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Items: 1 to 50 of 63

1.

A facile method for urinary phenylalanine measurement on paper-based lab-on-chip for PKU therapy monitoring.

Messina MA, Meli C, Conoci S, Petralia S.

Analyst. 2017 Dec 4;142(24):4629-4632. doi: 10.1039/c7an01115f.

PMID:
29138767
2.

Microbiological Findings in Ready-to-Eat and Precooked Food Distributed in Public Catering Halls in Cagliari Province, Italy.

Brignardello S, Sabiu R, Tedde T, Cocco E, Pitzalis G, Meli C, Cogoni MP.

Ital J Food Saf. 2014 Sep 10;3(3):1733. eCollection 2014 Aug 28.

3.

Activity of praziquantel enantiomers and main metabolites against Schistosoma mansoni.

Meister I, Ingram-Sieber K, Cowan N, Todd M, Robertson MN, Meli C, Patra M, Gasser G, Keiser J.

Antimicrob Agents Chemother. 2014 Sep;58(9):5466-72. doi: 10.1128/AAC.02741-14. Epub 2014 Jun 30.

4.

A modular attractor associative memory with patchy connectivity and weight pruning.

Meli C, Lansner A.

Network. 2013;24(4):129-50. doi: 10.3109/0954898X.2013.859323.

PMID:
24251411
5.

Load-sensitive dynamic workflow re-orchestration and optimisation for faster patient healthcare.

Meli CL, Khalil I, Tari Z.

Comput Methods Programs Biomed. 2014;113(1):1-14. doi: 10.1016/j.cmpb.2013.06.019. Epub 2013 Aug 8.

PMID:
24099624
6.

Long-term follow-up and outcome of phenylketonuria patients on sapropterin: a retrospective study.

Keil S, Anjema K, van Spronsen FJ, Lambruschini N, Burlina A, Bélanger-Quintana A, Couce ML, Feillet F, Cerone R, Lotz-Havla AS, Muntau AC, Bosch AM, Meli CA, Billette de Villemeur T, Kern I, Riva E, Giovannini M, Damaj L, Leuzzi V, Blau N.

Pediatrics. 2013 Jun;131(6):e1881-8. doi: 10.1542/peds.2012-3291. Epub 2013 May 20.

PMID:
23690520
7.

Real-time wearable telecardiology from representative signals.

Meli C, Fernandez G, Khalil I.

Conf Proc IEEE Eng Med Biol Soc. 2011;2011:4967-71. doi: 10.1109/IEMBS.2011.6091231.

PMID:
22255453
8.

ECG biometric using multilayer perceptron and radial basis function neural networks.

Mai V, Khalil I, Meli C.

Conf Proc IEEE Eng Med Biol Soc. 2011;2011:2745-8. doi: 10.1109/IEMBS.2011.6090752.

PMID:
22254909
9.

Carbamoyl phosphate synthetase 1 deficiency in Italy: clinical and genetic findings in a heterogeneous cohort.

Funghini S, Thusberg J, Spada M, Gasperini S, Parini R, Ventura L, Meli C, De Cosmo L, Sibilio M, Mooney SD, Guerrini R, Donati MA, Morrone A.

Gene. 2012 Feb 10;493(2):228-34. doi: 10.1016/j.gene.2011.11.052. Epub 2011 Dec 7.

PMID:
22173106
10.

Clinical manifestations and management of four children with Pearson syndrome.

Tumino M, Meli C, Farruggia P, La Spina M, Faraci M, Castana C, Di Raimondo V, Alfano M, Pittalà A, Lo Nigro L, Russo G, Di Cataldo A.

Am J Med Genet A. 2011 Dec;155A(12):3063-6. doi: 10.1002/ajmg.a.34288. Epub 2011 Oct 19.

PMID:
22012855
11.

Effect of a patient navigator program on the volume and quality of colonoscopy.

Lebwohl B, Neugut AI, Stavsky E, Villegas S, Meli C, Rodriguez O, Franco C, Krauskopf MS, Rosenberg R.

J Clin Gastroenterol. 2011 May-Jun;45(5):e47-53. doi: 10.1097/MCG.0b013e3181f595c3.

12.

Clonal selection of 11q CN-LOH and CBL gene mutation in a serially studied patient during MDS progression to AML.

Barresi V, Palumbo GA, Musso N, Consoli C, Capizzi C, Meli CR, Romano A, Di Raimondo F, Condorelli DF.

