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

Year Number of Results
2006 1
2007 2
2009 1
2011 1
2017 2
2018 1
2020 2
2021 3
2022 2
2023 3
2024 2

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18 results

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Page 1
Chemotherapy-associated paronychia: Do not forget the children.
Borgia P, Piccolo G, Diana MC, Viglizzo G. Borgia P, et al. Among authors: diana mc. J Am Acad Dermatol. 2023 Jan;88(1):e59. doi: 10.1016/j.jaad.2022.09.045. Epub 2022 Oct 4. J Am Acad Dermatol. 2023. PMID: 36206933 No abstract available.
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: diana mc. Cancers (Basel). 2023 Mar 22;15(6):1916. doi: 10.3390/cancers15061916. Cancers (Basel). 2023. PMID: 36980803 Free PMC article.
Listeria Meningitis in an Immunocompetent Child.
Villa G, Diana MC, Solari N, Bandettini R, Sorrentino S, Loy A, Losurdo G, Renna S. Villa G, et al. Among authors: diana mc. Pediatr Emerg Care. 2017 Aug;33(8):579-581. doi: 10.1097/PEC.0000000000000687. Pediatr Emerg Care. 2017. PMID: 27055168
Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders.
Borgia P, Baldassari S, Pedemonte N, Alkhunaizi E, D'Onofrio G, Tortora D, Calì E, Scudieri P, Balagura G, Musante I, Diana MC, Pedemonte M, Vari MS, Iacomino M, Riva A, Chimenz R, Mangano GD, Mohammadi MH, Toosi MB, Ashrafzadeh F, Imannezhad S, Karimiani EG, Accogli A, Schiaffino MC, Maghnie M, Soler MA, Echiverri K, Abrams CK, Striano P, Fortuna S, Maroofian R, Houlden H, Zara F, Fiorillo C, Salpietro V. Borgia P, et al. Among authors: diana mc. Orphanet J Rare Dis. 2022 Jul 19;17(1):286. doi: 10.1186/s13023-022-02415-5. Orphanet J Rare Dis. 2022. PMID: 35854306 Free PMC article.
Anterior chest wall deformities in children with neurofibromatosis type 1.
Chelleri C, Guerriero V, Torre M, Brolatti N, Piccolo G, Mattioli G, Boero S, Minetti C, Diana MC. Chelleri C, et al. Among authors: diana mc. Acta Paediatr. 2021 Feb;110(2):594-595. doi: 10.1111/apa.15529. Epub 2020 Aug 29. Acta Paediatr. 2021. PMID: 32777120 No abstract available.
Genotype-Phenotype Correlations in Neurofibromatosis Type 1: A Single-Center Cohort Study.
Scala M, Schiavetti I, Madia F, Chelleri C, Piccolo G, Accogli A, Riva A, Salpietro V, Bocciardi R, Morcaldi G, Di Duca M, Caroli F, Verrico A, Milanaccio C, Viglizzo G, Traverso M, Baldassari S, Scudieri P, Iacomino M, Piatelli G, Minetti C, Striano P, Garrè ML, De Marco P, Diana MC, Capra V, Pavanello M, Zara F. Scala M, et al. Among authors: diana mc. Cancers (Basel). 2021 Apr 14;13(8):1879. doi: 10.3390/cancers13081879. Cancers (Basel). 2021. PMID: 33919865 Free PMC article.
RNF213 variant in a patient with Legius syndrome associated with moyamoya syndrome.
Romanisio G, Chelleri C, Scala M, Piccolo G, Carlini B, Gatti L, Capra V, Zara F, Bersano A, Pavanello M, De Marco P, Diana MC. Romanisio G, et al. Among authors: diana mc. Mol Genet Genomic Med. 2021 Jun;9(6):e1669. doi: 10.1002/mgg3.1669. Epub 2021 May 3. Mol Genet Genomic Med. 2021. PMID: 33939317 Free PMC article. No abstract available.
[Guidelines on acute otitis media].
Marchisio P, Principi N, Bellussi L; Gruppo di Stesura. Marchisio P, et al. Minerva Pediatr. 2009 Dec;61(6):885-6. Minerva Pediatr. 2009. PMID: 19935583 Italian. No abstract available.
18 results