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Results by year

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

Year Number of Results
1993 2
1997 1
1998 2
1999 2
2000 2
2001 8
2002 3
2003 2
2004 8
2005 4
2006 8
2007 10
2008 8
2009 9
2010 8
2011 8
2012 13
2013 11
2014 12
2015 7
2016 3
2017 2
2020 1
2021 1
2022 0
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Search Results

113 results
Results by year
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Page 1
Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
Rice G, Patrick T, Parmar R, Taylor CF, Aeby A, Aicardi J, Artuch R, Montalto SA, Bacino CA, Barroso B, Baxter P, Benko WS, Bergmann C, Bertini E, Biancheri R, Blair EM, Blau N, Bonthron DT, Briggs T, Brueton LA, Brunner HG, Burke CJ, Carr IM, Carvalho DR, Chandler KE, Christen HJ, Corry PC, Cowan FM, Cox H, D'Arrigo S, Dean J, De Laet C, De Praeter C, Dery C, Ferrie CD, Flintoff K, Frints SG, Garcia-Cazorla A, Gener B, Goizet C, Goutieres F, Green AJ, Guet A, Hamel BC, Hayward BE, Heiberg A, Hennekam RC, Husson M, Jackson AP, Jayatunga R, Jiang YH, Kant SG, Kao A, King MD, Kingston HM, Klepper J, van der Knaap MS, Kornberg AJ, Kotzot D, Kratzer W, Lacombe D, Lagae L, Landrieu PG, Lanzi G, Leitch A, Lim MJ, Livingston JH, Lourenco CM, Lyall EG, Lynch SA, Lyons MJ, Marom D, McClure JP, McWilliam R, Melancon SB, Mewasingh LD, Moutard ML, Nischal KK, Ostergaard JR, Prendiville J, Rasmussen M, Rogers RC, Roland D, Rosser EM, Rostasy K, Roubertie A, Sanchis A, Schiffmann R, Scholl-Burgi S, Seal S, Shalev SA, Corcoles CS, Sinha GP, Soler D, Spiegel R, Stephenson JB, Tacke U, Tan TY, Till M, Tolmie JL, Tomlin P, Vagnarelli F, Valente EM, Van Coster RN, Van der Aa N, Vanderver A, Vles JS, Voit T, Wassmer E, Weschke B, Whiteford ML, Willemsen MA, Zankl A, Zuberi SM, Orcesi S, Fazzi E, Lebon P, Crow YJ. Rice G, et al. Among authors: biancheri r. Am J Hum Genet. 2007 Oct;81(4):713-25. doi: 10.1086/521373. Epub 2007 Sep 4. Am J Hum Genet. 2007. PMID: 17846997 Free PMC article.
Hypomyelination and Congenital Cataract.
Wolf NI, Biancheri R, Zara F, Bruno C, Gazzerro E, Rossi A, van der Knaap MS, Minetti C. Wolf NI, et al. Among authors: biancheri r. 2008 Oct 14 [updated 2021 Jan 14]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2008 Oct 14 [updated 2021 Jan 14]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301737 Free Books & Documents. Review.
Magnetic resonance spectroscopy in metabolic disorders.
Rossi A, Biancheri R. Rossi A, et al. Among authors: biancheri r. Neuroimaging Clin N Am. 2013 Aug;23(3):425-48. doi: 10.1016/j.nic.2012.12.013. Epub 2013 Feb 10. Neuroimaging Clin N Am. 2013. PMID: 23928198 Review.
Spinal dysraphism: MR imaging rationale.
Rossi A, Cama A, Piatelli G, Ravegnani M, Biancheri R, Tortori-Donati P. Rossi A, et al. Among authors: biancheri r. J Neuroradiol. 2004 Jan;31(1):3-24. doi: 10.1016/s0150-9861(04)96875-7. J Neuroradiol. 2004. PMID: 15026728 Review.
Muscle and the cerebellum.
Biancheri R, Rossi A, Bruno C, Minetti C. Biancheri R, et al. Neuroradiol J. 2007 Aug 31;20(4):427-33. doi: 10.1177/197140090702000407. Epub 2007 Aug 31. Neuroradiol J. 2007. PMID: 24299703 No abstract available.
AIMP1/p43 mutation and PMLD.
Biancheri R, Rossi A, Zara F, Filocamo M. Biancheri R, et al. Am J Hum Genet. 2011 Mar 11;88(3):391; author reply 393-5. doi: 10.1016/j.ajhg.2011.02.003. Am J Hum Genet. 2011. PMID: 21397066 Free PMC article. No abstract available.
Magnetic resonance imaging of spinal dysraphism.
Tortori-Donati P, Rossi A, Biancheri R, Cama A. Tortori-Donati P, et al. Among authors: biancheri r. Top Magn Reson Imaging. 2001 Dec;12(6):375-409. doi: 10.1097/00002142-200112000-00003. Top Magn Reson Imaging. 2001. PMID: 11744877 Review.
Imaging in spine and spinal cord malformations.
Rossi A, Biancheri R, Cama A, Piatelli G, Ravegnani M, Tortori-Donati P. Rossi A, et al. Among authors: biancheri r. Eur J Radiol. 2004 May;50(2):177-200. doi: 10.1016/j.ejrad.2003.10.015. Eur J Radiol. 2004. PMID: 15081131 Review.
Hypomyelination and congenital cataract: broadening the clinical phenotype.
Biancheri R, Zara F, Rossi A, Mathot M, Nassogne MC, Yalcinkaya C, Erturk O, Tuysuz B, Di Rocco M, Gazzerro E, Bugiani M, van Spaendonk R, Sistermans EA, Minetti C, van der Knaap MS, Wolf NI. Biancheri R, et al. Arch Neurol. 2011 Sep;68(9):1191-4. doi: 10.1001/archneurol.2011.201. Arch Neurol. 2011. PMID: 21911699 Review.
113 results