Leuk Res. 2010 Nov;34(11):1539-42. doi: 10.1016/j.leukres.2010.07.004. Epub 2010 Aug 1.

PMID:
20674974
13.

Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiency.

Leuzzi V, Carducci CA, Carducci CL, Pozzessere S, Burlina A, Cerone R, Concolino D, Donati MA, Fiori L, Meli C, Ponzone A, Porta F, Strisciuglio P, Antonozzi I, Blau N.

Clin Genet. 2010 Mar;77(3):249-57. doi: 10.1111/j.1399-0004.2009.01306.x. Epub 2009 Jan 3.

PMID:
20059486
14.

Evidence for genetic heterogeneity in D-2-hydroxyglutaric aciduria.

Kranendijk M, Struys EA, Gibson KM, Wickenhagen WV, Abdenur JE, Buechner J, Christensen E, de Kremer RD, Errami A, Gissen P, Gradowska W, Hobson E, Islam L, Korman SH, Kurczynski T, Maranda B, Meli C, Rizzo C, Sansaricq C, Trefz FK, Webster R, Jakobs C, Salomons GS.

Hum Mutat. 2010 Mar;31(3):279-83. doi: 10.1002/humu.21186.

PMID:
20020533
15.

First manifestation of citrullinemia type I as differential diagnosis to postpartum psychosis in the puerperal period.

Häberle J, Vilaseca MA, Meli C, Rigoldi M, Jara F, Vecchio I, Capra C, Parini R.

Eur J Obstet Gynecol Reprod Biol. 2010 Apr;149(2):228-9. doi: 10.1016/j.ejogrb.2009.11.014. Epub 2009 Dec 14. No abstract available.

PMID:
20005624
16.

Exon deletions of the phenylalanine hydroxylase gene in Italian hyperphenylalaninemics.

Cali F, Ruggeri G, Vinci M, Meli C, Carducci C, Leuzzi V, Pozzessere S, Schinocca P, Ragalmuto A, Chiavetta V, Micciche S, Romano V.

Exp Mol Med. 2010 Feb 28;42(2):81-6. doi: 10.3858/emm.2010.42.2.009.

17.

Pharmacokinetics of sapropterin in patients with phenylketonuria.

Feillet F, Clarke L, Meli C, Lipson M, Morris AA, Harmatz P, Mould DR, Green B, Dorenbaum A, Giovannini M, Foehr E; Sapropterin Research Group.

Clin Pharmacokinet. 2008;47(12):817-25. doi: 10.2165/0003088-200847120-00006.

PMID:
19026037
18.

Chromium (VI) reduction in activated sludge bacteria exposed to high chromium loading.

Molokwane PE, Meli CK, Chirwa EM.

Water Sci Technol. 2008;58(2):399-405. doi: 10.2166/wst.2008.669.

PMID:
18701792
19.

Neonatal hypophosphatasia and seizures. A case report.

Smilari P, Romeo DM, Palazzo P, Meli C, Sorge G.

Minerva Pediatr. 2005 Oct;57(5):319-23.

PMID:
16205618
20.

Maternal exposure to the antiepileptic drug vigabatrin affects postnatal development in the rat.

Lombardo SA, Leanza G, Meli C, Lombardo ME, Mazzone L, Vincenti I, Cioni M.

Neurol Sci. 2005 Jun;26(2):89-94.

PMID:
15995825
21.

Unexpectedly high prevalence of sexually transmitted diseases in married women attending family planning clinics in Yaounde, Cameroon.

Mbu RE, Mbopi-Keou FX, Alemnji G, Meli C, Eteki N, Nkengasong JN, Belec L, Leke RJ.

Int J STD AIDS. 2005 Mar;16(3):270-1. No abstract available. Erratum in: Int J STD AIDS. 2005 Sep;16(9):650. Alemdji, G [corrected to Alemnji, G].

PMID:
15829032
22.

Reduction of materno-fetal transmission of HIV by improved delivery techniques combined with nevirapine treatment in women attending two family planning clinics in Yaounde, Cameroon.

Mbu RE, Mbopi-Keou FX, Alemnji G, Nkengasong JN, Meli C, Eteki N, Nana PN, Ako SN, Tonye RN, Leke RJ.

Int J STD AIDS. 2004 Dec;15(12):848-9. No abstract available. Erratum in: Int J STD AIDS. 2005 Sep;16(9):650. Alemdji, G [corrected to Alemnji, G].

