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Items: 1 to 50 of 100

1.

S100B as a new fecal biomarker of inflammatory bowel diseases.

Di Liddo R, Piccione M, Schrenk S, Dal Magro C, Cosma C, Padoan A, Contran N, Scapellato ML, Pagetta A, Romano Spica V, Conconi MT, Parnigotto PP, D'Incà R, Michetti F.

Eur Rev Med Pharmacol Sci. 2020 Jan;24(1):323-332. doi: 10.26355/eurrev_202001_19929.

PMID:
31957846
2.

Infrapatellar Fat Pad Stem Cells Responsiveness to Microenvironment in Osteoarthritis: From Morphology to Function.

Stocco E, Barbon S, Piccione M, Belluzzi E, Petrelli L, Pozzuoli A, Ramonda R, Rossato M, Favero M, Ruggieri P, Porzionato A, Di Liddo R, De Caro R, Macchi V.

Front Cell Dev Biol. 2019 Dec 10;7:323. doi: 10.3389/fcell.2019.00323. eCollection 2019.

3.

Wnt signaling regulates the proliferation potential and lineage commitment of human umbilical cord derived mesenchymal stem cells.

Jothimani G, Di Liddo R, Pathak S, Piccione M, Sriramulu S, Banerjee A.

Mol Biol Rep. 2020 Feb;47(2):1293-1308. doi: 10.1007/s11033-019-05232-5. Epub 2019 Dec 18.

PMID:
31853765
4.

Serum IgE against cross-reactive carbohydrate determinants (CCD) in healthy and atopic dogs.

Piccione ML, DeBoer DJ.

Vet Dermatol. 2019 Dec;30(6):507-e153. doi: 10.1111/vde.12799. Epub 2019 Oct 22.

PMID:
31642119
5.

New Onset Right Bundle Branch Block In Acute Coronary Syndrome and High-Grade Stenosis: A Case Series.

Shaikh S, Al-Sadawi M, Dogar MU, Cavusoglu E, Hegde S, Salciccioli L, Piccione M, Abrahim C, Yacoub M, Ponce D, McFarlane SI.

Scifed J Cardiol. 2019;3(1). pii: 23. Epub 2019 Mar 13.

6.

Congenital emphysematous lung disease associated with a novel Filamin A mutation. Case report and literature review.

Pelizzo G, Collura M, Puglisi A, Pappalardo MP, Agolini E, Novelli A, Piccione M, Cacace C, Bussani R, Corsello G, Calcaterra V.

BMC Pediatr. 2019 Mar 29;19(1):86. doi: 10.1186/s12887-019-1460-4.

7.

Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein-Taybi syndrome: the interconnections of epigenetic machinery disorders.

Negri G, Magini P, Milani D, Crippa M, Biamino E, Piccione M, Sotgiu S, Perrìa C, Vitiello G, Frontali M, Boni A, Di Fede E, Gandini MC, Colombo EA, Bamshad MJ, Nickerson DA, Smith JD, Loddo I, Finelli P, Seri M, Pippucci T, Larizza L, Gervasini C.

Hum Genet. 2019 Mar;138(3):257-269. doi: 10.1007/s00439-019-01985-y. Epub 2019 Feb 26.

8.

Type IV Laryngotracheoesophageal Cleft Associated with Type III Esophageal Atresia in 1p36 Deletions Containing the RERE Gene: Is There a Causal Role for the Genetic Alteration?

Pelizzo G, Puglisi A, Lapi M, Piccione M, Matina F, Busè M, Mura GB, Re G, Calcaterra V.

Case Rep Pediatr. 2018 Aug 29;2018:4060527. doi: 10.1155/2018/4060527. eCollection 2018.

9.

Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1.

Corsello G, Antona V, Serra G, Zara F, Giambrone C, Lagalla L, Piccione M, Piro E.

Ital J Pediatr. 2018 Apr 4;44(1):45. doi: 10.1186/s13052-018-0483-z.

10.

Impairment of elastic properties of the aorta in bicuspid aortic valve: relationship between biomolecular and aortic strain patterns.

