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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
2024 0

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Search Results

113 results

Results by year

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Page 1
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, 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. 2008 Oct 14 [updated 2021 Jan 14]. 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: 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.
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.
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.
Genetic disorders affecting white matter in the pediatric age.
Di Rocco M, Biancheri R, Rossi A, Filocamo M, Tortori-Donati P. Di Rocco M, et al. Among authors: biancheri r. Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):85-93. doi: 10.1002/ajmg.b.30029. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15274047 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.
Periventricular nodular heterotopia in Smith-Magenis syndrome.
Capra V, Biancheri R, Morana G, Striano P, Novara F, Ferrero GB, Boeri L, Celle ME, Mancardi MM, Zuffardi O, Parrini E, Guerrini R. Capra V, et al. Among authors: biancheri r. Am J Med Genet A. 2014 Dec;164A(12):3142-7. doi: 10.1002/ajmg.a.36742. Epub 2014 Sep 24. Am J Med Genet A. 2014. PMID: 25257626
113 results