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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 5
2008 6
2009 5
2010 6
2011 5
2012 6
2013 4
2014 3
2015 5
2016 4
2017 2
2018 3
2019 1
2020 1
2025 0

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170 results

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Page 1
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype.
Micol R, Ben Slama L, Suarez F, Le Mignot L, Beauté J, Mahlaoui N, Dubois d'Enghien C, Laugé A, Hall J, Couturier J, Vallée L, Delobel B, Rivier F, Nguyen K, Billette de Villemeur T, Stephan JL, Bordigoni P, Bertrand Y, Aladjidi N, Pedespan JM, Thomas C, Pellier I, Koenig M, Hermine O, Picard C, Moshous D, Neven B, Lanternier F, Blanche S, Tardieu M, Debré M, Fischer A, Stoppa-Lyonnet D; CEREDIH Network Investigators. Micol R, et al. J Allergy Clin Immunol. 2011 Aug;128(2):382-9.e1. doi: 10.1016/j.jaci.2011.03.052. Epub 2011 Jun 12. J Allergy Clin Immunol. 2011. PMID: 21665257
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.
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.
[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.
[Migraine in children].
Echenne B. Echenne B. Pediatrie. 1991;46(11):715-8. Pediatrie. 1991. PMID: 1661400 French. No abstract available.
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
[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.
170 results