Longobardo L, Carerj ML, Pizzino G, Bitto A, Piccione MC, Zucco M, Oreto L, Todaro MC, Calabrò MP, Squadrito F, Di Bella G, Oreto G, Khandheria BK, Carerj S, Zito C.

Eur Heart J Cardiovasc Imaging. 2018 Aug 1;19(8):879-887. doi: 10.1093/ehjci/jex224.

PMID:
29029085
11.

Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series.

Busè M, Cuttaia HC, Palazzo D, Mazara MV, Lauricella SA, Malacarne M, Pierluigi M, Cavani S, Piccione M.

Ital J Pediatr. 2017 Jul 19;43(1):61. doi: 10.1186/s13052-017-0380-x.

12.

The Diagnostic Challenge of Dipyridamole-atropine Stress Echocardiography in a Patient with Myocardial Bridge.

Piccione MC, Zito C, Trio O, Oteri A, D'Angelo M, Andò G.

J Cardiovasc Echogr. 2016 Oct-Dec;26(4):120-122. doi: 10.4103/2211-4122.192175.

13.

Whole-body magnetic resonance imaging in the diagnosis and follow-up of multicentric infantile myofibromatosis: A case report.

Salerno S, Terranova MC, Rossello M, Piccione M, Ziino O, Re GL.

Mol Clin Oncol. 2017 Apr;6(4):579-582. doi: 10.3892/mco.2017.1171. Epub 2017 Feb 17.

14.

Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform.

Calì F, Chiavetta V, Ruggeri G, Piccione M, Selicorni A, Palazzo D, Bonsignore M, Cereda A, Elia M, Failla P, Figura MG, Fiumara A, Maitz S, Luana Mandarà GM, Mattina T, Ragalmuto A, Romano C, Ruggieri M, Salluzzo R, Saporoso A, Schepis C, Sorge G, Spanò M, Tortorella G, Romano V.

Eur J Med Genet. 2017 Feb;60(2):93-99. doi: 10.1016/j.ejmg.2016.11.001. Epub 2016 Nov 9.

PMID:
27838393
15.

Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients.

Zollino M, Marangi G, Ponzi E, Orteschi D, Ricciardi S, Lattante S, Murdolo M, Battaglia D, Contaldo I, Mercuri E, Stefanini MC, Caumes R, Edery P, Rossi M, Piccione M, Corsello G, Della Monica M, Scarano F, Priolo M, Gentile M, Zampino G, Vijzelaar R, Abdulrahman O, Rauch A, Oneda B, Deardorff MA, Saitta SC, Falk MJ, Dubbs H, Zackai E.

J Med Genet. 2015 Dec;52(12):804-14. doi: 10.1136/jmedgenet-2015-103184. Epub 2015 Sep 30.

PMID:
26424144
16.

Isolated double orifice mitral valve in a young asymptomatic woman.

Pizzino F, Piccione MC, Trio O, Zito C, Monaco M, Carerj S.

J Cardiovasc Med (Hagerstown). 2016 Dec;17 Suppl 2:e161-e163. doi: 10.2459/JCM.0000000000000308.

PMID:
26204470
17.

2p15-p16.1 microdeletions encompassing and proximal to BCL11A are associated with elevated HbF in addition to neurologic impairment.

Funnell AP, Prontera P, Ottaviani V, Piccione M, Giambona A, Maggio A, Ciaffoni F, Stehling-Sun S, Marra M, Masiello F, Varricchio L, Stamatoyannopoulos JA, Migliaccio AR, Papayannopoulou T.

Blood. 2015 Jul 2;126(1):89-93. doi: 10.1182/blood-2015-04-638528. Epub 2015 May 27.

18.

Oral peptide specific egg antibody to intestinal sodium-dependent phosphate co-transporter-2b is effective at altering phosphate transport in vitro and in vivo.

Bobeck EA, Hellestad EM, Sand JM, Piccione ML, Bishop JW, Helvig C, Petkovich M, Cook ME.

Poult Sci. 2015 Jun;94(6):1128-37. doi: 10.3382/ps/pev085. Epub 2015 Mar 29.

19.

