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Pathogenic variants in KCNQ2 cause intellectual deficiency without epilepsy: Broadening the phenotypic spectrum of a potassium channelopathy.
Am J Med Genet A. 2021 Jun;185(6):1803-1815. doi: 10.1002/ajmg.a.62181. Epub 2021 Mar 23.
Am J Med Genet A. 2021.
PMID: 33754465
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.
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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
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Prenatal unilateral cerebellar hypoplasia in a series of 26 cases: significance and implications for prenatal diagnosis.
Massoud M, Cagneaux M, Garel C, Varene N, Moutard ML, Billette T, Benezit A, Rougeot C, Jouannic JM, Massardier J, Gaucherand P, Desportes V, Guibaud L.
Massoud M, et al. Among authors: billette t.
Ultrasound Obstet Gynecol. 2014 Oct;44(4):447-54. doi: 10.1002/uog.13217.
Ultrasound Obstet Gynecol. 2014.
PMID: 24185815
Free article.
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[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.
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