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

Year Number of Results
2006 5
2007 2
2008 1
2009 2
2010 1
2011 4
2012 1
2013 2
2014 2
2015 5
2016 7
2017 8
2018 13
2019 10
2020 26
2021 19
2022 12
2023 14
2024 6

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116 results

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Page 1
Chiari malformation type I: what information from the genetics?
Capra V, Iacomino M, Accogli A, Pavanello M, Zara F, Cama A, De Marco P. Capra V, et al. Among authors: pavanello m. Childs Nerv Syst. 2019 Oct;35(10):1665-1671. doi: 10.1007/s00381-019-04322-w. Epub 2019 Aug 5. Childs Nerv Syst. 2019. PMID: 31385087 Review.
Moyamoya Vasculopathy in Neurofibromatosis Type 1 Pediatric Patients: The Role of Rare Variants of RNF213.
Ognibene M, Scala M, Iacomino M, Schiavetti I, Madia F, Traverso M, Guerrisi S, Di Duca M, Caroli F, Baldassari S, Tappino B, Romano F, Uva P, Vozzi D, Chelleri C, Piatelli G, Diana MC, Zara F, Capra V, Pavanello M, De Marco P. Ognibene M, et al. Among authors: pavanello m. Cancers (Basel). 2023 Mar 22;15(6):1916. doi: 10.3390/cancers15061916. Cancers (Basel). 2023. PMID: 36980803 Free PMC article.
Expanding the phenotype associated with biallelic SLC20A2 variants.
D'Onofrio G, Scala M, Severino M, Roberti R, Romano F, De Marco P, Iacomino M, Baldassari S, Uva P, Pavanello M, Gustincich S, Striano P, Zara F, Capra V. D'Onofrio G, et al. Among authors: pavanello m. Eur J Hum Genet. 2023 Jul;31(7):725-729. doi: 10.1038/s41431-023-01349-1. Epub 2023 Mar 28. Eur J Hum Genet. 2023. PMID: 36977836 No abstract available.
Imaging characteristics and neurosurgical outcome in subjects with agenesis of the corpus callosum and interhemispheric cysts.
Severino M, Tortora D, Reid C, Uccella S, Nobili L, Accogli A, Srour M, Ramaglia A, Sudhakar S, Consales A, Pavanello M, Piatelli G, James G, Ravegnani M, Rossi A, Mankad K. Severino M, et al. Among authors: pavanello m. Neuroradiology. 2022 Nov;64(11):2163-2177. doi: 10.1007/s00234-022-02990-1. Epub 2022 Jun 7. Neuroradiology. 2022. PMID: 35670822 Review.
116 results