Sturtz FG - 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: sturtz fg. Biotechniques. 2008 Jan;44(1):119-26. doi: 10.2144/000112630. Biotechniques. 2008. PMID: 18254389 Free article.

2

Autosomal recessive forms of Charcot-Marie-Tooth disease.

Vallat JM, Grid D, Magdelaine C, Sturtz F, Tazir M. Vallat JM, et al. Curr Neurol Neurosci Rep. 2004 Sep;4(5):413-9. Curr Neurol Neurosci Rep. 2004. PMID: 15324608

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

[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.

5

Contribution of electron microscopy to the study of neuropathies associated with an IgG monoclonal paraproteinemia.

Vallat JM, Magy L, Richard L, Sturtz F, Couratier P. Vallat JM, et al. Micron. 2008;39(2):61-70. doi: 10.1016/j.micron.2006.12.005. Epub 2007 Jan 13. Micron. 2008. PMID: 17291771 Review.

6

Diagnostic value of ultrastructural nerve examination in Charcot-Marie-Tooth disease: two CMT 1B cases with pseudo-recessive inheritance.

Vallat JM, Magy L, Lagrange E, Sturtz F, Magdelaine C, Grid D, Tazir M. Vallat JM, et al. Acta Neuropathol. 2007 Apr;113(4):443-9. doi: 10.1007/s00401-007-0196-7. Epub 2007 Feb 10. Acta Neuropathol. 2007. PMID: 17294201

7

Gene expression of HIF-1alpha and XRCC4 measured in human samples by real-time RT-PCR using the sigmoidal curve-fitting method.

Qiu H, Durand K, Rabinovitch-Chable H, Rigaud M, Gazaille V, Clavère P, Sturtz FG. Qiu H, et al. Among authors: sturtz fg. Biotechniques. 2007 Mar;42(3):355-62. doi: 10.2144/000112331. Biotechniques. 2007. PMID: 17390542 Free article.

8

Improved agarose gel assay for quantification of growth factor-induced cell motility.

Mousseau Y, Leclers D, Faucher-Durand K, Cook-Moreau J, Lia-Baldini AS, Rigaud M, Sturtz FG. Mousseau Y, et al. Among authors: sturtz fg. Biotechniques. 2007 Oct;43(4):509-16. doi: 10.2144/000112557. Biotechniques. 2007. PMID: 18019343 Free article.

9

Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations.

Nicholson GA, Magdelaine C, Zhu D, Grew S, Ryan MM, Sturtz F, Vallat JM, Ouvrier RA. Nicholson GA, et al. Neurology. 2008 May 6;70(19):1678-81. doi: 10.1212/01.wnl.0000311275.89032.22. Neurology. 2008. PMID: 18458227

10

High metabolic level in patients with familial amyotrophic lateral sclerosis.

Funalot B, Desport JC, Sturtz F, Camu W, Couratier P. Funalot B, et al. Amyotroph Lateral Scler. 2009 Apr;10(2):113-7. doi: 10.1080/17482960802295192. Amyotroph Lateral Scler. 2009. PMID: 18792852

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