Vallat JM - Search Results

1

A highly specific microarray method for point mutation detection.

Baaj Y, Magdelaine C, Ubertelli V, Valat C, Talini L, Soussaline F, Khomyakova E, Funalot B, Vallat JM, Sturtz FG. Baaj Y, et al. Among authors: vallat jm. Biotechniques. 2008 Jan;44(1):119-26. doi: 10.2144/000112630. Biotechniques. 2008. PMID: 18254389 Free article.

2

Multiplex detection and genotyping of point mutations involved in charcot-marie-tooth disease using a hairpin microarray-based assay.

Baaj Y, Magdelaine C, Ubertelli V, Valat C, Mousseau Y, Qiu H, Funalot B, Vallat JM, Sturtz FG. Baaj Y, et al. Among authors: vallat jm. Res Lett Biochem. 2009;2009:960560. doi: 10.1155/2009/960560. Epub 2009 Jun 11. Res Lett Biochem. 2009. PMID: 22820753 Free PMC article.

3

Autosomal-recessive Charcot-Marie-Tooth diseases.

Vallat JM, Tazir M, Magdelaine C, Sturtz F, Grid D. Vallat JM, et al. J Neuropathol Exp Neurol. 2005 May;64(5):363-70. doi: 10.1093/jnen/64.5.363. J Neuropathol Exp Neurol. 2005. PMID: 15892292 Review.

4

[Ultrastructural lesions of axonal mitochondria in patients with childhood-onset Charcot-Marie-Tooth disease due to MFN2 mutations].

Funalot B, Magdelaine C, Sturtz F, Ouvrier R, Vallat JM. Funalot B, et al. Among authors: vallat jm. Bull Acad Natl Med. 2009 Jan;193(1):151-60; discussion 160-1. Bull Acad Natl Med. 2009. PMID: 19718987 French.

5

Genotype-phenotype correlations in Charcot-Marie-Tooth disease type 2 caused by mitofusin 2 mutations.

Calvo J, Funalot B, Ouvrier RA, Lazaro L, Toutain A, De Mas P, Bouche P, Gilbert-Dussardier B, Arne-Bes MC, Carrière JP, Journel H, Minot-Myhie MC, Guillou C, Ghorab K, Magy L, Sturtz F, Vallat JM, Magdelaine C. Calvo J, et al. Among authors: vallat jm. Arch Neurol. 2009 Dec;66(12):1511-6. doi: 10.1001/archneurol.2009.284. Arch Neurol. 2009. PMID: 20008656

6

[Charcot-Marie-Tooth (CMT) disease: an update].

Vallat JM, Funalot B. Vallat JM, et al. Med Sci (Paris). 2010 Oct;26(10):842-7. doi: 10.1051/medsci/20102610842. Med Sci (Paris). 2010. PMID: 20929675 Free article. Review. French.

7

Homozygous deletion of an EGR2 enhancer in congenital amyelinating neuropathy.

Funalot B, Topilko P, Arroyo MA, Sefiani A, Hedley-Whyte ET, Yoldi ME, Richard L, Touraille E, Laurichesse M, Khalifa E, Chauzeix J, Ouedraogo A, Cros D, Magdelaine C, Sturtz FG, Urtizberea JA, Charnay P, Bragado FG, Vallat JM. Funalot B, et al. Among authors: vallat jm. Ann Neurol. 2012 May;71(5):719-23. doi: 10.1002/ana.23527. Ann Neurol. 2012. PMID: 22522483

8

The various Charcot-Marie-Tooth diseases.

Vallat JM, Mathis S, Funalot B. Vallat JM, et al. Curr Opin Neurol. 2013 Oct;26(5):473-80. doi: 10.1097/WCO.0b013e328364c04b. Curr Opin Neurol. 2013. PMID: 23945280 Review.

9

CMT4D (NDRG1 mutation): genotype-phenotype correlations.

Ricard E, Mathis S, Magdelaine C, Delisle MB, Magy L, Funalot B, Vallat JM. Ricard E, et al. Among authors: vallat jm. J Peripher Nerv Syst. 2013 Sep;18(3):261-5. doi: 10.1111/jns5.12039. J Peripher Nerv Syst. 2013. PMID: 24028195

10

[Autosomal recessive forms of Charcot-Marie-Tooth disease].

Vallat JM, Grid D, Magdelaine C, Sturtz F, Levy N, Tazir M. Vallat JM, et al. Bull Acad Natl Med. 2005 Jan;189(1):55-68; discussion 68-9. Bull Acad Natl Med. 2005. PMID: 16119880 Review. French.

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