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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1961 1
2004 1
2005 3
2007 1
2008 4
2009 4
2010 1
2012 2
2013 4
2014 3
2015 1
2016 1
2017 1
2018 4
2019 7
2020 5
2021 4
2022 6
2023 2
2024 0

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52 results

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Page 1
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.
Nerve Biopsy Is Still Useful in Some Inherited Neuropathies.
Duchesne M, Mathis S, Richard L, Magdelaine C, Corcia P, Nouioua S, Tazir M, Magy L, Vallat JM. Duchesne M, et al. Among authors: magdelaine c. J Neuropathol Exp Neurol. 2018 Feb 1;77(2):88-99. doi: 10.1093/jnen/nlx111. J Neuropathol Exp Neurol. 2018. PMID: 29300988 Review.
HINT1 neuropathy: Expanding the genotype and phenotype spectrum.
Morel V, Campana-Salort E, Boyer A, Esselin F, Walther-Louvier U, Querin G, Latour P, Lia AS, Magdelaine C, Beze-Beyrie P, Behin A, Delague V, Levy N, Stojkovic T, Attarian S, Bonello-Palot N. Morel V, et al. Among authors: magdelaine c. Clin Genet. 2022 Nov;102(5):379-390. doi: 10.1111/cge.14198. Epub 2022 Aug 16. Clin Genet. 2022. PMID: 35882622 Free PMC article. Review.
Clinical features of homozygous FIG4-p.Ile41Thr Charcot-Marie-Tooth 4J patients.
Lafontaine M, Lia AS, Bourthoumieu S, Beauvais-Dzugan H, Derouault P, Arné-Bes MC, Sarret C, Laffargue F, Magot A, Sturtz F, Magy L, Magdelaine C. Lafontaine M, et al. Among authors: magdelaine c. Ann Clin Transl Neurol. 2021 Feb;8(2):471-476. doi: 10.1002/acn3.51175. Epub 2021 Jan 6. Ann Clin Transl Neurol. 2021. PMID: 33405357 Free PMC article.
A mutation can hide another one: Think Structural Variants!
Miressi F, Faye PA, Pyromali I, Bourthoumieux S, Derouault P, Husson M, Favreau F, Sturtz F, Magdelaine C, Lia AS. Miressi F, et al. Among authors: magdelaine c. Comput Struct Biotechnol J. 2020 Aug 2;18:2095-2099. doi: 10.1016/j.csbj.2020.07.021. eCollection 2020. Comput Struct Biotechnol J. 2020. PMID: 32832037 Free PMC article.
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: magdelaine c. J Peripher Nerv Syst. 2013 Sep;18(3):261-5. doi: 10.1111/jns5.12039. J Peripher Nerv Syst. 2013. PMID: 24028195
A National French Consensus on Gene List for the Diagnosis of Charcot-Marie-Tooth Disease and Related Disorders Using Next-Generation Sequencing.
Benquey T, Pion E, Cossée M, Krahn M, Stojkovic T, Perrin A, Cerino M, Molon A, Lia AS, Magdelaine C, Francou B, Guiochon-Mantel A, Malinge MC, Leguern E, Lévy N, Attarian S, Latour P, Bonello-Palot N. Benquey T, et al. Among authors: magdelaine c. Genes (Basel). 2022 Feb 9;13(2):318. doi: 10.3390/genes13020318. Genes (Basel). 2022. PMID: 35205364 Free PMC article.
52 results