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Terminal deletion of the long arm of chromosome 10.
Scigliano S, Grégoire MJ, Schmitt M, Jonveaux PH, LeHeup B. Scigliano S, et al. Clin Genet. 2004 Apr;65(4):294-8. doi: 10.1111/j.1399-0004.2004.00218.x. Clin Genet. 2004. PMID: 15025722 Review.
Late Diagnosis of Infants with PCD and Neonatal Respiratory Distress.
Goutaki M, Halbeisen FS, Barbato A, Crowley S, Harris A, Hirst RA, Karadag B, Martinu V, Morgan L, O'Callaghan C, Ozçelik U, Scigliano S, Ucros S, Yiallouros P, Schulzke SM, Kuehni CE. Goutaki M, et al. Among authors: scigliano s. J Clin Med. 2020 Sep 4;9(9):2871. doi: 10.3390/jcm9092871. J Clin Med. 2020. PMID: 32899853 Free PMC article.
The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results.
Goutaki M, Maurer E, Halbeisen FS, Amirav I, Barbato A, Behan L, Boon M, Casaulta C, Clement A, Crowley S, Haarman E, Hogg C, Karadag B, Koerner-Rettberg C, Leigh MW, Loebinger MR, Mazurek H, Morgan L, Nielsen KG, Omran H, Schwerk N, Scigliano S, Werner C, Yiallouros P, Zivkovic Z, Lucas JS, Kuehni CE; PCD Italian Consortium; Swiss PCD Group; French Reference Centre for Rare Lung Diseases; Genetic Disorders of Mucociliary Clearance Consortium. Goutaki M, et al. Among authors: scigliano s. Eur Respir J. 2017 Jan 4;49(1):1601181. doi: 10.1183/13993003.01181-2016. Print 2017 Jan. Eur Respir J. 2017. PMID: 28052956 Free PMC article.
18F-FDG PET/CT in the characterization and surgical decision concerning adrenal masses: a prospective multicentre evaluation.
Ansquer C, Scigliano S, Mirallié E, Taïeb D, Brunaud L, Sebag F, Leux C, Drui D, Dupas B, Renaudin K, Kraeber-Bodéré F. Ansquer C, et al. Among authors: scigliano s. Eur J Nucl Med Mol Imaging. 2010 Aug;37(9):1669-78. doi: 10.1007/s00259-010-1471-8. Epub 2010 May 19. Eur J Nucl Med Mol Imaging. 2010. PMID: 20490488 Clinical Trial.