Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 67

1.

Remediation of suspended solids and turbidity by improved settling tank design in a small-scale, free-standing toilet system using recycled blackwater.

Hawkins BT, Sellgren KL, Cellini E, J D Klem E, Rogers T, Lynch BJ, Piascik JR, Stoner BR.

Water Environ J. 2019 Feb;33(1):61-66. doi: 10.1111/wej.12369. Epub 2018 Sep 17.

2.

Diagnostic implications of genetic copy number variation in epilepsy plus.

Coppola A, Cellini E, Stamberger H, Saarentaus E, Cetica V, Lal D, Djémié T, Bartnik-Glaska M, Ceulemans B, Helen Cross J, Deconinck T, Masi S, Dorn T, Guerrini R, Hoffman-Zacharska D, Kooy F, Lagae L, Lench N, Lemke JR, Lucenteforte E, Madia F, Mefford HC, Morrogh D, Nuernberg P, Palotie A, Schoonjans AS, Striano P, Szczepanik E, Tostevin A, Vermeesch JR, Van Esch H, Van Paesschen W, Waters JJ, Weckhuysen S, Zara F, De Jonghe P, Sisodiya SM, Marini C; EuroEPINOMICS-RES Consortium; EpiCNV Consortium.

Epilepsia. 2019 Apr;60(4):689-706. doi: 10.1111/epi.14683. Epub 2019 Mar 13.

3.

Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity.

Cellini E, Vetro A, Conti V, Marini C, Doccini V, Clementella C, Parrini E, Giglio S, Della Monica M, Fichera M, Musumeci SA, Guerrini R.

Eur J Hum Genet. 2019 Jun;27(6):909-918. doi: 10.1038/s41431-019-0335-3. Epub 2019 Jan 25.

PMID:
30683929
4.

De novo KCNA1 variants in the PVP motif cause infantile epileptic encephalopathy and cognitive impairment similar to recurrent KCNA2 variants.

Rogers A, Golumbek P, Cellini E, Doccini V, Guerrini R, Wallgren-Pettersson C, Thuresson AC, Gurnett CA.

Am J Med Genet A. 2018 Aug;176(8):1748-1752. doi: 10.1002/ajmg.a.38840. Epub 2018 Jul 28.

PMID:
30055040
5.

Severe 5,10-methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia.

Perna A, Masciullo M, Modoni A, Cellini E, Parrini E, Ricci E, Donati AM, Silvestri G.

Eur J Neurol. 2018 Mar;25(3):602-605. doi: 10.1111/ene.13557. Epub 2018 Jan 30.

PMID:
29284203
6.

Clinical features and outcome of 6 new patients carrying de novo KCNB1 gene mutations.

Marini C, Romoli M, Parrini E, Costa C, Mei D, Mari F, Parmeggiani L, Procopio E, Metitieri T, Cellini E, Virdò S, De Vita D, Gentile M, Prontera P, Calabresi P, Guerrini R.

Neurol Genet. 2017 Dec 11;3(6):e206. doi: 10.1212/NXG.0000000000000206. eCollection 2017 Dec.

7.

Pyridoxine responsiveness in pyridox(am)ine-5-phosphate oxidase deficiency: The importance of early treatment.

Accorsi P, Cellini E, Paolantonio CD, Panzarino G, Verrotti A, Giordano L.

Clin Neurol Neurosurg. 2017 Dec;163:90-93. doi: 10.1016/j.clineuro.2017.10.019. Epub 2017 Oct 23. No abstract available.

PMID:
29080399
8.

Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects.

Marini C, Hardies K, Pisano T, May P, Weckhuysen S, Cellini E, Suls A, Mei D, Balling R, Jonghe PD, Helbig I, Garozzo D; EuroEPINOMICS consortium AR working group, Guerrini R.

Am J Med Genet A. 2017 Apr;173(4):1119-1123. doi: 10.1002/ajmg.a.38112.

PMID:
28328131
9.

Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes.

Parrini E, Marini C, Mei D, Galuppi A, Cellini E, Pucatti D, Chiti L, Rutigliano D, Bianchini C, Virdò S, De Vita D, Bigoni S, Barba C, Mari F, Montomoli M, Pisano T, Rosati A; Clinical Study Group, Guerrini R.

Hum Mutat. 2017 Feb;38(2):216-225. doi: 10.1002/humu.23149. Epub 2016 Dec 9.