PMID:
15601503
23.

Acute promyelocytic leukemia during pregnancy: report of 3 cases.

Consoli U, Figuera A, Milone G, Meli CR, Guido G, Indelicato F, Moschetti G, Leotta S, Tornello A, Poidomani M, Murgano P, Pinto V, Giustolisi R.

Int J Hematol. 2004 Jan;79(1):31-6. Review.

PMID:
14979475
24.

Dihydropyrimidine dehydrogenase deficiency and acute neurological presentation.

Fiumara A, van Kuilenburg AB, Caruso U, Nucifora C, Marzullo E, Barone R, Meli C, van Gennip AH.

J Inherit Metab Dis. 2003;26(4):407-9.

PMID:
12971429
25.

Autism and phenylketonuria.

Baieli S, Pavone L, Meli C, Fiumara A, Coleman M.

J Autism Dev Disord. 2003 Apr;33(2):201-4.

PMID:
12757360
26.

Dietary control of phenylketonuria.

Meli C, Bianca S.

Lancet. 2002 Dec 21-28;360(9350):2075-6. No abstract available.

PMID:
12504428
27.

Hyperphenylalaninemia and birth weight.

Bianca S, Meli C, Barrano B, Mollica F.

Ann Genet. 2002 Jul-Sep;45(3):105-7.

PMID:
12381438
28.

PAH gene mutations in the Sicilian population: association with minihaplotypes and expression analysis.

Mirisola MG, Cali F, Gloria A, Schinocca P, D'Amato M, Cassara G, Leo GD, Palillo L, Meli C, Romano V.

Mol Genet Metab. 2001 Nov;74(3):353-61.

PMID:
11708866
29.

Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.

Salvi S, Santorelli FM, Bertini E, Boldrini R, Meli C, Donati A, Burlina AB, Rizzo C, Di Capua M, Fariello G, Dionisi-Vici C.

Neurology. 2001 Sep 11;57(5):911-4.

PMID:
11552031
30.

Genotype-phenotype correlation in dihydropteridine reductase deficiency.

de Sanctis L, Alliaudi C, Spada M, Farrugia R, Cerone R, Biasucci G, Meli C, Zammarchi E, Coskun T, Blau N, Ponzone A, Dianzani I.

J Inherit Metab Dis. 2000 Jun;23(4):333-7. No abstract available.

PMID:
10896287
31.

[A case of carcinoid with multiple sites in the jejunum and distal ileum].

Brozzetti S, Meli C, Polistena A, Musto F, De Toma G, Cavallaro A.

G Chir. 2000 Mar;21(3):95-8. Review. Italian.

PMID:
10810817
32.

Uterine diffuse adenomatoid tumor. Does it represent a different biological entity?

Di Stefano D, Faticanti Scucchi L, Covello R, Martinazzoli A, Meli C, Bosman C.

Gynecol Obstet Invest. 1998;46(1):68-72.

PMID:
9692348
33.

[Acute abdominal pain in emergency surgery. Clinical epidemiologic study of 450 patients].

Caterino S, Cavallini M, Meli C, Murante G, Schiffino L, Lotito S, Toncher F.

Ann Ital Chir. 1997 Nov-Dec;68(6):807-17; discussion 817-8. Italian.

PMID:
9646542
34.

A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype.

Guldberg P, Rey F, Zschocke J, Romano V, François B, Michiels L, Ullrich K, Hoffmann GF, Burgard P, Schmidt H, Meli C, Riva E, Dianzani I, Ponzone A, Rey J, Güttler F.

Am J Hum Genet. 1998 Jul;63(1):71-9. Erratum in: Am J Hum Genet 1998 Oct;63(4):1252-3.

35.

Eight new mutations of the phenylalanine hydroxylase gene in Italian patients with hyperphenylalaninemia.

Bosco P, Cali F, Meli C, Mollica F, Zammarchi E, Cerone R, Vanni C, Palillo L, Greco D, Romano V.

Hum Mutat. 1998;11(3):240-3.

PMID:
9521426
36.

[Recurrent leiomyoma of the rectum treated by endoscopic transanal microsurgery].

Zerilli M, Lotito S, Scarpini M, Mingazzini PL, Meli C, Lombardi A, Picchio M, Di Giorgio A, Flammia M.

G Chir. 1997 Aug-Sep;18(8-9):433-6. Italian.

PMID:
9471221
37.

