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Items: 49

1.

For common community phylogenetic analyses, go ahead and use synthesis phylogenies.

Li D, Trotta L, Marx HE, Allen JM, Sun M, Soltis DE, Soltis PS, Guralnick RP, Baiser B.

Ecology. 2019 Jun 21:e02788. doi: 10.1002/ecy.2788. [Epub ahead of print]

PMID:
31225900
2.

Working memory in posterior cortical atrophy.

Trotta L, Lamoureux D, Bartolomeo P, Migliaccio R.

Neurol Sci. 2019 Apr 8. doi: 10.1007/s10072-019-03869-5. [Epub ahead of print]

PMID:
30963338
3.

Haploinsufficiency of A20 impairs protein-protein interactome and leads into caspase-8-dependent enhancement of NLRP3 inflammasome activation.

Rajamäki K, Keskitalo S, Seppänen M, Kuismin O, Vähäsalo P, Trotta L, Väänänen A, Glumoff V, Keskitalo P, Kaarteenaho R, Jartti A, Hautala N, Jackson P, Nordström DC, Saarela J, Hautala T, Eklund KK, Varjosalo M.

RMD Open. 2018 Oct 17;4(2):e000740. doi: 10.1136/rmdopen-2018-000740. eCollection 2018.

4.

Community phylogeny of the globally critically imperiled pine rockland ecosystem.

Trotta LB, Baiser B, Possley J, Li D, Lange J, Martin S, Sessa EB.

Am J Bot. 2018 Oct;105(10):1735-1747. doi: 10.1002/ajb2.1168. Epub 2018 Oct 9.

PMID:
30300935
5.

Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders.

Trotta L, Norberg A, Taskinen M, Béziat V, Degerman S, Wartiovaara-Kautto U, Välimaa H, Jahnukainen K, Casanova JL, Seppänen M, Saarela J, Koskenvuo M, Martelius T.

Orphanet J Rare Dis. 2018 Aug 17;13(1):139. doi: 10.1186/s13023-018-0864-9.

6.

Incidence and Clinical Features of Autoimmune Hepatitis in the Province of Santa Fe (Argentina).

Costaguta A, González A, Pochettino S, Trotta L, Vicentín R, Wagener M.

J Pediatr Gastroenterol Nutr. 2018 Dec;67(6):e107-e110. doi: 10.1097/MPG.0000000000002122.

PMID:
30095578
7.

Older People Who Are Frequent Users of Acute Care: A Symptom of Fragmented Care? A Case Series Report on Patients' Pathways of Care.

Dollard J, Harvey G, Dent E, Trotta L, Williams N, Beilby J, Hoon E, Kitson A, Seiboth C, Karnon J.

J Frailty Aging. 2018;7(3):193-195. doi: 10.14283/10.14283/jfa.2018.12.

PMID:
30095151
8.

Community assembly of the ferns of Florida.

Sessa EB, Chambers SM, Li D, Trotta L, Endara L, Burleigh JG, Baiser B.

Am J Bot. 2018 Mar;105(3):549-564. doi: 10.1002/ajb2.1073. Epub 2018 May 5.

9.

ADA2 deficiency: Clonal lymphoproliferation in a subset of patients.

Trotta L, Martelius T, Siitonen T, Hautala T, Hämäläinen S, Juntti H, Taskinen M, Ilander M, Andersson EI, Zavialov A, Kaustio M, Keski-Filppula R, Hershfield M, Mustjoki S, Tapiainen T, Seppänen M, Saarela J.

J Allergy Clin Immunol. 2018 Apr;141(4):1534-1537.e8. doi: 10.1016/j.jaci.2018.01.012. Epub 2018 Jan 31. No abstract available.

PMID:
29391253
10.

Peripheral T-Cell Reactivity to Heat Shock Protein 70 and Its Cofactor GrpE from Tropheryma whipplei Is Reduced in Patients with Classical Whipple's Disease.

Trotta L, Weigt K, Schinnerling K, Geelhaar-Karsch A, Oelkers G, Biagi F, Corazza GR, Allers K, Schneider T, Erben U, Moos V.

Infect Immun. 2017 Jul 19;85(8). pii: e00363-17. doi: 10.1128/IAI.00363-17. Print 2017 Aug.

