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Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature.
Epilepsia. 2012 Jul;53(7):1146-55. doi: 10.1111/j.1528-1167.2012.03501.x. Epub 2012 May 11.
Epilepsia. 2012.
PMID: 22578097
Free article.
Review.
Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletion.
Torniero C, Dalla Bernardina B, Novara F, Cerini R, Bonaglia C, Pramparo T, Ciccone R, Guerrini R, Zuffardi O.
Torniero C, et al. Among authors: bonaglia c.
Eur J Hum Genet. 2008 Aug;16(8):880-7. doi: 10.1038/ejhg.2008.42. Epub 2008 Mar 12.
Eur J Hum Genet. 2008.
PMID: 18337728
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The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.
Floridia G, Piantanida M, Minelli A, Dellavecchia C, Bonaglia C, Rossi E, Gimelli G, Croci G, Franchi F, Gilgenkrantz S, Grammatico P, Dalprá L, Wood S, Danesino C, Zuffardi O.
Floridia G, et al. Among authors: bonaglia c.
Am J Hum Genet. 1996 Apr;58(4):785-96.
Am J Hum Genet. 1996.
PMID: 8644743
Free PMC article.
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Ring chromosome 9: an atypical case.
Lanzi G, Fazzi E, Veggiotti P, Pagliano E, Gariglio M, Bonaglia C, Landolfo S.
Lanzi G, et al. Among authors: bonaglia c.
Brain Dev. 1996 May-Jun;18(3):216-9. doi: 10.1016/0387-7604(95)00144-1.
Brain Dev. 1996.
PMID: 8836504
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A prenatal case with multiple supernumerary markers identified as derivatives of chromosomes 13, 15, and 20: molecular cytogenetic characterization and review of the literature.
Bertini V, Giuliani C, Ferreri MI, Orsini A, Bonuccelli A, Peroni D, Bonaglia C, Valetto A.
Bertini V, et al. Among authors: bonaglia c.
J Matern Fetal Neonatal Med. 2021 Sep;34(17):2918-2922. doi: 10.1080/14767058.2019.1670808. Epub 2019 Oct 1.
J Matern Fetal Neonatal Med. 2021.
PMID: 31570022
Review.
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UCRAID (Ukrainian Citizen and refugee electronic support in Respiratory diseases, Allergy, Immunology and Dermatology) action plan.
Bousquet J, Samolinski B, Kaidashev I, Maurer M, Roche N, Sousa-Pinto B, Kurchenko A, Stepanenko R, Tsaryk V, Klimek L, Ventura MT, Bedbrook A, Czarlewski W, Lysanets Y, Kupczyk M, Skolimowski Ł, Kulus M, Del Giacco S, Ollert M, Garcia-Aymerich J, Robalo Cordeiro C, Yorgancioglu A, Schlapbach C, Amaral R, Bonaglia C, Bossé I, Buquicchio R, Christou D, Fedoruk G, Fontanesi P, Gemicioglu B, Giuliano AFM, Lepore P, Nakonechna A, Neisinger S, Pereira AM, Ramanauskaite A, Raciborski F, Sitkauskiene B, Sokhatska O, Stepanenko V, Stevanovic K, Syzon O, Kvedariene V, de Vries G, van Eerd M, Valiulis A, Fonseca JA, Anto JM, Haahtela T, Schünemann H, Zuberbier T.
Bousquet J, et al. Among authors: bonaglia c.
Allergy. 2023 Oct;78(10):2581-2595. doi: 10.1111/all.15855. Epub 2023 Aug 28.
Allergy. 2023.
PMID: 37641384
Free article.
Review.
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Genetic correction of human induced pluripotent stem cells from patients with spinal muscular atrophy.
Corti S, Nizzardo M, Simone C, Falcone M, Nardini M, Ronchi D, Donadoni C, Salani S, Riboldi G, Magri F, Menozzi G, Bonaglia C, Rizzo F, Bresolin N, Comi GP.
Corti S, et al. Among authors: bonaglia c.
Sci Transl Med. 2012 Dec 19;4(165):165ra162. doi: 10.1126/scitranslmed.3004108.
Sci Transl Med. 2012.
PMID: 23253609
Free PMC article.
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