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

Year Number of Results
1981 1
1983 1
1984 2
1985 1
1988 3
1989 2
1990 2
1991 2
1992 5
1993 8
1994 8
1995 10
1996 9
1997 9
1998 14
1999 6
2000 7
2001 3
2002 4
2003 3
2004 5
2005 4
2006 3
2007 3
2008 7
2009 4
2010 2
2012 4
2013 5
2014 6
2015 5
2016 5
2018 1
2024 0

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147 results

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Page 1
Bilateral frontoparietal polymicrogyria.
Jain P, Sharma S, Bahi-Buisson N, Beldjord C, Aneja S. Jain P, et al. Among authors: beldjord c. Indian J Pediatr. 2015 Apr;82(4):390-1. doi: 10.1007/s12098-014-1614-1. Epub 2014 Nov 23. Indian J Pediatr. 2015. PMID: 25416088 No abstract available.
From adhalinopathies to alpha-sarcoglycanopathies: an overview.
Jeanpierre M, Carrié A, Piccolo F, Leturcq F, Azibi K, De Toma C, Beldjord C, Merlini L, Voit T, Romero N, Sunada Y, Tomé FM, Fardeau M, Campbell KP, Kaplan JC. Jeanpierre M, et al. Among authors: beldjord c. Neuromuscul Disord. 1996 Dec;6(6):463-5. doi: 10.1016/s0960-8966(96)00394-x. Neuromuscul Disord. 1996. PMID: 9027856 Review. No abstract available.
Human disorders of cortical development: from past to present.
Francis F, Meyer G, Fallet-Bianco C, Moreno S, Kappeler C, Socorro AC, Tuy FP, Beldjord C, Chelly J. Francis F, et al. Among authors: beldjord c. Eur J Neurosci. 2006 Feb;23(4):877-93. doi: 10.1111/j.1460-9568.2006.04649.x. Eur J Neurosci. 2006. PMID: 16519653 Review.
Dental caries and enamelin haplotype.
Chaussain C, Bouazza N, Gasse B, Laffont AG, Opsahl Vital S, Davit-Béal T, Moulis E, Chabadel O, Hennequin M, Courson F, Droz D, Vaysse F, Laboux O, Tassery H, Carel JC, Alcais A, Treluyer JM, Beldjord C, Sire JY. Chaussain C, et al. Among authors: beldjord c. J Dent Res. 2014 Apr;93(4):360-5. doi: 10.1177/0022034514522060. Epub 2014 Jan 31. J Dent Res. 2014. PMID: 24487377
Beta-thalassemia in Algeria.
Labie D, Bennani C, Beldjord C. Labie D, et al. Among authors: beldjord c. Ann N Y Acad Sci. 1990;612:43-54. doi: 10.1111/j.1749-6632.1990.tb24289.x. Ann N Y Acad Sci. 1990. PMID: 1705410 No abstract available.
X-chromosome inactivation in female patients with Fabry disease.
Echevarria L, Benistan K, Toussaint A, Dubourg O, Hagege AA, Eladari D, Jabbour F, Beldjord C, De Mazancourt P, Germain DP. Echevarria L, et al. Among authors: beldjord c. Clin Genet. 2016 Jan;89(1):44-54. doi: 10.1111/cge.12613. Epub 2015 Jun 22. Clin Genet. 2016. PMID: 25974833
The wide spectrum of tubulinopathies: what are the key features for the diagnosis?
Bahi-Buisson N, Poirier K, Fourniol F, Saillour Y, Valence S, Lebrun N, Hully M, Bianco CF, Boddaert N, Elie C, Lascelles K, Souville I; LIS-Tubulinopathies Consortium; Beldjord C, Chelly J. Bahi-Buisson N, et al. Among authors: beldjord c. Brain. 2014 Jun;137(Pt 6):1676-700. doi: 10.1093/brain/awu082. Brain. 2014. PMID: 24860126
Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.
Zillhardt JL, Poirier K, Broix L, Lebrun N, Elmorjani A, Martinovic J, Saillour Y, Muraca G, Nectoux J, Bessieres B, Fallet-Bianco C, Lyonnet S, Dulac O, Odent S, Rejeb I, Ben Jemaa L, Rivier F, Pinson L, Geneviève D, Musizzano Y, Bigi N, Leboucq N, Giuliano F, Philip N, Vilain C, Van Bogaert P, Maurey H, Beldjord C, Artiguenave F, Boland A, Olaso R, Masson C, Nitschké P, Deleuze JF, Bahi-Buisson N, Chelly J. Zillhardt JL, et al. Among authors: beldjord c. Eur J Hum Genet. 2016 Apr;24(4):611-4. doi: 10.1038/ejhg.2015.192. Epub 2015 Sep 23. Eur J Hum Genet. 2016. PMID: 26395554 Free PMC article.
Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria.
Poirier K, Saillour Y, Fourniol F, Francis F, Souville I, Valence S, Desguerre I, Marie Lepage J, Boddaert N, Line Jacquemont M, Beldjord C, Chelly J, Bahi-Buisson N. Poirier K, et al. Among authors: beldjord c. Eur J Hum Genet. 2013 Apr;21(4):381-5. doi: 10.1038/ejhg.2012.195. Epub 2012 Sep 5. Eur J Hum Genet. 2013. PMID: 22948023 Free PMC article.
147 results