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

Year Number of Results
1986 1
1987 1
1988 1
1989 1
1992 1
1995 1
1996 1
1997 2
1998 4
1999 1
2001 2
2002 2
2003 2
2004 7
2005 5
2006 5
2007 6
2008 4
2009 2
2010 4
2011 3
2012 6
2013 4
2014 6
2015 12
2016 7
2017 8
2018 8
2019 7
2020 4
2021 5
2022 3
2023 1
2024 0

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106 results

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Page 1
Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis.
D'Antonio F, Pagani G, Familiari A, Khalil A, Sagies TL, Malinger G, Leibovitz Z, Garel C, Moutard ML, Pilu G, Bhide A, Acharya G, Leombroni M, Manzoli L, Papageorghiou A, Prefumo F. D'Antonio F, et al. Among authors: moutard ml. Pediatrics. 2016 Sep;138(3):e20160445. doi: 10.1542/peds.2016-0445. Pediatrics. 2016. PMID: 27581855 Review.
Biometry of the corpus callosum in children: MR imaging reference data.
Garel C, Cont I, Alberti C, Josserand E, Moutard ML, Ducou le Pointe H. Garel C, et al. Among authors: moutard ml. AJNR Am J Neuroradiol. 2011 Sep;32(8):1436-43. doi: 10.3174/ajnr.A2542. Epub 2011 Jul 28. AJNR Am J Neuroradiol. 2011. PMID: 21799035 Free PMC article.
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.
Crow YJ, Chase DS, Lowenstein Schmidt J, Szynkiewicz M, Forte GM, Gornall HL, Oojageer A, Anderson B, Pizzino A, Helman G, Abdel-Hamid MS, Abdel-Salam GM, Ackroyd S, Aeby A, Agosta G, Albin C, Allon-Shalev S, Arellano M, Ariaudo G, Aswani V, Babul-Hirji R, Baildam EM, Bahi-Buisson N, Bailey KM, Barnerias C, Barth M, Battini R, Beresford MW, Bernard G, Bianchi M, Billette de Villemeur T, Blair EM, Bloom M, Burlina AB, Carpanelli ML, Carvalho DR, Castro-Gago M, Cavallini A, Cereda C, Chandler KE, Chitayat DA, Collins AE, Sierra Corcoles C, Cordeiro NJ, Crichiutti G, Dabydeen L, Dale RC, D'Arrigo S, De Goede CG, De Laet C, De Waele LM, Denzler I, Desguerre I, Devriendt K, Di Rocco M, Fahey MC, Fazzi E, Ferrie CD, Figueiredo A, Gener B, Goizet C, Gowrinathan NR, Gowrishankar K, Hanrahan D, Isidor B, Kara B, Khan N, King MD, Kirk EP, Kumar R, Lagae L, Landrieu P, Lauffer H, Laugel V, La Piana R, Lim MJ, Lin JP, Linnankivi T, Mackay MT, Marom DR, Marques Lourenço C, McKee SA, Moroni I, Morton JE, Moutard ML, Murray K, Nabbout R, Nampoothiri S, Nunez-Enamorado N, Oades PJ, Olivieri I, Ostergaard JR, Pérez-Dueñas B, Prendiville JS, Ramesh V, Rasmussen M, Régal L, Ricci F, Rio M, Ro… See abstract for full author list ➔ Crow YJ, et al. Among authors: moutard ml. Am J Med Genet A. 2015 Feb;167A(2):296-312. doi: 10.1002/ajmg.a.36887. Epub 2015 Jan 16. Am J Med Genet A. 2015. PMID: 25604658 Free PMC article.
Developmental aspects of normal EEG.
Plouin P, Kaminska A, Moutard ML, Soufflet C. Plouin P, et al. Among authors: moutard ml. Handb Clin Neurol. 2013;111:79-85. doi: 10.1016/B978-0-444-52891-9.00007-5. Handb Clin Neurol. 2013. PMID: 23622152 Review.
Tremor-like subcortical myoclonus in STXBP1 encephalopathy.
Loussouarn A, Doummar D, Beaugendre Y, Bienvenu T, Charles P, Depienne C, Dorison N, Heide S, Héron D, Ioos C, Keren B, Métreau J, Mochel F, Moutard ML, Ravelli C, Apartis E, Mignot C. Loussouarn A, et al. Among authors: moutard ml. Eur J Paediatr Neurol. 2021 Sep;34:62-66. doi: 10.1016/j.ejpn.2021.06.005. Epub 2021 Jul 3. Eur J Paediatr Neurol. 2021. PMID: 34392114
[Indications of electroencephalogram in the newborn].
Lamblin MD, André M, Auzoux M, Bednarek N, Bour F, Charollais A, Cheliout-Heraut F, D'Allest AM, De Bellecize J, Delanoe C, Furby A, Frenkel AL, Keo-Kosal P, Mony L, Moutard ML, Navelet Y, Nedelcoux H, Nguyen TT, Nogues B, Plouin P, Salefranque F, Soufflet C, Touzery de Villepin A, Vecchierini MF, Wallois F, Esquivel-Walls E. Lamblin MD, et al. Among authors: moutard ml. Arch Pediatr. 2004 Jul;11(7):829-33. doi: 10.1016/j.arcped.2004.01.031. Arch Pediatr. 2004. PMID: 15234381 Review. French.
MRI of the fetal posterior fossa.
Adamsbaum C, Moutard ML, André C, Merzoug V, Ferey S, Quéré MP, Lewin F, Fallet-Bianco C. Adamsbaum C, et al. Among authors: moutard ml. Pediatr Radiol. 2005 Feb;35(2):124-40. doi: 10.1007/s00247-004-1316-3. Epub 2004 Nov 23. Pediatr Radiol. 2005. PMID: 15565345 Review.
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.
Marsh APL, Edwards TJ, Galea C, Cooper HM, Engle EC, Jamuar SS, Méneret A, Moutard ML, Nava C, Rastetter A, Robinson G, Rouleau G, Roze E, Spencer-Smith M, Trouillard O, Billette de Villemeur T, Walsh CA, Yu TW; IRC5 Consortium; Heron D, Sherr EH, Richards LJ, Depienne C, Leventer RJ, Lockhart PJ. Marsh APL, et al. Among authors: moutard ml. Hum Mutat. 2018 Jan;39(1):23-39. doi: 10.1002/humu.23361. Epub 2017 Nov 11. Hum Mutat. 2018. PMID: 29068161 Free PMC article. Review.
Prenatal diagnosis of vermian cyst: a new type of posterior fossa cyst.
Chanclud J, Valence S, Perre SV, Guilbaud L, Moutard ML, Jouannic JM, Ducou Le Pointe H, Blondiaux E, Garel C. Chanclud J, et al. Among authors: moutard ml. Pediatr Radiol. 2023 Mar;53(3):461-469. doi: 10.1007/s00247-022-05531-3. Epub 2022 Oct 24. Pediatr Radiol. 2023. PMID: 36274068
106 results