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Items: 1 to 50 of 205

1.

Androgen insensitivity syndrome.

Gulía C, Baldassarra S, Zangari A, Briganti V, Gigli S, Gaffi M, Signore F, Vallone C, Nucciotti R, Costantini FM, Pizzuti A, Bernardo S, Porrello A, Piergentili R.

Eur Rev Med Pharmacol Sci. 2018 Jun;22(12):3873-3887. doi: 10.26355/eurrev_201806_15272.

PMID:
29949163
2.

Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies.

Barbato E, Traversa A, Guarnieri R, Giovannetti A, Genovesi ML, Magliozzi MR, Paolacci S, Ciolfi A, Pizzi S, Di Giorgio R, Tartaglia M, Pizzuti A, Caputo V.

Arch Oral Biol. 2018 Jul;91:96-102. doi: 10.1016/j.archoralbio.2018.04.011. Epub 2018 Apr 21.

PMID:
29705498
3.

Social Workers and Mobile Child Crisis Screening.

Gilliatt A, Powell K, Pizzuti A, Arfken CL.

Health Soc Work. 2018 Feb 1;43(1):59-62. doi: 10.1093/hsw/hlx042. No abstract available.

PMID:
29190342
4.

MRI and US in the evaluation of fetal anomalies: The need to work together.

Bernardo S, Giancotti A, Antonelli A, Rizzo G, Vinci V, Pizzuti A, Catalano C, Manganaro L.

Prenat Diagn. 2017 Dec;37(13):1343-1349. doi: 10.1002/pd.5181.

PMID:
29119613
5.

Pharmacological targeting of the ephrin receptor kinase signalling by GLPG1790 in vitro and in vivo reverts oncophenotype, induces myogenic differentiation and radiosensitizes embryonal rhabdomyosarcoma cells.

Megiorni F, Gravina GL, Camero S, Ceccarelli S, Del Fattore A, Desiderio V, Papaccio F, McDowell HP, Shukla R, Pizzuti A, Beirinckx F, Pujuguet P, Saniere L, der Aar EV, Maggio R, De Felice F, Marchese C, Dominici C, Tombolini V, Festuccia C, Marampon F.

J Hematol Oncol. 2017 Oct 6;10(1):161. doi: 10.1186/s13045-017-0530-z.

6.

Training for Direct Support Staff at Group Homes for People with Chronic Mental Illness.

Amirsadri A, Pizzuti A, Smith D, Duckett D, Arfken CL.

Community Ment Health J. 2018 Jan;54(1):54-57. doi: 10.1007/s10597-017-0152-5. Epub 2017 Jul 28.

PMID:
28755133
7.

Home-Based Telepsychiatry in US Urban Area.

Amirsadri A, Burns J, Pizzuti A, Arfken CL.

Case Rep Psychiatry. 2017;2017:6296423. doi: 10.1155/2017/6296423. Epub 2017 May 29.

8.

A sketch of known and novel MYCN-associated miRNA networks in neuroblastoma.

Megiorni F, Colaiacovo M, Cialfi S, McDowell HP, Guffanti A, Camero S, Felsani A, Losty PD, Pizer B, Shukla R, Cappelli C, Ferrara E, Pizzuti A, Moles A, Dominici C.

Oncol Rep. 2017 Jul;38(1):3-20. doi: 10.3892/or.2017.5701. Epub 2017 Jun 6.

9.

Lack of pathogenic mutations in SOS1 gene in phenytoin-induced gingival overgrowth patients.

Margiotti K, Pascolini G, Consoli F, Guida V, Di Bonaventura C, Giallonardo AT, Pizzuti A, De Luca A.

Arch Oral Biol. 2017 Aug;80:160-163. doi: 10.1016/j.archoralbio.2017.04.002. Epub 2017 Apr 5.

PMID:
28433619
10.

Unusual association of SCN2A epileptic encephalopathy with severe cortical dysplasia detected by prenatal MRI.

Bernardo S, Marchionni E, Prudente S, De Liso P, Spalice A, Giancotti A, Manganaro L, Pizzuti A.

Eur J Paediatr Neurol. 2017 May;21(3):587-590. doi: 10.1016/j.ejpn.2017.01.014. Epub 2017 Feb 7.

PMID:
28254201
11.