11.

Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes.

Kaustio M, Haapaniemi E, Göös H, Hautala T, Park G, Syrjänen J, Einarsdottir E, Sahu B, Kilpinen S, Rounioja S, Fogarty CL, Glumoff V, Kulmala P, Katayama S, Tamene F, Trotta L, Morgunova E, Krjutškov K, Nurmi K, Eklund K, Lagerstedt A, Helminen M, Martelius T, Mustjoki S, Taipale J, Saarela J, Kere J, Varjosalo M, Seppänen M.

J Allergy Clin Immunol. 2017 Sep;140(3):782-796. doi: 10.1016/j.jaci.2016.10.054. Epub 2017 Jan 21.

PMID:
28115215
12.

International consensus conference on open abdomen in trauma.

Chiara O, Cimbanassi S, Biffl W, Leppaniemi A, Henry S, Scalea TM, Catena F, Ansaloni L, Chieregato A, de Blasio E, Gambale G, Gordini G, Nardi G, Paldalino P, Gossetti F, Dionigi P, Noschese G, Tugnoli G, Ribaldi S, Sgardello S, Magnone S, Rausei S, Mariani A, Mengoli F, di Saverio S, Castriconi M, Coccolini F, Negreanu J, Razzi S, Coniglio C, Morelli F, Buonanno M, Lippi M, Trotta L, Volpi A, Fattori L, Zago M, de Rai P, Sammartano F, Manfredi R, Cingolani E.

J Trauma Acute Care Surg. 2016 Jan;80(1):173-83. doi: 10.1097/TA.0000000000000882. Review.

PMID:
27551925
13.

Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland.

Trotta L, Hautala T, Hämäläinen S, Syrjänen J, Viskari H, Almusa H, Lepisto M, Kaustio M, Porkka K, Palotie A, Seppänen M, Saarela J.

Eur J Hum Genet. 2016 Oct;24(10):1473-8. doi: 10.1038/ejhg.2016.37. Epub 2016 May 4.

14.

Functional Connectivity of Ventral and Dorsal Visual Streams in Posterior Cortical Atrophy.

Migliaccio R, Gallea C, Kas A, Perlbarg V, Samri D, Trotta L, Michon A, Lacomblez L, Dubois B, Lehericy S, Bartolomeo P.

J Alzheimers Dis. 2016;51(4):1119-30. doi: 10.3233/JAD-150934.

PMID:
26923019
15.

-295 T-to-C promoter region IL-16 gene polymorphism is associated with Whipple's disease.

Biagi F, Schiepatti A, Badulli C, Sbarsi I, Trotta L, Feurle GE, Müller C, Moos V, Schneider T, Marth T, De Amici M, Martinetti M, Corazza GR.

Eur J Clin Microbiol Infect Dis. 2015 Sep;34(9):1919-21. doi: 10.1007/s10096-015-2433-7. Epub 2015 Jul 8.

PMID:
26154181
16.

Alpha and beta EEG power reflects L-dopa acute administration in parkinsonian patients.

Melgari JM, Curcio G, Mastrolilli F, Salomone G, Trotta L, Tombini M, di Biase L, Scrascia F, Fini R, Fabrizio E, Rossini PM, Vernieri F.

Front Aging Neurosci. 2014 Nov 5;6:302. doi: 10.3389/fnagi.2014.00302. eCollection 2014.

17.

Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3.

Haapaniemi EM, Kaustio M, Rajala HL, van Adrichem AJ, Kainulainen L, Glumoff V, Doffinger R, Kuusanmäki H, Heiskanen-Kosma T, Trotta L, Chiang S, Kulmala P, Eldfors S, Katainen R, Siitonen S, Karjalainen-Lindsberg ML, Kovanen PE, Otonkoski T, Porkka K, Heiskanen K, Hänninen A, Bryceson YT, Uusitalo-Seppälä R, Saarela J, Seppänen M, Mustjoki S, Kere J.

Blood. 2015 Jan 22;125(4):639-48. doi: 10.1182/blood-2014-04-570101. Epub 2014 Oct 27.

18.

Relationship among diffusion tensor imaging, EEG activity, and cognitive status in mild cognitive impairment and Alzheimer's disease patients.

