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

Year Number of Results
2003 5
2004 2
2005 2
2006 1
2007 3
2008 2
2009 2
2010 1
2011 2
2012 2
2014 1
2015 3
2016 2
2017 1
2024 0

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26 results

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Page 1
Von hippel-lindau disease and erythrocytosis.
Capodimonti S, Teofili L, Martini M, Cenci T, Iachininoto MG, Nuzzolo ER, Bianchi M, Murdolo M, Leone G, Larocca LM. Capodimonti S, et al. Among authors: murdolo m. J Clin Oncol. 2012 May 1;30(13):e137-9. doi: 10.1200/JCO.2011.38.6797. Epub 2012 Mar 5. J Clin Oncol. 2012. PMID: 22393103 No abstract available.
Trisomy 12p and monosomy 4p: phenotype-genotype correlation.
Benussi DG, Costa P, Zollino M, Murdolo M, Petix V, Carrozzi M, Pecile V. Benussi DG, et al. Among authors: murdolo m. Genet Test Mol Biomarkers. 2009 Apr;13(2):199-204. doi: 10.1089/gtmb.2008.0109. Genet Test Mol Biomarkers. 2009. PMID: 19378504
Wolf-Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter.
Iwanowski PS, Panasiuk B, Van Buggenhout G, Murdolo M, Myśliwiec M, Maas NM, Lattante S, Korniszewski L, Posmyk R, Pilch J, Zajączek S, Fryns JP, Zollino M, Midro AT. Iwanowski PS, et al. Among authors: murdolo m. Am J Med Genet A. 2011 Aug;155A(8):1833-47. doi: 10.1002/ajmg.a.34005. Epub 2011 Jul 8. Am J Med Genet A. 2011. PMID: 21744486
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria.
Marangi G, Ricciardi S, Orteschi D, Lattante S, Murdolo M, Dallapiccola B, Biscione C, Lecce R, Chiurazzi P, Romano C, Greco D, Pettinato R, Sorge G, Pantaleoni C, Alfei E, Toldo I, Magnani C, Bonanni P, Martinez F, Serra G, Battaglia D, Lettori D, Vasco G, Baroncini A, Daolio C, Zollino M. Marangi G, et al. Among authors: murdolo m. Am J Med Genet A. 2011 Jul;155A(7):1536-45. doi: 10.1002/ajmg.a.34070. Epub 2011 Jun 10. Am J Med Genet A. 2011. PMID: 21671391
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder.
Zollino M, Orteschi D, Ruiter M, Pfundt R, Steindl K, Cafiero C, Ricciardi S, Contaldo I, Chieffo D, Ranalli D, Acquafondata C, Murdolo M, Marangi G, Asaro A, Battaglia D. Zollino M, et al. Among authors: murdolo m. Epilepsia. 2014 Jun;55(6):849-57. doi: 10.1111/epi.12617. Epub 2014 Apr 16. Epilepsia. 2014. PMID: 24738919 Free article.
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome.
Cafiero C, Marangi G, Orteschi D, Ali M, Asaro A, Ponzi E, Moncada A, Ricciardi S, Murdolo M, Mancano G, Contaldo I, Leuzzi V, Battaglia D, Mercuri E, Slavotinek AM, Zollino M. Cafiero C, et al. Among authors: murdolo m. Eur J Hum Genet. 2015 Nov;23(11):1499-504. doi: 10.1038/ejhg.2015.19. Epub 2015 Feb 25. Eur J Hum Genet. 2015. PMID: 25712080 Free PMC article.
26 results