Multimodalities Imaging in Diagnosis of Pericardial Cyst.

Meschisi M, Piccione MC, Bella GD, Zito C.

J Cardiovasc Echogr. 2015 Apr-Jun;25(2):60-62. doi: 10.4103/2211-4122.161782.

20.

Characterization of 14 novel deletions underlying Rubinstein-Taybi syndrome: an update of the CREBBP deletion repertoire.

Rusconi D, Negri G, Colapietro P, Picinelli C, Milani D, Spena S, Magnani C, Silengo MC, Sorasio L, Curtisova V, Cavaliere ML, Prontera P, Stangoni G, Ferrero GB, Biamino E, Fischetto R, Piccione M, Gasparini P, Salviati L, Selicorni A, Finelli P, Larizza L, Gervasini C.

Hum Genet. 2015 Jun;134(6):613-26. doi: 10.1007/s00439-015-1542-9. Epub 2015 Mar 25.

PMID:
25805166
21.

4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterization.

Piccione M, Salzano E, Vecchio D, Ferrara D, Malacarne M, Pierluigi M, Ferrara I, Corsello G.

Eur J Paediatr Neurol. 2015 Jul;19(4):477-83. doi: 10.1016/j.ejpn.2015.02.002. Epub 2015 Feb 23.

PMID:
25769226
22.

Left atrial function in cardiac amyloidosis.

Di Bella G, Minutoli F, Madaffari A, Mazzeo A, Russo M, Donato R, Zito C, Aquaro GD, Piccione MC, Pedri S, Vita G, Pingitore A, Carerj S.

J Cardiovasc Med (Hagerstown). 2016 Feb;17(2):113-21. doi: 10.2459/JCM.0000000000000188.

PMID:
25222078
23.

Intrauterine growth pattern and birthweight discordance in twin pregnancies: a retrospective study.

Puccio G, Giuffré M, Piccione M, Piro E, Malerba V, Corsello G.

Ital J Pediatr. 2014 May 5;40:43. doi: 10.1186/1824-7288-40-43.

24.

Response to Stanich et al.: Correspondence regarding-PTEN hamartoma tumor syndromes in childhood-Description of two cases and a proposal for follow-up protocol.

Piccione M, Fragapane T, Antona V, Giachino D, Cupido F, Corsello G.

Am J Med Genet A. 2014 Jul;164A(7):1871. doi: 10.1002/ajmg.a.36527. Epub 2014 Apr 3. No abstract available.

PMID:
24700784
25.

[Molecular aspects of the antiviral response against hepatitis C virus implicated in vaccines development].

Llanes MS, Palacios NS, Piccione M, Ruiz MG, Layana C.

Enferm Infecc Microbiol Clin. 2015 Apr;33(4):273-80. doi: 10.1016/j.eimc.2013.12.012. Epub 2014 Feb 14. Review. Spanish.

PMID:
24529681
26.

Variable phenotype in 17q12 microdeletions: clinical and molecular characterization of a new case.

Palumbo P, Antona V, Palumbo O, Piccione M, Nardello R, Fontana A, Carella M, Corsello G.

Gene. 2014 Apr 1;538(2):373-8. doi: 10.1016/j.gene.2014.01.050. Epub 2014 Jan 29.

PMID:
24487052
27.

PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol.

Piccione M, Fragapane T, Antona V, Giachino D, Cupido F, Corsello G.

Am J Med Genet A. 2013 Nov;161A(11):2902-8. doi: 10.1002/ajmg.a.36266. Epub 2013 Oct 7.

PMID:
24123798
28.

Delineating a new critical region for juvenile myoclonic epilepsy at the 22q11.2 chromosome.

Piccione M, Vecchio D, Salzano E, Corsello G.

Epilepsy Behav. 2013 Dec;29(3):587-8. doi: 10.1016/j.yebeh.2013.08.008. Epub 2013 Sep 5. No abstract available.

PMID:
24012507
29.

Newborn screening of inherited metabolic disorders by tandem mass spectrometry: past, present and future.

Scaturro G, Sanfilippo C, Piccione M, Piro E, Giuffrè M, Corsello G.

