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Results by year

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
2024 0

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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.
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.
[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.
[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.
[The varied etiologies of childhood-onset dystonia].
Roubertie A, Rivier F, Humbertclaude V, Tuffery S, Cavalier L, Cheminal R, Coubes P, Echenne B. Roubertie A, et al. Among authors: echenne b. Rev Neurol (Paris). 2002 Apr;158(4):413-24. Rev Neurol (Paris). 2002. PMID: 11984483 Review. French.
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.
Early hemispherectomy in a case of hemimegalencephaly.
Humbertclaude VT, Coubes PA, Robain O, Echenne BB. Humbertclaude VT, et al. Among authors: echenne bb. Pediatr Neurosurg. 1997 Nov;27(5):268-71. doi: 10.1159/000121265. Pediatr Neurosurg. 1997. PMID: 9620005 Review.
Hemimegalencephaly and neurofibromatosis.
Cusmai R, Curatolo P, Mangano S, Cheminal R, Echenne B. Cusmai R, et al. Among authors: echenne b. Neuropediatrics. 1990 Nov;21(4):179-82. doi: 10.1055/s-2008-1071490. Neuropediatrics. 1990. PMID: 2127080
166 results