Comparison between transrectal ultrasonography and computed tomography with rectal inflation of gas in preoperative staging of lower rectal cancer.

Osti MF, Padovan FS, Pirolli C, Sbarbati S, Tombolini V, Meli C, Enrici RM.

Eur Radiol. 1997;7(1):26-30.

PMID:
9000390
38.

[Nonpalpable lesions of the breast. A new technique of ultrasound-guided excision biopsy].

Di Giorgio A, Meli C, Canavese A, Arnone P, Alessandrina A, Barberio Corsetti F, Pallotti M, Campagna SA.

Minerva Chir. 1996 Dec;51(12):1139-43. Italian.

PMID:
9064589
39.

[Role of computerized tomography following transrectal air insufflation and hypotonization and transrectal ultrasonography in the staging of rectal tumors].

Osti MF, Scattoni Padovan F, Meli C, Pirolli C, Sbarbati S, Notarianni E, De Angelis d'Ossat M, Anaveri G.

Radiol Med. 1996 Nov;92(5):581-7. Italian.

PMID:
9036449
40.

PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian population.

Romano V, Guldberg P, Güttler F, Meli C, Mollica F, Pavone L, Giovannini M, Riva E, Biasucci G, Luotti D, Palillo L, Calí F, Ceratto N, Anello G, Bosco P.

J Inherit Metab Dis. 1996;19(1):15-24.

PMID:
8830172
41.

Evidence for an order-order transition on the Ge(111) surface near 1050 K from high-resolution helium atom scattering experiments.

Meli CA, Greene EF, Lange G, Toennies JP.

Phys Rev Lett. 1995 Mar 13;74(11):2054-2057. No abstract available.

PMID:
10057830
42.

Levels of L-asparagine in CSF after intramuscular administration of asparaginase from Erwinia in children with acute lymphoblastic leukemia.

Dibenedetto SP, Di Cataldo A, Ragusa R, Meli C, Lo Nigro L.

J Clin Oncol. 1995 Feb;13(2):339-44.

PMID:
7844595
43.

[Role of ultrasonography in emergency surgery].

Caterino S, Meli C, Capotondi C, Cavallini M, Zerilli M, Schiffino L, Murante G, Alessi G, Cavallaro A.

Ann Ital Chir. 1995 Jan-Feb;66(1):87-97; discussion 97-8. Italian.

PMID:
7668486
44.
45.

Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenylalaninemia in southern Europe.

Guldberg P, Romano V, Ceratto N, Bosco P, Ciuna M, Indelicato A, Mollica F, Meli C, Giovannini M, Riva E, et al.

Hum Mol Genet. 1993 Oct;2(10):1703-7.

PMID:
8268925
46.

[Surgical treatment of non-toxic multinodular goitre. Retrospective evaluation of a personal case series].

Bononi M, De Cesare A, Angelini M, Fierro A, Alessi G, Meli C, Benfari G.

Minerva Chir. 1993 Jun 30;48(12):689-94. Review. Italian.

PMID:
8414113
47.

Cytogenetic effects of benzimidazoles in mouse bone marrow.

Barale R, Scapoli C, Meli C, Casini D, Minunni M, Marrazzini A, Loprieno N, Barrai I.

Mutat Res. 1993 Jun;300(1):15-28.

PMID:
7683764
48.

[Ultrasound and color Doppler control of percutaneous angioplasty (PTA) of the renal artery].

Capotondi C, Meli C, Mingoli A, Allegrucci P, Salvatori FM, Risi D, Di Marzo L, Alessi G.

Arch Ital Urol Nefrol Androl. 1992 Jun;64 Suppl 2:121-4. Italian.

PMID:
1411586
49.

[Megaloblastic anemia: a unusual complication in an infant with double allergy to both cow's milk protein and soy].

Patanè R, Bottaro G, Meli C, Failla P, Cagnina M, Torrisi G, Castiglione N, Pennisi P.

Pediatr Med Chir. 1992 Jan-Feb;14(1):87-91. Italian.

PMID:
1579523
50.

Inter-laboratory ring trial of in vitro DNA repair tests using rat hepatocytes: further testing and conclusive remarks.

Puri EC, Baumeister M, Fautz R, Hechenberger CM, Hertner T, Meli C, Miltenburger HG, Schmid B, Schwegler R, Seeberg AM, et al.

Mutagenesis. 1991 Nov;6(6):471-8.

PMID:
1800894

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