PMID:
27864847
10.

The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy.

Cellini E, Vignoli A, Pisano T, Falchi M, Molinaro A, Accorsi P, Bontacchio A, Pinelli L, Giordano L, Guerrini R; FOXG1 Syndrome Study Group.

Dev Med Child Neurol. 2016 Jan;58(1):93-7. doi: 10.1111/dmcn.12894. Epub 2015 Sep 6.

11.

Recurrent drop attacks in early childhood as presenting symptom of benign hereditary chorea caused by TITF1 gene mutations.

Rosati A, Berti B, Melani F, Cellini E, Procopio E, Guerrini R.

Dev Med Child Neurol. 2015 Aug;57(8):777-9. doi: 10.1111/dmcn.12644. Epub 2014 Nov 20.

12.

Fat mass and obesity-associated gene (FTO) in eating disorders: evidence for association of the rs9939609 obesity risk allele with bulimia nervosa and anorexia nervosa.

Müller TD, Greene BH, Bellodi L, Cavallini MC, Cellini E, Di Bella D, Ehrlich S, Erzegovesi S, Estivill X, Fernández-Aranda F, Fichter M, Fleischhaker C, Scherag S, Gratacòs M, Grallert H, Herpertz-Dahlmann B, Herzog W, Illig T, Lehmkuhl U, Nacmias B, Ribasés M, Ricca V, Schäfer H, Scherag A, Sorbi S, Wichmann HE, Hebebrand J, Hinney A.

Obes Facts. 2012;5(3):408-19. doi: 10.1159/000340057. Epub 2012 Jun 27.

13.

Periventricular heterotopia with white matter abnormalities associated with 6p25 deletion.

Cellini E, Disciglio V, Novara F, Barkovich JA, Mencarelli MA, Hayek J, Renieri A, Zuffardi O, Guerrini R.

Am J Med Genet A. 2012 Jul;158A(7):1793-7. doi: 10.1002/ajmg.a.35416. Epub 2012 Jun 7. No abstract available.

PMID:
22678982
14.

Low social interactions in eating disorder patients in childhood and adulthood: a multi-centre European case control study.

Krug I, Penelo E, Fernandez-Aranda F, Anderluh M, Bellodi L, Cellini E, di Bernardo M, Granero R, Karwautz A, Nacmias B, Ricca V, Sorbi S, Tchanturia K, Wagner G, Collier D, Treasure J.

J Health Psychol. 2013 Jan;18(1):26-37. doi: 10.1177/1359105311435946. Epub 2012 Apr 5.

PMID:
22491496
15.

Meta-analysis of the association between variants in SORL1 and Alzheimer disease.

Reitz C, Cheng R, Rogaeva E, Lee JH, Tokuhiro S, Zou F, Bettens K, Sleegers K, Tan EK, Kimura R, Shibata N, Arai H, Kamboh MI, Prince JA, Maier W, Riemenschneider M, Owen M, Harold D, Hollingworth P, Cellini E, Sorbi S, Nacmias B, Takeda M, Pericak-Vance MA, Haines JL, Younkin S, Williams J, van Broeckhoven C, Farrer LA, St George-Hyslop PH, Mayeux R; Genetic and Environmental Risk in Alzheimer Disease 1 Consortium.

Arch Neurol. 2011 Jan;68(1):99-106. doi: 10.1001/archneurol.2010.346. Erratum in: Arch Neurol. 2011 Mar;68(3):293.

16.

Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene.

Guerrini R, Cellini E, Mei D, Metitieri T, Petrelli C, Pucatti D, Marini C, Zamponi N.

Epilepsia. 2010 Dec;51(12):2474-7. doi: 10.1111/j.1528-1167.2010.02790.x. Epub 2010 Nov 18.

17.

Factors of risk and maintenance for eating disorders: psychometric exploration of the cross-cultural questionnaire (CCQ) across five European countries.

Penelo E, Granero R, Krug I, Treasure J, Karwautz A, Anderluh M, Bellodi L, Cellini E, di Bernardo M, Nacmias B, Ricca V, Sorbi S, Tchanturia K, Wagner G, Collier D, Bonillo A, Fernández-Aranda F.

Clin Psychol Psychother. 2011 Nov-Dec;18(6):535-52. doi: 10.1002/cpp.728. Epub 2010 Sep 30.

PMID:
20886660
18.

Glucocorticoid receptor gene polymorphisms in Italian patients with eating disorders and obesity.

