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

Year Number of Results
1992 1
1993 2
1998 2
1999 1
2000 1
2001 2
2002 1
2003 2
2006 1
2007 3
2008 2
2009 3
2010 1
2011 4
2012 3
2013 4
2014 5
2015 2
2016 3
2017 1
2018 2
2020 1
2024 0

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41 results

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Page 1
A rare case of bladder diverticulosis.
Saruggia M, Cabrelle G, Poggiani C, Barletta A, Sironi S. Saruggia M, et al. Among authors: poggiani c. Clin Imaging. 2020 Sep;65:33-36. doi: 10.1016/j.clinimag.2020.04.013. Epub 2020 Apr 18. Clin Imaging. 2020. PMID: 32353716
Brain ultrasound in Canavan disease.
Drera B, Poggiani C. Drera B, et al. Among authors: poggiani c. J Ultrasound. 2014 Jun 21;17(3):215-7. doi: 10.1007/s40477-014-0108-3. eCollection 2014 Sep. J Ultrasound. 2014. PMID: 25177395 Free PMC article.
Survey of neonatal respiratory support use in very preterm infants in Italy.
Gagliardi L, Tagliabue P, Bellù R, Corchia C, Mosca F, Zanini R; Network Neonatale Italiano. Gagliardi L, et al. J Matern Fetal Neonatal Med. 2012 Oct;25 Suppl 3:1-5. doi: 10.3109/14767058.2012.712310. J Matern Fetal Neonatal Med. 2012. PMID: 23016609 Free article. Review.
The Italian Horizon Scanning Project.
Joppi R, Demattè L, Menti AM, Pase D, Poggiani C, Mezzalira L; Italian Horizon Scanning Project Group. Joppi R, et al. Among authors: poggiani c. Eur J Clin Pharmacol. 2009 Aug;65(8):775-81. doi: 10.1007/s00228-009-0666-z. Epub 2009 Jun 3. Eur J Clin Pharmacol. 2009. PMID: 19495735 Free article. No abstract available.
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.
Lionel AC, Tammimies K, Vaags AK, Rosenfeld JA, Ahn JW, Merico D, Noor A, Runke CK, Pillalamarri VK, Carter MT, Gazzellone MJ, Thiruvahindrapuram B, Fagerberg C, Laulund LW, Pellecchia G, Lamoureux S, Deshpande C, Clayton-Smith J, White AC, Leather S, Trounce J, Melanie Bedford H, Hatchwell E, Eis PS, Yuen RK, Walker S, Uddin M, Geraghty MT, Nikkel SM, Tomiak EM, Fernandez BA, Soreni N, Crosbie J, Arnold PD, Schachar RJ, Roberts W, Paterson AD, So J, Szatmari P, Chrysler C, Woodbury-Smith M, Brian Lowry R, Zwaigenbaum L, Mandyam D, Wei J, Macdonald JR, Howe JL, Nalpathamkalam T, Wang Z, Tolson D, Cobb DS, Wilks TM, Sorensen MJ, Bader PI, An Y, Wu BL, Musumeci SA, Romano C, Postorivo D, Nardone AM, Monica MD, Scarano G, Zoccante L, Novara F, Zuffardi O, Ciccone R, Antona V, Carella M, Zelante L, Cavalli P, Poggiani C, Cavallari U, Argiropoulos B, Chernos J, Brasch-Andersen C, Speevak M, Fichera M, Ogilvie CM, Shen Y, Hodge JC, Talkowski ME, Stavropoulos DJ, Marshall CR, Scherer SW. Lionel AC, et al. Among authors: poggiani c. Hum Mol Genet. 2014 May 15;23(10):2752-68. doi: 10.1093/hmg/ddt669. Epub 2013 Dec 30. Hum Mol Genet. 2014. PMID: 24381304 Free PMC article.
Pictorial essay of Werdnig-Hoffman disease.
Poggiani C, Ferrari D, Parati S, Torresani P. Poggiani C, et al. Minerva Pediatr. 2009 Apr;61(2):237-8. Minerva Pediatr. 2009. PMID: 19322128 No abstract available.
Prenatal exclusion of cleidocranial dysplasia.
Cavalli P, Santorelli FM, Bontardelli M, Tessa A, Bosi A, Poggiani C. Cavalli P, et al. Among authors: poggiani c. Prenat Diagn. 2003 Nov;23(11):945-6. doi: 10.1002/pd.718. Prenat Diagn. 2003. PMID: 14634985 No abstract available.
41 results