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

Year Number of Results
1989 2
1991 1
1992 3
1993 4
1994 2
1995 7
1996 2
1997 4
1998 6
1999 3
2000 2
2001 8
2002 3
2003 2
2004 2
2005 3
2006 1
2007 2
2008 1
2009 4
2010 2
2011 3
2012 1
2013 3
2014 2
2015 4
2016 4
2017 4
2018 4
2019 7
2020 11
2022 1
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99 results
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Page 1
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.
Poirier K, Lebrun N, Broix L, Tian G, Saillour Y, Boscheron C, Parrini E, Valence S, Pierre BS, Oger M, Lacombe D, Geneviève D, Fontana E, Darra F, Cances C, Barth M, Bonneau D, Bernadina BD, N'guyen S, Gitiaux C, Parent P, des Portes V, Pedespan JM, Legrez V, Castelnau-Ptakine L, Nitschke P, Hieu T, Masson C, Zelenika D, Andrieux A, Francis F, Guerrini R, Cowan NJ, Bahi-Buisson N, Chelly J. Poirier K, et al. Among authors: pedespan jm. Nat Genet. 2013 Jun;45(6):639-47. doi: 10.1038/ng.2613. Epub 2013 Apr 21. Nat Genet. 2013. PMID: 23603762 Free PMC article.
Tactile Temporal Discrimination Is Impaired in Myoclonus-Dystonia.
Tarrano C, Lamy JC, Delorme C, McGovern EM, Atkinson-Clement C, Brochard V, Thobois S, Tranchant C, Grabli D, Degos B, Corvol JC, Pedespan JM, Krystkoviak P, Houeto JL, Degardin A, Defebvre L, Apartis E, Vidailhet M, Roze E, Worbe Y. Tarrano C, et al. Among authors: pedespan jm. Mov Disord. 2020 Dec;35(12):2356-2357. doi: 10.1002/mds.28253. Epub 2020 Sep 22. Mov Disord. 2020. PMID: 32960985 No abstract available.
Absence epilepsies.
Loiseau P, Duché B, Pédespan JM. Loiseau P, et al. Among authors: pedespan jm. Epilepsia. 1995 Dec;36(12):1182-6. doi: 10.1111/j.1528-1157.1995.tb01060.x. Epilepsia. 1995. PMID: 7489694
[Obstructive hydrocephalus and Crouzon syndrome].
Levesque D, Coste V, Gimbert E, Duval MV, Pedespan JM, Lafourcade JP, Korobelnik JF. Levesque D, et al. Among authors: pedespan jm. J Fr Ophtalmol. 2019 Apr;42(4):e165-e168. doi: 10.1016/j.jfo.2018.08.012. Epub 2019 Mar 26. J Fr Ophtalmol. 2019. PMID: 30922627 French. No abstract available.
Visual sensory processing is altered in myoclonus dystonia.
Tarrano C, Wattiez N, Delorme C, McGovern EM, Brochard V, Thobois S, Tranchant C, Grabli D, Degos B, Corvol JC, Pedespan JM, Krystkoviak P, Houeto JL, Degardin A, Defebvre L, Valabrègue R, Vidailhet M, Pouget P, Roze E, Worbe Y. Tarrano C, et al. Among authors: pedespan jm. Mov Disord. 2020 Jan;35(1):151-160. doi: 10.1002/mds.27857. Epub 2019 Sep 30. Mov Disord. 2020. PMID: 31571302
Dissociation in reactive and proactive inhibitory control in Myoclonus dystonia.
Atkinson-Clement C, Tarrano C, Porte CA, Wattiez N, Delorme C, McGovern EM, Brochard V, Thobois S, Tranchant C, Grabli D, Degos B, Corvol JC, Pedespan JM, Krystkoviak P, Houeto JL, Degardin A, Defebvre L, Valabregue R, Rosso C, Apartis E, Vidailhet M, Pouget P, Roze E, Worbe Y. Atkinson-Clement C, et al. Among authors: pedespan jm. Sci Rep. 2020 Aug 18;10(1):13933. doi: 10.1038/s41598-020-70926-x. Sci Rep. 2020. PMID: 32811896 Free PMC article.
Callosotomy for intractable epilepsy: overall outcome.
Rougier A, Claverie B, Pedespan JM, Marchal C, Loiseau P. Rougier A, et al. Among authors: pedespan jm. J Neurosurg Sci. 1997 Mar;41(1):51-7. J Neurosurg Sci. 1997. PMID: 9273859 Review.
Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathy.
Vegas N, Cavallin M, Maillard C, Boddaert N, Toulouse J, Schaefer E, Lerman-Sagie T, Lev D, Magalie B, Moutton S, Haan E, Isidor B, Heron D, Milh M, Rondeau S, Michot C, Valence S, Wagner S, Hully M, Mignot C, Masurel A, Datta A, Odent S, Nizon M, Lazaro L, Vincent M, Cogné B, Guerrot AM, Arpin S, Pedespan JM, Caubel I, Pontier B, Troude B, Rivier F, Philippe C, Bienvenu T, Spitz MA, Bery A, Bahi-Buisson N. Vegas N, et al. Among authors: pedespan jm. Neurol Genet. 2018 Nov 7;4(6):e281. doi: 10.1212/NXG.0000000000000281. eCollection 2018 Dec. Neurol Genet. 2018. PMID: 30533527 Free PMC article.
99 results