Cellini E, Castellini G, Ricca V, Bagnoli S, Tedde A, Rotella CM, Faravelli C, Sorbi S, Nacmias B.

Psychiatr Genet. 2010 Dec;20(6):282-8. doi: 10.1097/YPG.0b013e32833a2142.

PMID:
20440229
19.

Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease.

Gratacòs M, Escaramís G, Bustamante M, Saus E, Agüera Z, Bayés M, Cellini E, de Cid R, Fernández-Aranda F, Forcano L, González JR, Gorwood P, Hebebrand J, Hinney A, Mercader JM, Nacmias B, Ramoz N, Ribasés M, Ricca V, Romo L, Sorbi S, Versini A, Estivill X.

J Psychiatr Res. 2010 Oct;44(13):834-40. doi: 10.1016/j.jpsychires.2010.01.009. Epub 2010 Mar 9.

PMID:
20219210
20.

Immunoproteasome LMP2 60HH variant alters MBP epitope generation and reduces the risk to develop multiple sclerosis in Italian female population.

Mishto M, Bellavista E, Ligorio C, Textoris-Taube K, Santoro A, Giordano M, D'Alfonso S, Listì F, Nacmias B, Cellini E, Leone M, Grimaldi LM, Fenoglio C, Esposito F, Martinelli-Boneschi F, Galimberti D, Scarpini E, Seifert U, Amato MP, Caruso C, Foschini MP, Kloetzel PM, Franceschi C.

PLoS One. 2010 Feb 18;5(2):e9287. doi: 10.1371/journal.pone.0009287.

21.

Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease.

Nacmias B, Tedde A, Bagnoli S, Lucenteforte E, Cellini E, Piaceri I, Guarnieri BM, Bessi V, Bracco L, Sorbi S.

J Alzheimers Dis. 2010;20(1):37-41. doi: 10.3233/JAD-2010-1345.

PMID:
20164602
22.

Implication of sex and SORL1 variants in italian patients with Alzheimer disease.

Cellini E, Tedde A, Bagnoli S, Pradella S, Piacentini S, Sorbi S, Nacmias B.

Arch Neurol. 2009 Oct;66(10):1260-6. doi: 10.1001/archneurol.2009.101.

PMID:
19822782
23.

Membrane cholesterol enrichment prevents Aβ-induced oxidative stress in Alzheimer's fibroblasts.

Pensalfini A, Zampagni M, Liguri G, Becatti M, Evangelisti E, Fiorillo C, Bagnoli S, Cellini E, Nacmias B, Sorbi S, Cecchi C.

Neurobiol Aging. 2011 Feb;32(2):210-22. doi: 10.1016/j.neurobiolaging.2009.02.010. Epub 2009 Mar 17.

PMID:
19297055
24.

Implication of GAB2 gene polymorphism in Italian patients with Alzheimer's disease.

Nacmias B, Tedde A, Bagnoli S, Cellini E, Guarnieri BM, Piacentini S, Sorbi S.

J Alzheimers Dis. 2009;16(3):513-5. doi: 10.3233/JAD-2009-1005.

PMID:
19276544
25.

Leading the way. Interview by Amanda L Stefancyk.

Tuggey E, Cellini E, Pantazelos C.

Am J Nurs. 2009 Mar;109(3):68-9. doi: 10.1097/01.NAJ.0000346935.28488.5f.

PMID:
19240501
26.

Lack of association between TNF-alpha polymorphisms and Alzheimer's disease in an Italian cohort.

Tedde A, Putignano AL, Nacmias B, Bagnoli S, Cellini E, Sorbi S.

Neurosci Lett. 2008 Dec 3;446(2-3):139-42. doi: 10.1016/j.neulet.2008.09.044.

PMID:
18834925
27.

Associations of individual and family eating patterns during childhood and early adolescence: a multicentre European study of associated eating disorder factors.

Krug I, Treasure J, Anderluh M, Bellodi L, Cellini E, Collier D, Bernardo Md, Granero R, Karwautz A, Nacmias B, Penelo E, Ricca V, Sorbi S, Tchanturia K, Wagner G, Fernández-Aranda F.

Br J Nutr. 2009 Mar;101(6):909-18. doi: 10.1017/S0007114508047752. Epub 2008 Aug 28.

28.

Present and lifetime comorbidity of tobacco, alcohol and drug use in eating disorders: a European multicenter study.

