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Year Number of Results
2009 1
2014 1
2016 1
2020 1
2021 1
2022 0
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Page 1
Movement disorders in patients with alternating hemiplegia: "Soft" and "stiff" at the same time.
Panagiotakaki E, Doummar D, Nogue E, Nagot N, Lesca G, Riant F, Nicole S, Delaygue C, Barthez MA, Nassogne MC, Dusser A, Vallée L, Billette T, Bourgeois M, Ioos C, Gitiaux C, Laroche C, Milh M, Portes VD, Arzimanoglou A, Roubertie A; AHC–Movement Disorder Study Group. Panagiotakaki E, et al. Among authors: billette t. Neurology. 2020 Mar 31;94(13):e1378-e1385. doi: 10.1212/WNL.0000000000009175. Epub 2020 Mar 2. Neurology. 2020. PMID: 32123049
ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability.
Mignot C, Moutard ML, Rastetter A, Boutaud L, Heide S, Billette T, Doummar D, Garel C, Afenjar A, Jacquette A, Lacombe D, Verloes A, Bole-Feysot C, Nitschké P, Masson C, Faudet A, Lesne F, Bienvenu T, Alby C, Attié-Bitach T, Depienne C, Nava C, Héron D. Mignot C, et al. Among authors: billette t. Brain. 2016 Nov 1;139(11):e64. doi: 10.1093/brain/aww181. Brain. 2016. PMID: 27474218 No abstract available.
[Inaugural trunk dystonia revealing Langerhans cell histiocytosis].
Georget-Bouquinet E, Madhi F, Delacourt C, Billette T, Debray D, Reinert P, Donadieu J. Georget-Bouquinet E, et al. Among authors: billette t. Arch Pediatr. 2009 Jul;16(7):1021-3. doi: 10.1016/j.arcped.2009.03.011. Epub 2009 May 9. Arch Pediatr. 2009. PMID: 19428224 French.