Anvret M - Search Results

1

Mutation screening in Rett syndrome patients.

Xiang F, Buervenich S, Nicolao P, Bailey ME, Zhang Z, Anvret M. Xiang F, et al. Among authors: anvret m. J Med Genet. 2000 Apr;37(4):250-5. doi: 10.1136/jmg.37.4.250. J Med Genet. 2000. PMID: 10745042 Free PMC article.

2

Current status of genetic research in Rett syndrome.

Anvret M, Zhang ZP. Anvret M, et al. Neuropediatrics. 1995 Apr;26(2):88-9. doi: 10.1055/s-2007-979733. Neuropediatrics. 1995. PMID: 7566463

3

Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq.

Xiang F, Zhang Z, Clarke A, Joseluiz P, Sakkubai N, Sarojini B, Delozier-Blanchet CD, Hansmann I, Edström L, Anvret M. Xiang F, et al. Among authors: anvret m. J Med Genet. 1998 Apr;35(4):297-300. doi: 10.1136/jmg.35.4.297. J Med Genet. 1998. PMID: 9598723 Free PMC article.

4

NURR1 mutations in cases of schizophrenia and manic-depressive disorder.

Buervenich S, Carmine A, Arvidsson M, Xiang F, Zhang Z, Sydow O, Jönsson EG, Sedvall GC, Leonard S, Ross RG, Freedman R, Chowdari KV, Nimgaonkar VL, Perlmann T, Anvret M, Olson L. Buervenich S, et al. Among authors: anvret m. Am J Med Genet. 2000 Dec 4;96(6):808-13. doi: 10.1002/1096-8628(20001204)96:6<808::aid-ajmg23>3.0.co;2-e. Am J Med Genet. 2000. PMID: 11121187

5

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease.

Villard L, Lévy N, Xiang F, Kpebe A, Labelle V, Chevillard C, Zhang Z, Schwartz CE, Tardieu M, Chelly J, Anvret M, Fontès M. Villard L, et al. Among authors: anvret m. J Med Genet. 2001 Jul;38(7):435-42. doi: 10.1136/jmg.38.7.435. J Med Genet. 2001. PMID: 11432961 Free PMC article.

6

Closely related Swedish Rett Syndrome females - none with MECP2 mutation revealed.

Xiang F, Stenbom Y, Anvret M, Hagberg B. Xiang F, et al. Among authors: anvret m. Neuropediatrics. 2001 Aug;32(4):217-8. doi: 10.1055/s-2001-17377. Neuropediatrics. 2001. PMID: 11571704

7

Rett syndrome: the bcl-2 gene--a mediator of neurotrophic mechanisms?

Anvret M, Zhang ZP, Hagberg B. Anvret M, et al. Neuropediatrics. 1994 Dec;25(6):323-4. doi: 10.1055/s-2008-1073047. Neuropediatrics. 1994. PMID: 7770130

8

A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.

Xiang F, Almqvist EW, Huq M, Lundin A, Hayden MR, Edström L, Anvret M, Zhang Z. Xiang F, et al. Among authors: anvret m. Am J Hum Genet. 1998 Nov;63(5):1431-8. doi: 10.1086/302093. Am J Hum Genet. 1998. PMID: 9792871 Free PMC article.

9

Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q.

Nicolao P, Xiang F, Gunnarsson LG, Giometto B, Edström L, Anvret M, Zhang Z. Nicolao P, et al. Among authors: anvret m. Am J Hum Genet. 1999 Mar;64(3):788-92. doi: 10.1086/302281. Am J Hum Genet. 1999. PMID: 10053013 Free PMC article.

10

A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21.

Xiang F, Nicolao P, Chapon F, Edström L, Anvret M, Zhang Z. Xiang F, et al. Among authors: anvret m. Neuromuscul Disord. 1999 Jul;9(5):308-12. doi: 10.1016/s0960-8966(99)00030-9. Neuromuscul Disord. 1999. PMID: 10407851

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