. doi: 10.1002/gcc.2870130311. Genes Chromosomes Cancer. 1995. PMID: 7669741

6

[Peripheral neurological complications of Epstein-Barr virus infection].

Thibault JL, Mercier B, Roos-Weil R, Sanson M, Delattre JY. Thibault JL, et al. Among authors: sanson m. Rev Neurol (Paris). 1995 Feb;151(2):142-4. Rev Neurol (Paris). 1995. PMID: 7676144 French.

7

Neurofibromatosis type 2.

Thomas G, Mérel P, Sanson M, Hoang-Xuan K, Zucman J, Desmaze C, Melot T, Aurias A, Delattre O. Thomas G, et al. Among authors: sanson m. Eur J Cancer. 1994;30A(13):1981-7. doi: 10.1016/0959-8049(94)00390-q. Eur J Cancer. 1994. PMID: 7734211 Review. No abstract available.

8

[Primary meningeal gliomatosis].

Carpentier AF, Sanson M, Kujas M, Giroud M, Poisson M, Delattre JY. Carpentier AF, et al. Among authors: sanson m. Rev Neurol (Paris). 1994;150(3):232-5. Rev Neurol (Paris). 1994. PMID: 7863170 French.

9

Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization.

Demczuk S, Desmaze C, Aikem M, Prieur M, Ledeist F, Sanson M, Rouleau G, Thomas G, Aurias A. Demczuk S, et al. Among authors: sanson m. Ann Genet. 1994;37(2):60-5. Ann Genet. 1994. PMID: 7985979

10

The neurofibromatosis type 2 gene is inactivated in schwannomas.

Twist EC, Ruttledge MH, Rousseau M, Sanson M, Papi L, Merel P, Delattre O, Thomas G, Rouleau GA. Twist EC, et al. Among authors: sanson m. Hum Mol Genet. 1994 Jan;3(1):147-51. doi: 10.1093/hmg/3.1.147. Hum Mol Genet. 1994. PMID: 8162016

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