Scrascia F, Curcio G, Ursini F, Trotta L, Quintiliani L, Migliore S, Altamura C, Pitocco F, Altavilla R, Melgari JM, Quattrocchi CC, Vernieri F.

J Alzheimers Dis. 2014;38(4):939-50. doi: 10.3233/JAD-130788.

PMID:
24121958
19.

Magneto immunofluorescence assay for diagnosis of celiac disease.

Kergaravat SV, Beltramino L, Garnero N, Trotta L, Wagener M, Fabiano SN, Pividori MI, Hernandez SR.

Anal Chim Acta. 2013 Oct 10;798:89-96. doi: 10.1016/j.aca.2013.09.009. Epub 2013 Sep 10.

PMID:
24070488
20.

Intronic rs2147363 variant in ATP7B transcription factor-binding site associated with Alzheimer's disease.

Bucossi S, Polimanti R, Ventriglia M, Mariani S, Siotto M, Ursini F, Trotta L, Scrascia F, Callea A, Vernieri F, Squitti R.

J Alzheimers Dis. 2013;37(2):453-9. doi: 10.3233/JAD-130431.

PMID:
23948886
21.

ATP7B variants as modulators of copper dyshomeostasis in Alzheimer's disease.

Squitti R, Polimanti R, Siotto M, Bucossi S, Ventriglia M, Mariani S, Vernieri F, Scrascia F, Trotta L, Rossini PM.

Neuromolecular Med. 2013 Sep;15(3):515-22. doi: 10.1007/s12017-013-8237-y. Epub 2013 Jun 13.

PMID:
23760784
22.

Electrochemical magneto immunosensor for the detection of anti-TG2 antibody in celiac disease.

Kergaravat SV, Beltramino L, Garnero N, Trotta L, Wagener M, Isabel Pividori M, Hernandez SR.

Biosens Bioelectron. 2013 Oct 15;48:203-9. doi: 10.1016/j.bios.2013.04.012. Epub 2013 Apr 17.

PMID:
23685317
23.

Dental enamel defects in adult coeliac disease: prevalence and correlation with symptoms and age at diagnosis.

Trotta L, Biagi F, Bianchi PI, Marchese A, Vattiato C, Balduzzi D, Collesano V, Corazza GR.

Eur J Intern Med. 2013 Dec;24(8):832-4. doi: 10.1016/j.ejim.2013.03.007. Epub 2013 Apr 6.

PMID:
23571066
24.

Prevalence and natural history of potential celiac disease in adult patients.

Biagi F, Trotta L, Alfano C, Balduzzi D, Staffieri V, Bianchi PI, Marchese A, Vattiato C, Zilli A, Luinetti O, Gobbi P, Corazza GR.

Scand J Gastroenterol. 2013 May;48(5):537-42. doi: 10.3109/00365521.2013.777470. Epub 2013 Mar 19.

PMID:
23506211
25.

Quality of life in coeliac patients: Italian validation of a coeliac questionnaire.

Marchese A, Klersy C, Biagi F, Balduzzi D, Bianchi PI, Trotta L, Vattiato C, Zilli A, Rademacher J, Andrealli A, Astegiano M, Michelini I, Häuser W, Corazza GR.

Eur J Intern Med. 2013 Jan;24(1):87-91. doi: 10.1016/j.ejim.2012.09.015. Epub 2012 Oct 25.

PMID:
23102568
26.

Whipple's disease.

Biagi F, Trotta L, Corazza GR.

Intern Emerg Med. 2012 Oct;7 Suppl 3:S209-13. doi: 10.1007/s11739-012-0801-1. Review.

PMID:
23073859
27.

Cytokine genetic profile in Whipple's disease.

Biagi F, Badulli C, Feurle GE, Müller C, Moos V, Schneider T, Marth T, Mytilineos J, Garlaschelli F, Marchese A, Trotta L, Bianchi PI, Di Stefano M, Cremaschi AL, De Silvestri A, Salvaneschi L, Martinetti M, Corazza GR.

Eur J Clin Microbiol Infect Dis. 2012 Nov;31(11):3145-50. doi: 10.1007/s10096-012-1677-8. Epub 2012 Jul 31.

PMID:
22847580
28.