Pediatr Med Chir. 2013 May-Jun;35(3):105-9.

PMID:
23947109
30.

Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?

La Placa S, Giuffrè M, Gangemi A, Di Noto S, Matina F, Nociforo F, Antona V, Di Pace MR, Piccione M, Corsello G.

Ital J Pediatr. 2013 Jul 10;39:45. doi: 10.1186/1824-7288-39-45.

31.

Role of imaging in assessment of atrial fibrosis in patients with atrial fibrillation: state-of-the-art review.

Longobardo L, Todaro MC, Zito C, Piccione MC, Di Bella G, Oreto L, Khandheria BK, Carerj S.

Eur Heart J Cardiovasc Imaging. 2014 Jan;15(1):1-5. doi: 10.1093/ehjci/jet116. Epub 2013 Jun 24. Review.

PMID:
23798579
32.

Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral artery.

Piro E, Piccione M, Marrone G, Giuffrè M, Corsello G.

Ital J Pediatr. 2013 May 14;39:32. doi: 10.1186/1824-7288-39-32.

33.

Intrauterine growth restriction and congenital malformations: a retrospective epidemiological study.

Puccio G, Giuffré M, Piccione M, Piro E, Rinaudo G, Corsello G.

Ital J Pediatr. 2013 Apr 11;39:23. doi: 10.1186/1824-7288-39-23.

34.

Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas.

Isidor B, Bourdeaut F, Lafon D, Plessis G, Lacaze E, Kannengiesser C, Rossignol S, Pichon O, Briand A, Martin-Coignard D, Piccione M, David A, Delattre O, Jeanpierre C, Sévenet N, Le Caignec C.

Eur J Hum Genet. 2013 Jul;21(7):784-7. doi: 10.1038/ejhg.2012.252. Epub 2012 Nov 21.

35.

Images in cardiovascular medicine: caseous calcification of the mitral annulus.

Pugliatti P, Piccione MC, Ascenti G, Germanò A, Recupero A, Oreto G, Carerj S.

Echocardiography. 2013 Feb;30(2):E30-2. doi: 10.1111/echo.12033. Epub 2012 Nov 21.

PMID:
23167713
36.

[Motivation in brief psychotherapy: a 30 patients study, valued in a psychiatric day-hospital].

Spanò L, Rusconi AC, Piccione M, Coccanari de' Fornari MA.

Riv Psichiatr. 2012 Nov-Dec;47(6):508-14. doi: 10.1708/1178.13057. Italian.

PMID:
23160111
37.

14q13.1-21.1 deletion encompassing the HPE8 locus in an adolescent with intellectual disability and bilateral microphthalmia, but without holoprosencephaly.

Piccione M, Serra G, Consiglio V, Di Fiore A, Cavani S, Grasso M, Malacarne M, Pierluigi M, Viaggi C, Corsello G.

Am J Med Genet A. 2012 Jun;158A(6):1427-33. doi: 10.1002/ajmg.a.35334. Epub 2012 May 11.

PMID:
22581785
38.

Characterization of a complex rearrangement involving chromosomes 1, 4 and 8 by FISH and array-CGH.

Viaggi CD, Cavani S, Pierluigi M, Antona V, Piro E, Corsello G, Mogni M, Piccione M, Malacarne M.

J Appl Genet. 2012 Aug;53(3):285-8. doi: 10.1007/s13353-012-0097-x. Epub 2012 Apr 29.

PMID:
22544656
39.

Maternally-derived antibody to fibroblast growth factor-23 reduced dietary phosphate requirements in growing chicks.

Bobeck EA, Burgess KS, Jarmes TR, Piccione ML, Cook ME.

Biochem Biophys Res Commun. 2012 Apr 13;420(3):666-70. doi: 10.1016/j.bbrc.2012.03.063. Epub 2012 Mar 17.

PMID:
22450330
40.

Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlation.

Piccione M, Piro E, Serraino F, Cavani S, Ciccone R, Malacarne M, Pierluigi M, Vitaloni M, Zuffardi O, Corsello G.

