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

Year Number of Results
1975 1
1976 3
1977 1
1978 2
1980 2
1981 4
1982 2
1983 5
1984 6
1985 3
1986 4
1987 2
1988 5
1989 3
1990 1
1991 4
1992 8
1993 2
1994 3
1995 1
1996 5
1997 7
1998 6
1999 5
2000 7
2001 8
2002 6
2003 5
2004 7
2005 6
2006 6
2007 4
2008 5
2009 4
2010 6
2011 4
2012 6
2013 4
2014 3
2015 5
2016 4
2017 2
2018 2
2019 1
2020 1
2022 0
Text availability
Article attribute
Article type
Publication date

Search Results

166 results
Results by year
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Page 1
Insights in Developmental Coordination Disorder.
Farmer M, Echenne B, Drouin R, Bentourkia M. Farmer M, et al. Among authors: echenne b. Curr Pediatr Rev. 2017;13(2):111-119. doi: 10.2174/1573396313666170726113550. Curr Pediatr Rev. 2017. PMID: 28745216 Review.
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.
Hu H, Haas SA, Chelly J, Van Esch H, Raynaud M, de Brouwer AP, Weinert S, Froyen G, Frints SG, Laumonnier F, Zemojtel T, Love MI, Richard H, Emde AK, Bienek M, Jensen C, Hambrock M, Fischer U, Langnick C, Feldkamp M, Wissink-Lindhout W, Lebrun N, Castelnau L, Rucci J, Montjean R, Dorseuil O, Billuart P, Stuhlmann T, Shaw M, Corbett MA, Gardner A, Willis-Owen S, Tan C, Friend KL, Belet S, van Roozendaal KE, Jimenez-Pocquet M, Moizard MP, Ronce N, Sun R, O'Keeffe S, Chenna R, van Bömmel A, Göke J, Hackett A, Field M, Christie L, Boyle J, Haan E, Nelson J, Turner G, Baynam G, Gillessen-Kaesbach G, Müller U, Steinberger D, Budny B, Badura-Stronka M, Latos-Bieleńska A, Ousager LB, Wieacker P, Rodríguez Criado G, Bondeson ML, Annerén G, Dufke A, Cohen M, Van Maldergem L, Vincent-Delorme C, Echenne B, Simon-Bouy B, Kleefstra T, Willemsen M, Fryns JP, Devriendt K, Ullmann R, Vingron M, Wrogemann K, Wienker TF, Tzschach A, van Bokhoven H, Gecz J, Jentsch TJ, Chen W, Ropers HH, Kalscheuer VM. Hu H, et al. Among authors: echenne b. Mol Psychiatry. 2016 Jan;21(1):133-48. doi: 10.1038/mp.2014.193. Epub 2015 Feb 3. Mol Psychiatry. 2016. PMID: 25644381 Free PMC article.
[Treatment of childhood dystonia].
Roubertie A, Roze E, Bahi-Buisson N, Payet C, Echenne B, Doummar D. Roubertie A, et al. Among authors: echenne b. Arch Pediatr. 2010 May;17(5):540-53. doi: 10.1016/j.arcped.2010.02.016. Epub 2010 Apr 1. Arch Pediatr. 2010. PMID: 20362421 Review. French.
Congenital and infantile myotonic dystrophy.
Echenne B, Bassez G. Echenne B, et al. Handb Clin Neurol. 2013;113:1387-93. doi: 10.1016/B978-0-444-59565-2.00009-5. Handb Clin Neurol. 2013. PMID: 23622362 Review.
Cognitive impairment in children with CACNA1A mutations.
Humbertclaude V, Riant F, Krams B, Zimmermann V, Nagot N, Annequin D, Echenne B, Tournier-Lasserve E, Roubertie A; Episodic Syndrome Consortium. Humbertclaude V, et al. Among authors: echenne b. Dev Med Child Neurol. 2020 Mar;62(3):330-337. doi: 10.1111/dmcn.14261. Epub 2019 May 21. Dev Med Child Neurol. 2020. PMID: 31115040 Free article.
[Acute motor deficit in childhood: diagnosis management].
Roubertie A, Soëte S, Meyer P, Echenne B, Rivier F, Langlois C. Roubertie A, et al. Among authors: echenne b. Arch Pediatr. 2010 Mar;17(3):325-32. doi: 10.1016/j.arcped.2009.11.017. Epub 2009 Dec 31. Arch Pediatr. 2010. PMID: 20045298 Review. French.
[Movement disorders in childhood: therapeutic update].
Roubertie A, Leydet J, Rivier F, Humbertclaude V, Cheminal R, Echenne B. Roubertie A, et al. Among authors: echenne b. Arch Pediatr. 2004 Aug;11(8):951-4. doi: 10.1016/j.arcped.2004.01.009. Arch Pediatr. 2004. PMID: 15288089 Review. French.
166 results