Acute Myocardial Infarction in a Patient with Two-Vessel Occlusion and a Large Lambl's Excrescence.

Pizzuti A, Parisi F, Mosso L, Cali' Quaglia F, Tomasello A.

Case Rep Cardiol. 2016;2016:8370212. Epub 2016 Nov 22.

12.

Role of fetal MRI in the evaluation of isolated and non-isolated corpus callosum dysgenesis: results of a cross-sectional study.

Manganaro L, Bernardo S, De Vito C, Antonelli A, Marchionni E, Vinci V, Saldari M, Di Meglio L, Giancotti A, Silvestri E, Catalano C, Pizzuti A.

Prenat Diagn. 2017 Mar;37(3):244-252. doi: 10.1002/pd.4990. Epub 2017 Feb 15.

PMID:
27992967
13.

An update on the metabolic syndrome's epigenomic risk.

Perricone RA, Pizzuti A.

Minerva Endocrinol. 2017 Dec;42(4):376-384. doi: 10.23736/S0391-1977.16.02573-6. Epub 2016 Oct 28.

PMID:
27792215
14.

DNMT3B in vitro knocking-down is able to reverse embryonal rhabdomyosarcoma cell phenotype through inhibition of proliferation and induction of myogenic differentiation.

Megiorni F, Camero S, Ceccarelli S, McDowell HP, Mannarino O, Marampon F, Pizer B, Shukla R, Pizzuti A, Marchese C, Clerico A, Dominici C.

Oncotarget. 2016 Nov 29;7(48):79342-79356. doi: 10.18632/oncotarget.12688.

15.

Pfeiffer syndrome: literature review of prenatal sonographic findings and genetic diagnosis.

Giancotti A, D'Ambrosio V, Marchionni E, Squarcella A, Aliberti C, La Torre R, Manganaro L, Pizzuti A; PECRAM Study Group*.

J Matern Fetal Neonatal Med. 2017 Sep;30(18):2225-2231. doi: 10.1080/14767058.2016.1243099. Epub 2016 Oct 20. Review.

PMID:
27762162
16.

Recessive Inactivating Mutations in TBCK, Encoding a Rab GTPase-Activating Protein, Cause Severe Infantile Syndromic Encephalopathy.

Chong JX, Caputo V, Phelps IG, Stella L, Worgan L, Dempsey JC, Nguyen A, Leuzzi V, Webster R, Pizzuti A, Marvin CT, Ishak GE, Ardern-Holmes S, Richmond Z; University of Washington Center for Mendelian Genomics, Bamshad MJ, Ortiz-Gonzalez XR, Tartaglia M, Chopra M, Doherty D.

Am J Hum Genet. 2016 Apr 7;98(4):772-81. doi: 10.1016/j.ajhg.2016.01.016. Epub 2016 Mar 31.

17.

Comparative Analysis of Real-Time Polymerase Chain Reaction Methods to Typing HLA-B*57:01 in HIV-1-Positive Patients.

Falasca F, Dello Russo C, Mora B, Pirazzoli A, Fantauzzi A, Navarra P, Pizzuti A, De Vito C, Antonelli G, Turriziani O.

AIDS Res Hum Retroviruses. 2016 Jul;32(7):654-7. doi: 10.1089/AID.2015.0303. Epub 2016 Feb 10.

18.

Molecular analysis of sarcomeric and non-sarcomeric genes in patients with hypertrophic cardiomyopathy.

Bottillo I, D'Angelantonio D, Caputo V, Paiardini A, Lipari M, De Bernardo C, Giannarelli D, Pizzuti A, Majore S, Castori M, Zachara E, Re F, Grammatico P.

Gene. 2016 Feb 15;577(2):227-35. doi: 10.1016/j.gene.2015.11.048. Epub 2015 Dec 2.

PMID:
26656175
19.

Absence of left atrial stunning after cardioversion of recent-onset atrial fibrillation in patients at low-stroke risk.

Antonielli E, Pizzuti A, Dogliani S, Stasi M, Bassignana A, Doronzo B.

Eur J Emerg Med. 2017 Jun;24(3):217-223. doi: 10.1097/MEJ.0000000000000333.

PMID:
26458205
20.

Crizotinib-induced antitumour activity in human alveolar rhabdomyosarcoma cells is not solely dependent on ALK and MET inhibition.

