Magdelaine C - 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: magdelaine c. 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. Among authors: magdelaine c. 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. Among authors: magdelaine c. 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

IgG neuropathy: an immunoelectron microscopic study.

Vallat JM, Magy L, Sindou P, Magdelaine C, Cros D. Vallat JM, et al. Among authors: magdelaine c. J Neuropathol Exp Neurol. 2005 May;64(5):386-90. doi: 10.1093/jnen/64.5.386. J Neuropathol Exp Neurol. 2005. PMID: 15892295

5

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

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

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. Among authors: magdelaine c. 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

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. Among authors: magdelaine c. Neurology. 2008 May 6;70(19):1678-81. doi: 10.1212/01.wnl.0000311275.89032.22. Neurology. 2008. PMID: 18458227

8

Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations.

Vallat JM, Ouvrier RA, Pollard JD, Magdelaine C, Zhu D, Nicholson GA, Grew S, Ryan MM, Funalot B. Vallat JM, et al. Among authors: magdelaine c. J Neuropathol Exp Neurol. 2008 Nov;67(11):1097-102. doi: 10.1097/NEN.0b013e31818b6cbc. J Neuropathol Exp Neurol. 2008. PMID: 18957892

9

[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: magdelaine c. Bull Acad Natl Med. 2009 Jan;193(1):151-60; discussion 160-1. Bull Acad Natl Med. 2009. PMID: 19718987 French.

10

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: magdelaine c. Arch Neurol. 2009 Dec;66(12):1511-6. doi: 10.1001/archneurol.2009.284. Arch Neurol. 2009. PMID: 20008656

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