Krug I, Treasure J, Anderluh M, Bellodi L, Cellini E, di Bernardo M, Granero R, Karwautz A, Nacmias B, Penelo E, Ricca V, Sorbi S, Tchanturia K, Wagner G, Collier D, Fernández-Aranda F.

Drug Alcohol Depend. 2008 Sep 1;97(1-2):169-79. doi: 10.1016/j.drugalcdep.2008.04.015. Epub 2008 Jun 20.

PMID:
18571341
29.

KIBRA gene variants are associated with episodic memory performance in subjective memory complaints.

Nacmias B, Bessi V, Bagnoli S, Tedde A, Cellini E, Piccini C, Sorbi S, Bracco L.

Neurosci Lett. 2008 May 9;436(2):145-7. doi: 10.1016/j.neulet.2008.03.008. Epub 2008 Mar 7.

PMID:
18378080
30.

Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease.

Poleggi A, Bizzarro A, Acciarri A, Antuono P, Bagnoli S, Cellini E, Forno GD, Giannattasio C, Lauria A, Matera MG, Nacmias B, Puopolo M, Seripa D, Sorbi S, Wekstein DR, Pocchiari M, Masullo C.

Eur J Neurol. 2008 Feb;15(2):173-8. doi: 10.1111/j.1468-1331.2007.02021.x.

PMID:
18217885
31.

Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders.

Mercader JM, Saus E, Agüera Z, Bayés M, Boni C, Carreras A, Cellini E, de Cid R, Dierssen M, Escaramís G, Fernández-Aranda F, Forcano L, Gallego X, González JR, Gorwood P, Hebebrand J, Hinney A, Nacmias B, Puig A, Ribasés M, Ricca V, Romo L, Sorbi S, Versini A, Gratacòs M, Estivill X.

Hum Mol Genet. 2008 May 1;17(9):1234-44. doi: 10.1093/hmg/ddn013. Epub 2008 Jan 18.

PMID:
18203754
32.

No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy.

Tedde A, Bagnoli S, Cellini E, Nacmias B, Piacentini S, Sorbi S.

Cell Mol Neurobiol. 2007 Nov;27(7):877-81. Epub 2007 Sep 11.

PMID:
17846883
33.

Mutational screening analysis of DHCR24/seladin-1 gene in Italian familial Alzheimer's disease.

Tedde A, Cellini E, Bagnoli S, Sorbi S, Peri A.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 5;147B(1):117-9.

PMID:
17579359
34.

Association of IL10 promoter polymorphism in Italian Alzheimer's disease.

Bagnoli S, Cellini E, Tedde A, Nacmias B, Piacentini S, Bessi V, Bracco L, Sorbi S.

Neurosci Lett. 2007 May 18;418(3):262-5. Epub 2007 Mar 19.

PMID:
17420099
35.

Morphometry and 1H-MR spectroscopy of the brain stem and cerebellum in three patients with fragile X-associated tremor/ataxia syndrome.

Ginestroni A, Guerrini L, Della Nave R, Tessa C, Cellini E, Dotti MT, Brunori P, De Stefano N, Piacentini S, Mascalchi M.

AJNR Am J Neuroradiol. 2007 Mar;28(3):486-8.

36.

Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations.

Brown AM, Gordon D, Lee H, Wavrant-De Vrièze F, Cellini E, Bagnoli S, Nacmias B, Sorbi S, Hardy J, Blass JP.

Neurochem Res. 2007 Apr-May;32(4-5):857-69. Epub 2007 Mar 7.

PMID:
17342416
37.

Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity.

Nacmias B, Bagnoli S, Tedde A, Cellini E, Bessi V, Guarnieri B, Ortensi L, Piacentini S, Bracco L, Sorbi S.

Arch Gerontol Geriatr. 2007 Sep-Oct;45(2):201-6. Epub 2006 Dec 19.

PMID:
17182125
38.

Association analysis of the paraoxonase-1 gene with Alzheimer's disease.

Cellini E, Tedde A, Bagnoli S, Nacmias B, Piacentini S, Bessi V, Bracco L, Sorbi S.

Neurosci Lett. 2006 Nov 20;408(3):199-202. Epub 2006 Sep 25.

PMID:
16996683
39.

Fragile X premutation with atypical symptoms at onset.

Cellini E, Forleo P, Ginestroni A, Nacmias B, Tedde A, Bagnoli S, Mascalchi M, Sorbi S, Piacentini S.