Megiorni F, McDowell HP, Camero S, Mannarino O, Ceccarelli S, Paiano M, Losty PD, Pizer B, Shukla R, Pizzuti A, Clerico A, Dominici C.

J Exp Clin Cancer Res. 2015 Oct 6;34:112. doi: 10.1186/s13046-015-0228-4.

21.

Prenatal diagnosis of proximal focal femoral deficiency: Literature review of prenatal sonographic findings.

D'Ambrosio V, Pasquali G, Squarcella A, Marcoccia E, De Filippis A, Gatto S, Camilla A, Pizzuti A, La Torre R, Giancotti A.

J Clin Ultrasound. 2016 May;44(4):252-9. doi: 10.1002/jcu.22306. Epub 2015 Sep 26. Review.

PMID:
26408260
22.

Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus.

Prudente S, Jungtrakoon P, Marucci A, Ludovico O, Buranasupkajorn P, Mazza T, Hastings T, Milano T, Morini E, Mercuri L, Bailetti D, Mendonca C, Alberico F, Basile G, Romani M, Miccinilli E, Pizzuti A, Carella M, Barbetti F, Pascarella S, Marchetti P, Trischitta V, Di Paola R, Doria A.

Am J Hum Genet. 2015 Jul 2;97(1):177-85. doi: 10.1016/j.ajhg.2015.05.011. Epub 2015 Jun 11.

23.

The use of piezosurgery in cranial surgery in children.

Ramieri V, Saponaro G, Lenzi J, Caporlingua F, Polimeni A, Silvestri A, Pizzuti A, Roggini M, Tarani L, Papoff P, Giancotti A, Castori M, Manganaro L, Cascone P; PECRAM Study Group.

J Craniofac Surg. 2015 May;26(3):840-2. doi: 10.1097/SCS.0000000000001574. Erratum in: J Craniofac Surg. 2015 Jul;26(5):e466. Piero, Cascone [corrected to Cascone, Piero].

PMID:
25974793
24.

Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome.

Kortüm F, Caputo V, Bauer CK, Stella L, Ciolfi A, Alawi M, Bocchinfuso G, Flex E, Paolacci S, Dentici ML, Grammatico P, Korenke GC, Leuzzi V, Mowat D, Nair LD, Nguyen TT, Thierry P, White SM, Dallapiccola B, Pizzuti A, Campeau PM, Tartaglia M, Kutsche K.

Nat Genet. 2015 Jun;47(6):661-7. doi: 10.1038/ng.3282. Epub 2015 Apr 27.

PMID:
25915598
25.

The emerging role of MicroRNA in schizophrenia.

Caputo V, Ciolfi A, Macri S, Pizzuti A.

CNS Neurol Disord Drug Targets. 2015;14(2):208-21. Review.

PMID:
25613509
26.

Deep Sequencing the microRNA profile in rhabdomyosarcoma reveals down-regulation of miR-378 family members.

Megiorni F, Cialfi S, McDowell HP, Felsani A, Camero S, Guffanti A, Pizer B, Clerico A, De Grazia A, Pizzuti A, Moles A, Dominici C.

BMC Cancer. 2014 Nov 25;14:880. doi: 10.1186/1471-2407-14-880.

27.

Lack of association between serotonin transporter 5-HTT gene polymorphism and endometriosis in an Italian patient population.

Megiorni F, Resta S, Yazdanian D, Cavaggioni G, Lia C, Benedetti Panici P, Pizzuti A, Porpora MG.

J Negat Results Biomed. 2014 Jun 12;13(1):12. doi: 10.1186/1477-5751-13-12.

28.

Immunogenetic investigation in vernal keratoconjunctivitis.

Zicari AM, Mora B, Lollobrigida V, Occasi F, Cesoni Marcelli A, Megiorni F, Pizzuti A, Nebbioso M, Duse M.

Pediatr Allergy Immunol. 2014 Aug;25(5):508-10. doi: 10.1111/pai.12231. Epub 2014 Jun 5. No abstract available.

PMID:
24899226
29.

Novel SMAD4 mutation causing Myhre syndrome.

Caputo V, Bocchinfuso G, Castori M, Traversa A, Pizzuti A, Stella L, Grammatico P, Tartaglia M.