Previous immunosuppressive therapy is a risk factor for immune reconstitution inflammatory syndrome in Whipple's disease.

Biagi F, Trotta L, Di Stefano M, Balduzzi D, Marchese A, Vattiato C, Bianchi PI, Fenollar F, Corazza GR.

Dig Liver Dis. 2012 Oct;44(10):880-2. doi: 10.1016/j.dld.2012.05.008. Epub 2012 Jun 15.

PMID:
22704397
29.

Relationship between previous treatments and onset of symptoms in patients with Whipple's disease.

Trotta L, Biagi F, Di Stefano M, Corazza GR.

Intern Emerg Med. 2014 Mar;9(2):161-4. doi: 10.1007/s11739-012-0799-4. Epub 2012 Jun 14.

PMID:
22696297
30.

Global analysis of dynamical decision-making models through local computation around the hidden saddle.

Trotta L, Bullinger E, Sepulchre R.

PLoS One. 2012;7(3):e33110. doi: 10.1371/journal.pone.0033110. Epub 2012 Mar 15.

31.

A score that verifies adherence to a gluten-free diet: a cross-sectional, multicentre validation in real clinical life.

Biagi F, Bianchi PI, Marchese A, Trotta L, Vattiato C, Balduzzi D, Brusco G, Andrealli A, Cisarò F, Astegiano M, Pellegrino S, Magazzù G, Klersy C, Corazza GR.

Br J Nutr. 2012 Nov 28;108(10):1884-8. doi: 10.1017/S0007114511007367. Epub 2012 Feb 10.

PMID:
22321199
32.

SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population.

Trotta L, Guella I, Soldà G, Sironi F, Tesei S, Canesi M, Pezzoli G, Goldwurm S, Duga S, Asselta R.

Parkinsonism Relat Disord. 2012 Mar;18(3):257-62. doi: 10.1016/j.parkreldis.2011.10.014. Epub 2011 Nov 21.

33.

An unusual cause of dementia: essential diagnostic elements of corticobasal degeneration-a case report and review of the literature.

Mastrolilli F, Benvenga A, Di Biase L, Giambattistelli F, Trotta L, Salomone G, Quintiliani L, Landi D, Melgari JM, Vernieri F.

Int J Alzheimers Dis. 2011;2011:536141. doi: 10.4061/2011/536141. Epub 2011 Jul 12.

34.

Transcranial magnetic stimulation studies in Alzheimer's disease.

Guerra A, Assenza F, Bressi F, Scrascia F, Del Duca M, Ursini F, Vollaro S, Trotta L, Tombini M, Chisari C, Ferreri F.

Int J Alzheimers Dis. 2011;2011:263817. doi: 10.4061/2011/263817. Epub 2011 Jul 6.

35.

Influence of HLA-DQ2 and DQ8 on severity in celiac Disease.

Biagi F, Bianchi PI, Vattiato C, Marchese A, Trotta L, Badulli C, De Silvestri A, Martinetti M, Corazza GR.

J Clin Gastroenterol. 2012 Jan;46(1):46-50. doi: 10.1097/MCG.0b013e318221077e.

PMID:
21694611
36.

GJB2 and MTRNR1 contributions in children with hearing impairment from Northern Cameroon.

Trotta L, Iacona E, Primignani P, Castorina P, Radaelli C, Del Bo L, Coviello D, Ambrosetti U.

Int J Audiol. 2011 Feb;50(2):133-8. doi: 10.3109/14992027.2010.537377. Epub 2010 Nov 29.

PMID:
21114417
37.

Molecular characterization of paediatric idiopathic hypereosinophilia.

Rapanotti MC, Caruso R, Ammatuna E, Zaza S, Trotta L, Divona M, Cicconi L, Funaro D, Federici G, Amadori S, De Rossi G, Lo-Coco F.

Br J Haematol. 2010 Dec;151(5):440-6. doi: 10.1111/j.1365-2141.2010.08394.x. Epub 2010 Oct 19.

PMID:
20955401
38.

Cortical neuromodulation modifies cerebral vasomotor reactivity.

Vernieri F, Assenza G, Maggio P, Tibuzzi F, Zappasodi F, Altamura C, Corbetto M, Trotta L, Palazzo P, Ercolani M, Tecchio F, Rossini PM.