Arch Neurol. 2006 Aug;63(8):1135-8.

PMID:
16908740
40.

Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa.

Cellini E, Nacmias B, Brecelj-Anderluh M, Badía-Casanovas A, Bellodi L, Boni C, Di Bella D, Estivill X, Fernandez-Aranda F, Foulon C, Friedel S, Gabrovsek M, Gorwood P, Gratacos M, Guelfi J, Hebebrand J, Hinney A, Holliday J, Hu X, Karwautz A, Kipman A, Komel R, Rotella CM, Ribases M, Ricca V, Romo L, Tomori M, Treasure J, Wagner G, Collier DA, Sorbi S; EC Framework V 'Factors in Healthy Eating' consortium.

Psychiatr Genet. 2006 Apr;16(2):51-2. No abstract available.

PMID:
16538179
41.

Insulin degrading enzyme and alpha-3 catenin polymorphisms in Italian patients with Alzheimer disease.

Cellini E, Bagnoli S, Tedde A, Nacmias B, Piacentini S, Sorbi S.

Alzheimer Dis Assoc Disord. 2005 Oct-Dec;19(4):246-7. No abstract available.

PMID:
16327352
42.

Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits.

Bracco L, Piccini C, Moretti M, Mascalchi M, Sforza A, Nacmias B, Cellini E, Bagnoli S, Sorbi S.

Dement Geriatr Cogn Disord. 2005;20(6):358-66. Epub 2005 Sep 26.

PMID:
16192726
43.

Cystatin C and apoe polymorphisms in Italian Alzheimer's disease.

Nacmias B, Bagnoli S, Tedde A, Cellini E, Guarnieri BM, Bartoli A, Serio A, Piacentini S, Sorbi S.

Neurosci Lett. 2006 Jan 9;392(1-2):110-3. Epub 2005 Sep 26.

PMID:
16188386
44.

Lack of association between the CYP46 gene polymorphism and Italian late-onset sporadic Alzheimer's disease.

Tedde A, Rotondi M, Cellini E, Bagnoli S, Muratore L, Nacmias B, Sorbi S.

Neurobiol Aging. 2006 May;27(5):773.e1-773.e3. Epub 2005 Aug 1.

PMID:
16055229
45.

Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians.

Cellini E, Nacmias B, Olivieri F, Ortenzi L, Tedde A, Bagnoli S, Petruzzi C, Franceschi C, Sorbi S.

Mech Ageing Dev. 2005 Jun-Jul;126(6-7):826-8.

PMID:
15888337
46.

Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations.

Ribasés M, Gratacòs M, Fernández-Aranda F, Bellodi L, Boni C, Anderluh M, Cristina Cavallini M, Cellini E, Di Bella D, Erzegovesi S, Foulon C, Gabrovsek M, Gorwood P, Hebebrand J, Hinney A, Holliday J, Hu X, Karwautz A, Kipman A, Komel R, Nacmias B, Remschmidt H, Ricca V, Sorbi S, Tomori M, Wagner G, Treasure J, Collier DA, Estivill X.

Eur J Hum Genet. 2005 Apr;13(4):428-34.

47.

The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease.

Bagnoli S, Tedde A, Cellini E, Rotondi M, Nacmias B, Sorbi S.

Neurogenetics. 2005 Feb;6(1):53-4. Epub 2004 Dec 23. No abstract available. Erratum in: Neurogenetics. 2005 May;6(2):105.

PMID:
15616835
48.

Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease.

Nacmias B, Piccini C, Bagnoli S, Tedde A, Cellini E, Bracco L, Sorbi S.

Neurosci Lett. 2004 Sep 9;367(3):379-83.

PMID:
15337270
49.

Psychopathological traits and 5-HT2A receptor promoter polymorphism (-1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa.

Ricca V, Nacmias B, Boldrini M, Cellini E, di Bernardo M, Ravaldi C, Tedde A, Bagnoli S, Placidi GF, Rotella CM, Sorbi S.

Neurosci Lett. 2004 Jul 22;365(2):92-6.

PMID:
15245785
50.

Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia.

Cellini E, Forleo P, Nacmias B, Tedde A, Bagnoli S, Piacentini S, Sorbi S.

Ann Neurol. 2004 Jul;56(1):163; author reply 163-4. No abstract available.

PMID:
15236416

Supplemental Content

Loading ...
Support Center