Am J Med Genet A. 2014 Jul;164A(7):1835-40. doi: 10.1002/ajmg.a.36544. Epub 2014 Apr 8.

PMID:
24715504
30.

Clinical and genetic study of two patients with Zimmermann-Laband syndrome and literature review.

Castori M, Valiante M, Pascolini G, Leuzzi V, Pizzuti A, Grammatico P.

Eur J Med Genet. 2013 Oct;56(10):570-6. doi: 10.1016/j.ejmg.2013.08.004. Epub 2013 Aug 27. Review.

PMID:
23994350
31.

From Nuremberg to bioethics: an educational project for students of dentistry and dental prosthesis.

Marinozzi S, Corbellini G, Ottolenghi L, Ripari F, Pizzuti A, Pezzetti M, Gaj F.

Ann Stomatol (Roma). 2013 Mar 20;4(1):138-41. doi: 10.11138/ads.0138. Print 2013 Jan.

32.

Loss of function of the E3 ubiquitin-protein ligase UBE3B causes Kaufman oculocerebrofacial syndrome.

Flex E, Ciolfi A, Caputo V, Fodale V, Leoni C, Melis D, Bedeschi MF, Mazzanti L, Pizzuti A, Tartaglia M, Zampino G.

J Med Genet. 2013 Aug;50(8):493-9. doi: 10.1136/jmedgenet-2012-101405. Epub 2013 May 17.

33.

Elevated levels of miR-145 correlate with SMAD3 down-regulation in cystic fibrosis patients.

Megiorni F, Cialfi S, Cimino G, De Biase RV, Dominici C, Quattrucci S, Pizzuti A.

J Cyst Fibros. 2013 Dec;12(6):797-802. doi: 10.1016/j.jcf.2013.03.007. Epub 2013 Apr 28.

34.

Cytotoxic T-lymphocyte antigen 4 (CTLA4) +49AG and CT60 gene polymorphisms in Alopecia Areata: a case-control association study in the Italian population.

Megiorni F, Mora B, Maxia C, Gerardi M, Pizzuti A, Rossi A.

Arch Dermatol Res. 2013 Sep;305(7):665-70. doi: 10.1007/s00403-013-1348-3. Epub 2013 Apr 9.

PMID:
23567921
35.

Neurocognitive effects of methylphenidate on ADHD children with different DAT genotypes: a longitudinal open label trial.

Pasini A, Sinibaldi L, Paloscia C, Douzgou S, Pitzianti MB, Romeo E, Curatolo P, Pizzuti A.

Eur J Paediatr Neurol. 2013 Jul;17(4):407-14. doi: 10.1016/j.ejpn.2013.02.002. Epub 2013 Mar 28.

PMID:
23541676
36.

Single nucleotide polymorphisms in the promoter regions of Foxp3 and ICOSLG genes are associated with Alopecia areata.

Conteduca G, Rossi A, Megiorni F, Parodi A, Ferrera F, Tardito S, Battaglia F, Kalli F, Negrini S, Pizzuti A, Rizza E, Indiveri F, Fenoglio D, Filaci G.

Clin Exp Med. 2014 Feb;14(1):91-7. doi: 10.1007/s10238-012-0224-3. Epub 2012 Nov 30.

37.

HLA-DQA1 and HLA-DQB1 in Celiac disease predisposition: practical implications of the HLA molecular typing.

Megiorni F, Pizzuti A.

J Biomed Sci. 2012 Oct 11;19:88. doi: 10.1186/1423-0127-19-88. Review.

38.

TDP-43 and FUS RNA-binding proteins bind distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transcriptional fate in motoneuron-like cells.

Colombrita C, Onesto E, Megiorni F, Pizzuti A, Baralle FE, Buratti E, Silani V, Ratti A.

J Biol Chem. 2012 May 4;287(19):15635-47. doi: 10.1074/jbc.M111.333450. Epub 2012 Mar 16.

39.

Brain derived neurotrophic factor (BDNF) expression is regulated by microRNAs miR-26a and miR-26b allele-specific binding.

Caputo V, Sinibaldi L, Fiorentino A, Parisi C, Catalanotto C, Pasini A, Cogoni C, Pizzuti A.