Stroke. 2010 Sep;41(9):2087-90. doi: 10.1161/STROKEAHA.110.583088. Epub 2010 Jul 29.

PMID:
20671257
39.

Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene.

Guella I, Pistocchi A, Asselta R, Rimoldi V, Ghilardi A, Sironi F, Trotta L, Primignani P, Zini M, Zecchinelli A, Coviello D, Pezzoli G, Del Giacco L, Duga S, Goldwurm S.

Neurobiol Aging. 2011 Nov;32(11):1994-2005. doi: 10.1016/j.neurobiolaging.2009.12.016. Epub 2010 Jan 8.

PMID:
20060621
40.

Anti-goblet cell antibodies for the diagnosis of autoimmune enteropathy?

Biagi F, Bianchi PI, Trotta L, Corazza GR.

Am J Gastroenterol. 2009 Dec;104(12):3112. doi: 10.1038/ajg.2009.511. No abstract available.

PMID:
19956142
41.

alpha-Synuclein multiplication analysis in Italian familial Parkinson disease.

Sironi F, Trotta L, Antonini A, Zini M, Ciccone R, Della Mina E, Meucci N, Sacilotto G, Primignani P, Brambilla T, Coviello DA, Pezzoli G, Goldwurm S.

Parkinsonism Relat Disord. 2010 Mar;16(3):228-31. doi: 10.1016/j.parkreldis.2009.09.008. Epub 2009 Oct 14.

PMID:
19833540
42.

Analysis of the GJB2 and GJB6 genes in Italian patients with nonsyndromic hearing loss: frequencies, novel mutations, genotypes, and degree of hearing loss.

Primignani P, Trotta L, Castorina P, Lalatta F, Sironi F, Radaelli C, Degiorgio D, Curcio C, Travi M, Ambrosetti U, Cesarani A, Garavelli L, Formigoni P, Milani D, Murri A, Cuda D, Coviello DA.

Genet Test Mol Biomarkers. 2009 Apr;13(2):209-17. doi: 10.1089/gtmb.2008.0086.

PMID:
19371219
43.

The HLA alleles DRB1*13 and DQB1*06 are associated to Whipple's disease.

Martinetti M, Biagi F, Badulli C, Feurle GE, Müller C, Moos V, Schneider T, Marth T, Marchese A, Trotta L, Sachetto S, Pasi A, De Silvestri A, Salvaneschi L, Corazza GR.

Gastroenterology. 2009 Jun;136(7):2289-94. doi: 10.1053/j.gastro.2009.01.051. Epub 2009 Jan 27.

PMID:
19208355
44.

Well vulnerability: a quantitative approach for source water protection.

Trotta L.

Ground Water. 2007 Sep-Oct;45(5):529; author reply 530. No abstract available.

PMID:
17760578
45.

A new de novo missense mutation in connexin 26 in a sporadic case of nonsyndromic deafness.

Primignani P, Trotta L, Castorina P, Lalatta F, Cuda D, Murri A, Ambrosetti U, Cesarani A, Curcio C, Coviello D, Travi M.

Laryngoscope. 2007 May;117(5):821-4.

PMID:
17473676
46.

Multi-criteria decision making--an approach to setting priorities in health care.

Nobre FF, Trotta LT, Gomes LF.

Stat Med. 1999 Dec 15;18(23):3345-54.

PMID:
10602156
47.

Corneal topography of spontaneous perforation of acute hydrops in keratoconus.

Nicoli C, Wainsztein RD, Trotta LP.

J Cataract Refract Surg. 1999 Jun;25(6):871-2.

PMID:
10374172
48.

[Screening of urinary tract infections in schoolchildren in the area covered by the Azzate Area Health Consortium].

Bono A, Comeri G, Trotta L, Gianneo E, Marnini P, Roggia A.

Minerva Urol. 1979 Jan-Mar;31(1):67-72. Italian. No abstract available.

PMID:
470901
49.

[Epidemiology and prevention of urinary tract infections in childhood].

Trotta L, Comeri G, Marnini P.

Minerva Urol. 1978 Apr-Jun;30(2):79-84. Italian. No abstract available.

PMID:
703730

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