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

Year Number of Results
1979 1
1980 2
1983 1
1985 1
1986 1
1989 2
1990 1
1996 1
2000 2
2002 2
2003 3
2004 3
2005 3
2006 7
2007 4
2008 7
2009 6
2010 9
2011 6
2012 1
2013 2
2014 5
2015 7
2016 7
2017 1
2018 8
2019 3
2020 2
2021 4
2022 5
2023 3
2024 2

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102 results

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Page 1
Distal hereditary motor neuropathies.
Tazir M, Nouioua S. Tazir M, et al. Rev Neurol (Paris). 2024 May 2:S0035-3787(23)01111-6. doi: 10.1016/j.neurol.2023.09.005. Online ahead of print. Rev Neurol (Paris). 2024. PMID: 38702287 Review.
Autosomal-recessive Charcot-Marie-Tooth diseases.
Vallat JM, Tazir M, Magdelaine C, Sturtz F, Grid D. Vallat JM, et al. Among authors: tazir m. 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: tazir m. J Neuropathol Exp Neurol. 2018 Feb 1;77(2):88-99. doi: 10.1093/jnen/nlx111. J Neuropathol Exp Neurol. 2018. PMID: 29300988 Review.
[Hereditary peripheral neuropathies].
Vallat JM, Tazir M, Calvo J, Funalot B. Vallat JM, et al. Among authors: tazir m. 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.
Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling.
Schuermans N, El Chehadeh S, Hemelsoet D, Gautheron J, Vantyghem MC, Nouioua S, Tazir M, Vigouroux C, Auclair M, Bogaert E, Dufour S, Okawa F, Hilbert P, Van Doninck N, Taquet MC, Rosseel T, De Clercq G, Debackere E, Van Haverbeke C, Cherif FR, Urtizberea JA, Chanson JB, Funalot B, Authier FJ, Kaya S, Terryn W, Callens S, Depypere B, Van Dorpe J; Program for Undiagnosed Diseases (UD-PrOZA); Poppe B, Impens F, Mizushima N, Depienne C, Jéru I, Dermaut B. Schuermans N, et al. Among authors: tazir m. Nat Genet. 2023 Nov;55(11):1929-1940. doi: 10.1038/s41588-023-01535-3. Epub 2023 Nov 2. Nat Genet. 2023. PMID: 37919452
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease.
Dubourg O, Azzedine H, Verny C, Durosier G, Birouk N, Gouider R, Salih M, Bouhouche A, Thiam A, Grid D, Mayer M, Ruberg M, Tazir M, Brice A, LeGuern E. Dubourg O, et al. Among authors: tazir m. Neuromolecular Med. 2006;8(1-2):75-86. doi: 10.1385/nmm:8:1-2:75. Neuromolecular Med. 2006. PMID: 16775368 Review.
102 results