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

Year Number of Results
2008 1
2011 1
2014 3
2015 3
2016 1
2017 3
2018 3
2019 6
2020 4
2021 2
2022 5
2023 6
2024 2

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38 results

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Page 1
Prenatal Clinical Findings in RASA1-Related Capillary Malformation-Arteriovenous Malformation Syndrome.
Coccia E, Valeri L, Zuntini R, Caraffi SG, Peluso F, Pagliai L, Vezzani A, Pietrangiolillo Z, Leo F, Melli N, Fiorini V, Greco A, Lepri FR, Pisaneschi E, Marozza A, Carli D, Mussa A, Radio FC, Conti B, Iascone M, Gargano G, Novelli A, Tartaglia M, Zuffardi O, Bedeschi MF, Garavelli L. Coccia E, et al. Among authors: pisaneschi e. Genes (Basel). 2023 Feb 22;14(3):549. doi: 10.3390/genes14030549. Genes (Basel). 2023. PMID: 36980822 Free PMC article.
Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study.
Diociaiuti A, Rotunno R, Pisaneschi E, Cesario C, Carnevale C, Condorelli AG, Rollo M, Di Cecca S, Quintarelli C, Novelli A, Zambruno G, El Hachem M. Diociaiuti A, et al. Among authors: pisaneschi e. Biomedicines. 2022 Jun 20;10(6):1460. doi: 10.3390/biomedicines10061460. Biomedicines. 2022. PMID: 35740480 Free PMC article.
Next generation sequencing panel target genes: possible diagnostic tool for ectodermal dysplasia related diseases.
Callea M, Bellacchio E, Cammarata Scalisi F, El Feghaly J, El-Ghandour RK, Avendaño A, Yavuz Y, Diociaiuti A, Digilio MC, DI Stazio M, Novelli A, Oranges T, Filippeschi C, Pisaneschi E, Jilani H, Gigola F, Willoughby CE, Morabito A. Callea M, et al. Among authors: pisaneschi e. Ital J Dermatol Venerol. 2023 Feb;158(1):32-38. doi: 10.23736/S2784-8671.23.07540-0. Ital J Dermatol Venerol. 2023. PMID: 36939501 Free article.
Angioma serpiginosum: a case report and review of the literature.
Diociaiuti A, Cutrone M, Rotunno R, De Vito R, Neri I, Pisaneschi E, El Hachem M. Diociaiuti A, et al. Among authors: pisaneschi e. Ital J Pediatr. 2019 Apr 27;45(1):53. doi: 10.1186/s13052-019-0644-8. Ital J Pediatr. 2019. PMID: 31029177 Free PMC article. Review.
Kabuki syndrome: clinical and molecular diagnosis in the first year of life.
Dentici ML, Di Pede A, Lepri FR, Gnazzo M, Lombardi MH, Auriti C, Petrocchi S, Pisaneschi E, Bellacchio E, Capolino R, Braguglia A, Angioni A, Dotta A, Digilio MC, Dallapiccola B. Dentici ML, et al. Among authors: pisaneschi e. Arch Dis Child. 2015 Feb;100(2):158-64. doi: 10.1136/archdischild-2013-305858. Epub 2014 Oct 3. Arch Dis Child. 2015. PMID: 25281733 Review.
PIK3CA-related overgrowth with an uncommon phenotype: case report.
Rotunno R, Diociaiuti A, Pisaneschi E, Carnevale C, Dentici M, El Hachem M. Rotunno R, et al. Among authors: pisaneschi e. Ital J Pediatr. 2022 May 12;48(1):71. doi: 10.1186/s13052-022-01268-9. Ital J Pediatr. 2022. PMID: 35551640 Free PMC article.
Surgical management of pediatric intracranial CCM: a 10-year single center experience.
Calloni T, Carai A, Lioi F, Cavaliere M, DE Benedictis A, Rossi S, Randi F, Rossi Espagnet MC, Trivisano M, Cesario C, Pisaneschi E, Marasi A, Savioli A, Giussani CG, Marras CE. Calloni T, et al. Among authors: pisaneschi e. J Neurosurg Sci. 2022 Apr 13. doi: 10.23736/S0390-5616.22.05574-6. Online ahead of print. J Neurosurg Sci. 2022. PMID: 35416451
Novel clinical features associated with Clouston syndrome.
Cammarata-Scalisi F, Rinelli M, Pisaneschi E, Diociaiuti A, Willoughby CE, Avendaño A, Digilio MC, Novelli A, Callea M. Cammarata-Scalisi F, et al. Among authors: pisaneschi e. Int J Dermatol. 2019 Aug;58(8):e143-e146. doi: 10.1111/ijd.14507. Epub 2019 Jun 5. Int J Dermatol. 2019. PMID: 31165482 No abstract available.
TRAPPC9-CDG: A novel congenital disorder of glycosylation with dysmorphic features and intellectual disability.
Radenkovic S, Martinelli D, Zhang Y, Preston GJ, Maiorana A, Terracciano A, Dentici ML, Pisaneschi E, Novelli A, Ranatunga W, Ligezka AN, Ghesquière B, Deyle DR, Kozicz T, Pinto E Vairo F, Witters P, Morava E. Radenkovic S, et al. Among authors: pisaneschi e. Genet Med. 2022 Apr;24(4):894-904. doi: 10.1016/j.gim.2021.12.012. Epub 2022 Jan 15. Genet Med. 2022. PMID: 35042660 Free article.
38 results