Funalot B - Search Results

1

Peripheral myelin protein 22 gene duplication with atypical presentations: a new example of the wide spectrum of Charcot-Marie-Tooth 1A disease.

Mathis S, Corcia P, Tazir M, Camu W, Magdelaine C, Latour P, Biberon J, Guennoc AM, Richard L, Magy L, Funalot B, Vallat JM. Mathis S, et al. Among authors: funalot b. Neuromuscul Disord. 2014 Jun;24(6):524-8. doi: 10.1016/j.nmd.2014.03.014. Epub 2014 Apr 13. Neuromuscul Disord. 2014. PMID: 24792522

2

[Hereditary peripheral neuropathies].

Vallat JM, Tazir M, Calvo J, Funalot B. Vallat JM, et al. Among authors: funalot b. Presse Med. 2009 Sep;38(9):1325-34. doi: 10.1016/j.lpm.2009.01.014. Epub 2009 Mar 26. Presse Med. 2009. PMID: 19327944 Review. French.

3

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

4

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

5

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

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

6

Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes.

Nouioua S, Hamadouche T, Funalot B, Bernard R, Bellatache N, Bouderba R, Grid D, Assami S, Benhassine T, Levy N, Vallat JM, Tazir M. Nouioua S, et al. Among authors: funalot b. Neuromuscul Disord. 2011 Aug;21(8):543-50. doi: 10.1016/j.nmd.2011.04.013. Epub 2011 Jul 7. Neuromuscul Disord. 2011. PMID: 21741241

7

The various Charcot-Marie-Tooth diseases.

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

8

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: funalot b. J Peripher Nerv Syst. 2013 Sep;18(3):261-5. doi: 10.1111/jns5.12039. J Peripher Nerv Syst. 2013. PMID: 24028195

9

Neuropathologic characterization of INF2-related Charcot-Marie-Tooth disease: evidence for a Schwann cell actinopathy.

Mathis S, Funalot B, Boyer O, Lacroix C, Marcorelles P, Magy L, Richard L, Antignac C, Vallat JM. Mathis S, et al. Among authors: funalot b. J Neuropathol Exp Neurol. 2014 Mar;73(3):223-33. doi: 10.1097/NEN.0000000000000047. J Neuropathol Exp Neurol. 2014. PMID: 24487800

10

Nerve biopsy: requirements for diagnosis and clinical value.

Vallat JM, Funalot B, Magy L. Vallat JM, et al. Among authors: funalot b. Acta Neuropathol. 2011 Mar;121(3):313-26. doi: 10.1007/s00401-011-0804-4. Epub 2011 Feb 4. Acta Neuropathol. 2011. PMID: 21293868 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

109 results

Search Page