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

Year Number of Results
1991 1
1992 1
1993 1
1995 1
1996 1
1998 2
1999 1
2000 2
2001 2
2002 1
2003 4
2005 1
2006 1
2007 3
2008 4
2009 3
2010 7
2011 3
2012 1
2013 4
2014 8
2015 5
2016 3
2018 1
2019 2
2020 4
2021 2
2024 0

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61 results

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Page 1
Dentin biomodification: strategies, renewable resources and clinical applications.
Bedran-Russo AK, Pauli GF, Chen SN, McAlpine J, Castellan CS, Phansalkar RS, Aguiar TR, Vidal CM, Napotilano JG, Nam JW, Leme AA. Bedran-Russo AK, et al. Among authors: castellan cs. Dent Mater. 2014 Jan;30(1):62-76. doi: 10.1016/j.dental.2013.10.012. Epub 2013 Dec 3. Dent Mater. 2014. PMID: 24309436 Free PMC article. Review.
Experimental designs for small randomised clinical trials: an algorithm for choice.
Cornu C, Kassai B, Fisch R, Chiron C, Alberti C, Guerrini R, Rosati A, Pons G, Tiddens H, Chabaud S, Caudri D, Ballot C, Kurbatova P, Castellan AC, Bajard A, Nony P; CRESim & Epi-CRESim Project Groups; Aarons L, Bajard A, Ballot C, Bertrand Y, Bretz F, Caudri D, Castellan C, Chabaud S, Cornu C, Dufour F, Dunger-Baldauf C, Dupont JM, Fisch R, Guerrini R, Jullien V, Kassaï B, Nony P, Ogungbenro K, Pérol D, Pons G, Tiddens H, Rosati A, Alberti C, Chiron C, Kurbatova P, Nabbout R. Cornu C, et al. Among authors: castellan c. Orphanet J Rare Dis. 2013 Mar 25;8:48. doi: 10.1186/1750-1172-8-48. Orphanet J Rare Dis. 2013. PMID: 23531234 Free PMC article. Review.
Trisomy 2p: analysis of unusual phenotypic findings.
Lurie IW, Ilyina HG, Gurevich DB, Rumyantseva NV, Naumchik IV, Castellan C, Hoeller A, Schinzel A. Lurie IW, et al. Among authors: castellan c. Am J Med Genet. 1995 Jan 16;55(2):229-36. doi: 10.1002/ajmg.1320550216. Am J Med Genet. 1995. PMID: 7717424 Review.
Model of mucociliary clearance in cystic fibrosis lungs.
Kurbatova P, Bessonov N, Volpert V, Tiddens HA, Cornu C, Nony P, Caudri D; CRESim Working Group. Kurbatova P, et al. J Theor Biol. 2015 May 7;372:81-8. doi: 10.1016/j.jtbi.2015.02.023. Epub 2015 Mar 5. J Theor Biol. 2015. PMID: 25746843
A methodological framework for drug development in rare diseases.
Nony P, Kurbatova P, Bajard A, Malik S, Castellan C, Chabaud S, Volpert V, Eymard N, Kassai B, Cornu C; CRESim; Epi-CRESim. Nony P, et al. Among authors: castellan c. Orphanet J Rare Dis. 2014 Nov 18;9:164. doi: 10.1186/s13023-014-0164-y. Orphanet J Rare Dis. 2014. PMID: 25774598 Free PMC article.
Single-nucleotide polymorphism array-based characterization of ring chromosome 18.
Spreiz A, Guilherme RS, Castellan C, Green A, Rittinger O, Wellek B, Utermann B, Erdel M, Fauth C, Haberlandt E, Kim CA, Kulikowski LD, Meloni VA, Utermann G, Zschocke J, Melaragno MI, Kotzot D. Spreiz A, et al. Among authors: castellan c. J Pediatr. 2013 Oct;163(4):1174-8.e3. doi: 10.1016/j.jpeds.2013.06.005. Epub 2013 Jul 19. J Pediatr. 2013. PMID: 23876976
CNGA3 mutations in hereditary cone photoreceptor disorders.
Wissinger B, Gamer D, Jägle H, Giorda R, Marx T, Mayer S, Tippmann S, Broghammer M, Jurklies B, Rosenberg T, Jacobson SG, Sener EC, Tatlipinar S, Hoyng CB, Castellan C, Bitoun P, Andreasson S, Rudolph G, Kellner U, Lorenz B, Wolff G, Verellen-Dumoulin C, Schwartz M, Cremers FP, Apfelstedt-Sylla E, Zrenner E, Salati R, Sharpe LT, Kohl S. Wissinger B, et al. Among authors: castellan c. Am J Hum Genet. 2001 Oct;69(4):722-37. doi: 10.1086/323613. Epub 2001 Aug 30. Am J Hum Genet. 2001. PMID: 11536077 Free PMC article.
61 results