Eur J Med Genet. 2012 Apr;55(4):238-44. doi: 10.1016/j.ejmg.2012.01.014. Epub 2012 Feb 18.

PMID:
22406401
41.

A new mutation in EDA gene in X-linked hypohidrotic ectodermal dysplasia associated with keratoconus.

Piccione M, Serra G, Sanfilippo C, Andreucci E, Sani I, Corsello G.

Minerva Pediatr. 2012 Feb;64(1):59-64.

PMID:
22350046
42.

Molecular and clinical characterization of a small duplication Xp in a human female with psychiatric disorders.

Piccione M, Sanfilippo C, Cavani S, Salatiello P, Malacarne M, Pierluigi M, Fichera M, Luciano D, Corsello G.

J Genet. 2011 Dec;90(3):473-7. No abstract available.

43.

Array-CGH and clinical characterization in a patient with subtelomeric 6p deletion without ocular dysgenesis.

Piccione M, Antona R, Salzano E, Cavani S, Malacarne M, Morreale Bubella R, Pierluigi M, Viaggi CD, Corsello G.

Am J Med Genet A. 2012 Jan;158A(1):150-4. doi: 10.1002/ajmg.a.34308. Epub 2011 Nov 21.

PMID:
22105932
44.

Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.

Striano P, Coppola A, Paravidino R, Malacarne M, Gimelli S, Robbiano A, Traverso M, Pezzella M, Belcastro V, Bianchi A, Elia M, Falace A, Gazzerro E, Ferlazzo E, Freri E, Galasso R, Gobbi G, Molinatto C, Cavani S, Zuffardi O, Striano S, Ferrero GB, Silengo M, Cavaliere ML, Benelli M, Magi A, Piccione M, Dagna Bricarelli F, Coviello DA, Fichera M, Minetti C, Zara F.

Arch Neurol. 2012 Mar;69(3):322-30. doi: 10.1001/archneurol.2011.1999. Epub 2011 Nov 14. Review.

45.

The first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplication.

Piccione M, Vecchio D, Cavani S, Malacarne M, Pierluigi M, Corsello G.

Am J Med Genet A. 2011 Dec;155A(12):3054-9. doi: 10.1002/ajmg.a.34275. Epub 2011 Oct 14.

PMID:
22002912
46.

Histone acetylation deficits in lymphoblastoid cell lines from patients with Rubinstein-Taybi syndrome.

Lopez-Atalaya JP, Gervasini C, Mottadelli F, Spena S, Piccione M, Scarano G, Selicorni A, Barco A, Larizza L.

J Med Genet. 2012 Jan;49(1):66-74. doi: 10.1136/jmedgenet-2011-100354. Epub 2011 Oct 7.

47.

Deletion of NSD1 exon 14 in Sotos syndrome: first description.

Piccione M, Consiglio V, Di Fiore A, Grasso M, Cecconi M, Perroni L, Corsello G.

J Genet. 2011 Apr;90(1):119-23. No abstract available.

48.

Early identification of vascular damage in patients with systemic sclerosis.

Piccione MC, Bagnato G, Zito C, Di Bella G, Caliri A, Catalano M, Longordo C, Oreto G, Bagnato G, Carerj S.

Angiology. 2011 May;62(4):338-43. doi: 10.1177/0003319710387918.

PMID:
21474468
49.

[Defense mechanisms as outcome measure in short-term psychotherapy related to symptoms, severity and overall functioning: a preliminary study].

Coccanari de' Fornari MA, Piccione M, Maiello L, Giampà A.

Riv Psichiatr. 2011 Jan-Feb;46(1):44-56. Italian.

PMID:
21446111
50.

Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13C.

Gripp KW, Hopkins E, Sol-Church K, Stabley DL, Axelrad ME, Doyle D, Dobyns WB, Hudson C, Johnson J, Tenconi R, Graham GE, Sousa AB, Heller R, Piccione M, Corsello G, Herman GE, Tartaglia M, Lin AE.

Am J Med Genet A. 2011 Apr;155A(4):706-16. doi: 10.1002/ajmg.a.33884. Epub 2011 Mar 15.

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