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

Year Number of Results
1989 1
1990 2
1993 3
1994 1
1995 1
1997 3
1998 3
1999 1
2000 3
2001 3
2002 5
2003 4
2004 1
2005 2
2006 2
2007 4
2008 1
2009 4
2010 10
2011 9
2012 7
2013 7
2014 6
2015 11
2016 13
2017 9
2018 10
2019 6
2020 1
2024 0

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122 results

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Page 1
Cone rod dystrophies.
Hamel CP. Hamel CP. Orphanet J Rare Dis. 2007 Feb 1;2:7. doi: 10.1186/1750-1172-2-7. Orphanet J Rare Dis. 2007. PMID: 17270046 Free PMC article. Review.
Optic Atrophy Type 1.
Delettre-Cribaillet C, Hamel CP, Lenaers G. Delettre-Cribaillet C, et al. Among authors: hamel cp. 2007 Jul 13 [updated 2015 Nov 12]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2007 Jul 13 [updated 2015 Nov 12]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301426 Free Books & Documents. Review.
How can we prevent myopia progression?
Chassine T, Villain M, Hamel CP, Daien V. Chassine T, et al. Among authors: hamel cp. Eur J Ophthalmol. 2015 Jul-Aug;25(4):280-5. doi: 10.5301/ejo.5000571. Epub 2015 Feb 3. Eur J Ophthalmol. 2015. PMID: 25655598 Review.
Choroideremia: towards a therapy.
Kalatzis V, Hamel CP, MacDonald IM; First International Choroideremia Research Symposium. Kalatzis V, et al. Among authors: hamel cp. Am J Ophthalmol. 2013 Sep;156(3):433-437.e3. doi: 10.1016/j.ajo.2013.05.009. Epub 2013 Jun 28. Am J Ophthalmol. 2013. PMID: 23810476
The retinal pigment epithelium in health and disease.
Sparrow JR, Hicks D, Hamel CP. Sparrow JR, et al. Among authors: hamel cp. Curr Mol Med. 2010 Dec;10(9):802-23. doi: 10.2174/156652410793937813. Curr Mol Med. 2010. PMID: 21091424 Free PMC article. Review.
Clinical Evaluation and Cone Alterations in Choroideremia.
Nabholz N, Lorenzini MC, Bocquet B, Lacroux A, Faugère V, Roux AF, Kalatzis V, Meunier I, Hamel CP. Nabholz N, et al. Among authors: hamel cp. Ophthalmology. 2016 Aug;123(8):1830-1832. doi: 10.1016/j.ophtha.2016.02.025. Epub 2016 Mar 15. Ophthalmology. 2016. PMID: 26992839 No abstract available.
Reply: The expanding neurological phenotype of DNM1L-related disorders.
Gerber S, Charif M, Chevrollier A, Chaumette T, Angebault C, Kane S, Paris A, Alban J, Quiles M, Delettre C, Bonneau D, Procaccio V, Amati-Bonneau P, Reynier P, Leruez S, Calmon R, Boddaert N, Funalot B, Rio M, Bouccara D, Meunier I, Sesaki H, Kaplan J, Hamel CP, Rozet JM, Lenaers G. Gerber S, et al. Among authors: hamel cp. Brain. 2018 Apr 1;141(4):e29. doi: 10.1093/brain/awy027. Brain. 2018. PMID: 29529130 No abstract available.
Genotyping microarray for CSNB-associated genes.
Zeitz C, Labs S, Lorenz B, Forster U, Uksti J, Kroes HY, De Baere E, Leroy BP, Cremers FP, Wittmer M, van Genderen MM, Sahel JA, Audo I, Poloschek CM, Mohand-Saïd S, Fleischhauer JC, Hüffmeier U, Moskova-Doumanova V, Levin AV, Hamel CP, Leifert D, Munier FL, Schorderet DF, Zrenner E, Friedburg C, Wissinger B, Kohl S, Berger W. Zeitz C, et al. Among authors: hamel cp. Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5919-26. doi: 10.1167/iovs.09-3548. Epub 2009 Jul 2. Invest Ophthalmol Vis Sci. 2009. PMID: 19578023 Free article.
Mutations in IMPG1 cause vitelliform macular dystrophies.
Manes G, Meunier I, Avila-Fernández A, Banfi S, Le Meur G, Zanlonghi X, Corton M, Simonelli F, Brabet P, Labesse G, Audo I, Mohand-Said S, Zeitz C, Sahel JA, Weber M, Dollfus H, Dhaenens CM, Allorge D, De Baere E, Koenekoop RK, Kohl S, Cremers FP, Hollyfield JG, Sénéchal A, Hebrard M, Bocquet B, Ayuso García C, Hamel CP. Manes G, et al. Among authors: hamel cp. Am J Hum Genet. 2013 Sep 5;93(3):571-8. doi: 10.1016/j.ajhg.2013.07.018. Epub 2013 Aug 29. Am J Hum Genet. 2013. PMID: 23993198 Free PMC article.
122 results