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Items: 16

1.

Characterization of intellectual disability and autism comorbidity through gene panel sequencing.

Aspromonte MC, Bellini M, Gasparini A, Carraro M, Bettella E, Polli R, Cesca F, Bigoni S, Boni S, Carlet O, Negrin S, Mammi I, Milani D, Peron A, Sartori S, Toldo I, Soli F, Turolla L, Stanzial F, Benedicenti F, Marino-Buslje C, Tosatto SCE, Murgia A, Leonardi E.

Hum Mutat. 2019 Sep;40(9):1346-1363. doi: 10.1002/humu.23822. Epub 2019 Aug 2.

PMID:
31209962
2.

Small supernumerary marker chromosomes: A legacy of trisomy rescue?

Kurtas NE, Xumerle L, Leonardelli L, Delledonne M, Brusco A, Chrzanowska K, Schinzel A, Larizza D, Guerneri S, Natacci F, Bonaglia MC, Reho P, Manolakos E, Mattina T, Soli F, Provenzano A, Al-Rikabi AH, Errichiello E, Nazaryan-Petersen L, Giglio S, Tommerup N, Liehr T, Zuffardi O.

Hum Mutat. 2019 Feb;40(2):193-200. doi: 10.1002/humu.23683. Epub 2018 Nov 22.

PMID:
30412329
3.

A novel mutation in ABCD1 unveils different clinical phenotypes in a family with adrenoleukodystrophy.

Margoni M, Soli F, Sangalli A, Bellizzi M, Cecchini E, Buganza M.

J Clin Neurosci. 2017 Sep;43:175-177. doi: 10.1016/j.jocn.2017.05.025. Epub 2017 Jun 7.

PMID:
28601575
4.

Effect of oral contraceptives and doxycycline on endometrial MMP-2 and MMP-9 activity.

Kaneshiro B, Edelman A, Dash C, Pandhare J, Soli FM, Jensen JT.

Contraception. 2016 Jan;93(1):65-9. doi: 10.1016/j.contraception.2015.09.006. Epub 2015 Sep 25.

5.

Frequency of estrogen receptor (ER)-negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the so-called triple-negative phenotype: a population-based study from Trentino, North East Italy.

Giuliani S, Leonardi E, Aldovini D, Bernardi D, Pellegrini M, Soli F, Ferro A, Dalla Palma P, Decarli N, Barbareschi M.

Pathologica. 2012 Jun;104(3):93-7.

PMID:
22931039
6.

De novo unbalanced translocations in Prader-Willi and Angelman syndrome might be the reciprocal product of inv dup(15)s.

Rossi E, Giorda R, Bonaglia MC, Candia SD, Grechi E, Franzese A, Soli F, Rivieri F, Patricelli MG, Saccilotto D, Bonfante A, Giglio S, Beri S, Rocchi M, Zuffardi O.

PLoS One. 2012;7(6):e39180. doi: 10.1371/journal.pone.0039180. Epub 2012 Jun 14.

7.

Monitoring the multi-faceted problem of youth violence: the Asian/Pacific Islander Youth Violence Prevention Center's surveillance system.

Sugimoto-Matsuda JJ, Hishinuma ES, Momohara CB, Rehuher D, Soli FM, Bautista RP, Chang JY.

J Community Health. 2012 Oct;37(5):1015-25. doi: 10.1007/s10900-011-9525-9.

PMID:
22231577
8.

Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management.

Grandone E, Tiscia G, Cappucci F, Favuzzi G, Santacroce R, Pisanelli D, Soli F, Legnani C, Rizzo MA, Palareti G, Margaglione M.

Haemophilia. 2012 Jan;18(1):e16-8. doi: 10.1111/j.1365-2516.2011.02656.x. Epub 2011 Oct 10. No abstract available.

PMID:
21981355
9.

Community perceptions of safety in relation to perceived youth violence-delinquency in a primarily native Hawaiian and Asian American community in Hawai'i.

Hishinuma ES, Chang JY, Soli FM.

J Community Health. 2012 Feb;37(1):123-36. doi: 10.1007/s10900-011-9426-y.

PMID:
21667344
10.

Administration of copper oxide wire particles in a capsule or feed for gastrointestinal nematode control in goats.

Burke JM, Soli F, Miller JE, Terrill TH, Wildeus S, Shaik SA, Getz WR, Vanguru M.

Vet Parasitol. 2010 Mar 25;168(3-4):346-50. doi: 10.1016/j.vetpar.2009.10.027. Epub 2009 Nov 10.

PMID:
19945224
11.

Efficacy of copper oxide wire particles against gastrointestinal nematodes in sheep and goats.

Soli F, Terrill TH, Shaik SA, Getz WR, Miller JE, Vanguru M, Burke JM.

Vet Parasitol. 2010 Feb 26;168(1-2):93-6. doi: 10.1016/j.vetpar.2009.10.004. Epub 2009 Oct 29.

PMID:
19931291
12.

Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.

Garavelli L, Zollino M, Mainardi PC, Gurrieri F, Rivieri F, Soli F, Verri R, Albertini E, Favaron E, Zignani M, Orteschi D, Bianchi P, Faravelli F, Forzano F, Seri M, Wischmeijer A, Turchetti D, Pompilii E, Gnoli M, Cocchi G, Mazzanti L, Bergamaschi R, De Brasi D, Sperandeo MP, Mari F, Uliana V, Mostardini R, Cecconi M, Grasso M, Sassi S, Sebastio G, Renieri A, Silengo M, Bernasconi S, Wakamatsu N, Neri G.

Am J Med Genet A. 2009 Mar;149A(3):417-26. doi: 10.1002/ajmg.a.32693. Review.

PMID:
19215041
13.

Holt-Oram syndrome associated with anomalies of the feet.

Garavelli L, De Brasi D, Verri R, Guareschi E, Cariola F, Melis D, Calcagno G, Salvatore F, Unger S, Sebastio G, Albertini G, Rivieri F, Soli F, Superti-Furga A, Gentile M.

Am J Med Genet A. 2008 May 1;146A(9):1185-9. doi: 10.1002/ajmg.a.32170.

PMID:
18351627
14.

Terminal osseous dysplasia with pigmentary defects: clinical description of a new family.

Baroncini A, Castelluccio P, Morleo M, Soli F, Franco B.

Am J Med Genet A. 2007 Jan 1;143A(1):51-7.

PMID:
17152064
15.

Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndrome.

Kenwrick S, Woffendin H, Jakins T, Shuttleworth SG, Mayer E, Greenhalgh L, Whittaker J, Rugolotto S, Bardaro T, Esposito T, D'Urso M, Soli F, Turco A, Smahi A, Hamel-Teillac D, Lyonnet S, Bonnefont JP, Munnich A, Aradhya S, Kashork CD, Shaffer LG, Nelson DL, Levy M, Lewis RA; International IP Consortium.

Am J Hum Genet. 2001 Dec;69(6):1210-7. Epub 2001 Oct 22.

16.

Haemodynamic changes in the subclavian steal syndrome.

Soli F, Iskum M, Zádory E, Hartal A, Nagy J, Rév J.

Acta Med Acad Sci Hung. 1968;25(1):79-86. No abstract available.

PMID:
5678742

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