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

Year Number of Results
1971 1
1972 1
1973 2
1976 1
2004 2
2005 1
2007 1
2008 1
2009 1
2010 3
2011 1
2013 1
2014 1
2017 1
2018 1
2019 1
2020 1
2021 2
2022 1
2023 0
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22 results
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Page 1
In vivo imaging of calcium dynamics in zebrafish hepatocytes.
Pozo-Morales M, Garteizgogeascoa I, Perazzolo C, So J, Shin D, Singh SP. Pozo-Morales M, et al. Among authors: perazzolo c. Hepatology. 2022 Jul 13. doi: 10.1002/hep.32663. Online ahead of print. Hepatology. 2022. PMID: 35829917
Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy.
Duerinckx S, Désir J, Perazzolo C, Badoer C, Jacquemin V, Soblet J, Maystadt I, Tunca Y, Blaumeiser B, Ceulemans B, Courtens W, Debray FG, Destree A, Devriendt K, Jansen A, Keymolen K, Lederer D, Loeys B, Meuwissen M, Moortgat S, Mortier G, Nassogne MC, Sekhara T, Van Coster R, Van Den Ende J, Van der Aa N, Van Esch H, Vanakker O, Verhelst H, Vilain C, Weckhuysen S, Passemard S, Verloes A, Aeby A, Deconinck N, Van Bogaert P, Pirson I, Abramowicz M. Duerinckx S, et al. Among authors: perazzolo c. Mol Genet Genomic Med. 2021 Sep;9(9):e1768. doi: 10.1002/mgg3.1768. Epub 2021 Aug 17. Mol Genet Genomic Med. 2021. PMID: 34402213 Free PMC article.
TrkA mediates effect of novel KIDINS220 mutation in human brain ventriculomegaly.
Jacquemin V, Antoine M, Duerinckx S, Massart A, Desir J, Perazzolo C, Cassart M, Thomas D, Segers V, Lecomte S, Abramowicz M, Pirson I. Jacquemin V, et al. Among authors: perazzolo c. Hum Mol Genet. 2021 Feb 4;29(23):3757-3764. doi: 10.1093/hmg/ddaa245. Hum Mol Genet. 2021. PMID: 33205811
Digenic inheritance of human primary microcephaly delineates centrosomal and non-centrosomal pathways.
Duerinckx S, Jacquemin V, Drunat S, Vial Y, Passemard S, Perazzolo C, Massart A, Soblet J, Racapé J, Desmyter L, Badoer C, Papadimitriou S, Le Borgne YA, Lefort A, Libert F, De Maertelaer V, Rooman M, Costagliola S, Verloes A, Lenaerts T, Pirson I, Abramowicz M. Duerinckx S, et al. Among authors: perazzolo c. Hum Mutat. 2020 Feb;41(2):512-524. doi: 10.1002/humu.23948. Epub 2019 Nov 27. Hum Mutat. 2020. PMID: 31696992 Free PMC article.
Severe congenital microcephaly with AP4M1 mutation, a case report.
Duerinckx S, Verhelst H, Perazzolo C, David P, Desmyter L, Pirson I, Abramowicz M. Duerinckx S, et al. Among authors: perazzolo c. BMC Med Genet. 2017 May 2;18(1):48. doi: 10.1186/s12881-017-0412-9. BMC Med Genet. 2017. PMID: 28464862 Free PMC article.
The ribosome cycle in bacteria.
Algranati ID, González NS, García-Patrone M, Perazzolo CA, Azzam ME. Algranati ID, et al. Among authors: perazzolo ca. Basic Life Sci. 1973;1:327-38. doi: 10.1007/978-1-4684-0877-5_27. Basic Life Sci. 1973. PMID: 4589685 Review. No abstract available.
Hyperpolarized lithium-6 as a sensor of nanomolar contrast agents.
van Heeswijk RB, Uffmann K, Comment A, Kurdzesau F, Perazzolo C, Cudalbu C, Jannin S, Konter JA, Hautle P, van den Brandt B, Navon G, van der Klink JJ, Gruetter R. van Heeswijk RB, et al. Among authors: perazzolo c. Magn Reson Med. 2009 Jun;61(6):1489-93. doi: 10.1002/mrm.21952. Magn Reson Med. 2009. PMID: 19353663 Free PMC article.
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
Simonis N, Migeotte I, Lambert N, Perazzolo C, de Silva DC, Dimitrov B, Heinrichs C, Janssens S, Kerr B, Mortier G, Van Vliet G, Lepage P, Casimir G, Abramowicz M, Smits G, Vilain C. Simonis N, et al. Among authors: perazzolo c. J Med Genet. 2013 Sep;50(9):585-92. doi: 10.1136/jmedgenet-2013-101603. Epub 2013 Jun 28. J Med Genet. 2013. PMID: 23812909 Free PMC article.
22 results