PLoS One. 2011;6(12):e28656. doi: 10.1371/journal.pone.0028656. Epub 2011 Dec 14.

40.

Synergistic post-transcriptional regulation of the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) by miR-101 and miR-494 specific binding.

Megiorni F, Cialfi S, Dominici C, Quattrucci S, Pizzuti A.

PLoS One. 2011;6(10):e26601. doi: 10.1371/journal.pone.0026601. Epub 2011 Oct 20.

41.

Clinical Significance of MicroRNA Expression Profiles and Polymorphisms in Lung Cancer Development and Management.

Megiorni F, Pizzuti A, Frati L.

Patholog Res Int. 2011;2011:780652. doi: 10.4061/2011/780652. Epub 2011 Jul 27.

42.

Genetic association of HLA-DQB1 and HLA-DRB1 polymorphisms with alopecia areata in the Italian population.

Megiorni F, Pizzuti A, Mora B, Rizzuti A, Garelli V, Maxia C, Carlesimo M, Fotruna MC, Delle Chiaie R, Cavaggioni G, Rossi A.

Br J Dermatol. 2011 Oct;165(4):823-7. doi: 10.1111/j.1365-2133.2011.10466.x. Epub 2011 Sep 15.

PMID:
21692766
43.

Early ultrasound suspect of thanatophoric dysplasia followed by first trimester molecular diagnosis.

Giancotti A, Castori M, Spagnuolo A, Binni F, D'Ambrosio V, Pasquali G, Pizzuti A, Grammatico P.

Am J Med Genet A. 2011 Jul;155A(7):1756-8. doi: 10.1002/ajmg.a.34052. Epub 2011 Jun 10. No abstract available.

PMID:
21671381
44.

Ulerythema ophryogenes, a rare and often misdiagnosed syndrome: analysis of an idiopathic case.

Dianzani C, Pizzuti A, Gaspardini F, Bernardini L, Rizzo B, Degener AM.

Int J Immunopathol Pharmacol. 2011 Apr-Jun;24(2):523-7.

PMID:
21658329
45.

Late gadolinium enhancement on cardiac magnetic resonance and phenotypic expression in hypertrophic cardiomyopathy.

Conte MR, Bongioanni S, Chiribiri A, Leuzzi S, Lardone E, Di Donna P, Pizzuti A, Luceri S, Cesarani F, Mabritto B, Zoccai GB, Bonamini R, Gaita F.

Am Heart J. 2011 Jun;161(6):1073-7. doi: 10.1016/j.ahj.2011.03.022.

PMID:
21641353
46.

Mitochondrial disfunction as a cause of ALS.

Pizzuti A, Petrucci S.

Arch Ital Biol. 2011 Mar;149(1):113-9. doi: 10.4449/aib.v149i1.1266. Review.

PMID:
21412720
47.

Familial spinal neurofibromatosis due to a multiexonic NF1 gene deletion.

Pizzuti A, Bottillo I, Inzana F, Lanari V, Buttarelli F, Torrente I, Giallonardo AT, De Luca A, Dallapiccola B.

Neurogenetics. 2011 Aug;12(3):233-40. doi: 10.1007/s10048-011-0278-5. Epub 2011 Mar 2.

PMID:
21365283
48.

Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome.

Scioletti AP, Brancati F, Gatta V, Antonucci I, Peissel B, Pizzuti A, Mortellaro C, Tetè S, Gherlone E, Palka G, Stuppia L.

J Craniofac Surg. 2010 Sep;21(5):1654-6. doi: 10.1097/SCS.0b013e3181ef69ef.

PMID:
20856073
49.

Genetic variants in adipose triglyceride lipase influence lipid levels in familial combined hyperlipidemia.

Nanni L, Quagliarini F, Megiorni F, Montali A, Minicocci I, Campagna F, Pizzuti A, Arca M.

Atherosclerosis. 2010 Nov;213(1):206-11. doi: 10.1016/j.atherosclerosis.2010.08.055. Epub 2010 Aug 19.

PMID:
20832801
50.

Giant scrotal elephantiasis: an idiopathic case.

Dianzani C, Gaspardini F, Persichetti P, Brunetti B, Pizzuti A, Margiotti K, Degener AM.

Int J Immunopathol Pharmacol. 2010 Jan-Mar;23(1):369-72.

PMID:
20378026

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