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Items: 1 to 50 of 189

1.

Emotional ratings and skin conductance response to visual, auditory and haptic stimuli.

Gatti E, Calzolari E, Maggioni E, Obrist M.

Sci Data. 2018 Jun 26;5:180120. doi: 10.1038/sdata.2018.120.

2.

Unilateral spatial neglect after posterior parietal damage.

Vallar G, Calzolari E.

Handb Clin Neurol. 2018;151:287-312. doi: 10.1016/B978-0-444-63622-5.00014-0.

PMID:
29519463
3.

Multisensory and Modality-Specific Influences on Adaptation to Optical Prisms.

Calzolari E, Albini F, Bolognini N, Vallar G.

Front Hum Neurosci. 2017 Nov 22;11:568. doi: 10.3389/fnhum.2017.00568. eCollection 2017.

4.

Adaptation aftereffects reveal that tactile distance is a basic somatosensory feature.

Calzolari E, Azañón E, Danvers M, Vallar G, Longo MR.

Proc Natl Acad Sci U S A. 2017 Apr 25;114(17):4555-4560. doi: 10.1073/pnas.1614979114. Epub 2017 Apr 10.

5.

[Validation of an algorithm for identifying cases with congenital malformations by using hospital discharge records].

Astolfi G, Ricci P, Calzolari E, Neville A, Pironi V, Santoro M, Bianchi F.

Epidemiol Prev. 2016 Mar-Apr;40(2):124-30. doi: 10.19191/EP16.2.P124.067. Italian.

6.

Does maternal exposure to benzene and PM10 during pregnancy increase the risk of congenital anomalies? A population-based case-control study.

Vinceti M, Malagoli C, Malavolti M, Cherubini A, Maffeis G, Rodolfi R, Heck JE, Astolfi G, Calzolari E, Nicolini F.

Sci Total Environ. 2016 Jan 15;541:444-450. doi: 10.1016/j.scitotenv.2015.09.051. Epub 2015 Sep 26.

7.

Effect of prism adaptation on thermoregulatory control in humans.

Calzolari E, Gallace A, Moseley GL, Vallar G.

Behav Brain Res. 2016 Jan 1;296:339-350. doi: 10.1016/j.bbr.2015.08.036. Epub 2015 Oct 9.

PMID:
26354443
8.

Restoring abnormal aftereffects of prismatic adaptation through neuromodulation.

Calzolari E, Bolognini N, Casati C, Marzoli SB, Vallar G.

Neuropsychologia. 2015 Jul;74:162-9. doi: 10.1016/j.neuropsychologia.2015.04.022. Epub 2015 Apr 23.

PMID:
25912762
9.

Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study.

McGivern MR, Best KE, Rankin J, Wellesley D, Greenlees R, Addor MC, Arriola L, de Walle H, Barisic I, Beres J, Bianchi F, Calzolari E, Doray B, Draper ES, Garne E, Gatt M, Haeusler M, Khoshnood B, Klungsoyr K, Latos-Bielenska A, O'Mahony M, Braz P, McDonnell B, Mullaney C, Nelen V, Queisser-Luft A, Randrianaivo H, Rissmann A, Rounding C, Sipek A, Thompson R, Tucker D, Wertelecki W, Martos C.

Arch Dis Child Fetal Neonatal Ed. 2015 Mar;100(2):F137-44. doi: 10.1136/archdischild-2014-306174. Epub 2014 Nov 19.

PMID:
25411443
10.

Holt Oram syndrome: a registry-based study in Europe.

Barisic I, Boban L, Greenlees R, Garne E, Wellesley D, Calzolari E, Addor MC, Arriola L, Bergman JE, Braz P, Budd JL, Gatt M, Haeusler M, Khoshnood B, Klungsoyr K, McDonnell B, Nelen V, Pierini A, Queisser-Wahrendorf A, Rankin J, Rissmann A, Rounding C, Tucker D, Verellen-Dumoulin C, Dolk H.

Orphanet J Rare Dis. 2014 Oct 25;9:156. doi: 10.1186/s13023-014-0156-y.

11.

Meckel-Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe.

Barisic I, Boban L, Loane M, Garne E, Wellesley D, Calzolari E, Dolk H, Addor MC, Bergman JE, Braz P, Draper ES, Haeusler M, Khoshnood B, Klungsoyr K, Pierini A, Queisser-Luft A, Rankin J, Rissmann A, Verellen-Dumoulin C.

Eur J Hum Genet. 2015 Jun;23(6):746-52. doi: 10.1038/ejhg.2014.174. Epub 2014 Sep 3.

12.

Hirschsprung's disease prevalence in Europe: a register based study.

Best KE, Addor MC, Arriola L, Balku E, Barisic I, Bianchi F, Calzolari E, Curran R, Doray B, Draper E, Garne E, Gatt M, Haeusler M, Bergman J, Khoshnood B, Klungsoyr K, Martos C, Materna-Kiryluk A, Matias Dias C, McDonnell B, Mullaney C, Nelen V, O'Mahony M, Queisser-Luft A, Randrianaivo H, Rissmann A, Rounding C, Sipek A, Thompson R, Tucker D, Wellesley D, Zymak-Zakutnia N, Rankin J.

Birth Defects Res A Clin Mol Teratol. 2014 Sep;100(9):695-702. doi: 10.1002/bdra.23269. Epub 2014 Jul 26.

PMID:
25066220
13.

Prenatal diagnosis and epidemiology of multicystic kidney dysplasia in Europe.

Winding L, Loane M, Wellesley D, Addor MC, Arriola L, Bakker MK, Bianchi F, Calzolari E, Gatt M, Haeusler M, Lelong N, Mullaney C, Scarano G, Tucker D, Wiesel A, Garne E.

Prenat Diagn. 2014 Nov;34(11):1093-8. doi: 10.1002/pd.4433. Epub 2014 Jul 2.

PMID:
24916896
14.

Risk of birth defects associated with maternal pregestational diabetes.

Vinceti M, Malagoli C, Rothman KJ, Rodolfi R, Astolfi G, Calzolari E, Puccini A, Bertolotti M, Lunt M, Paterlini L, Martini M, Nicolini F.

Eur J Epidemiol. 2014 Jun;29(6):411-8. doi: 10.1007/s10654-014-9913-4. Epub 2014 May 27.

PMID:
24861339
15.

Epidemiology of multiple congenital anomalies in Europe: a EUROCAT population-based registry study.

Calzolari E, Barisic I, Loane M, Morris J, Wellesley D, Dolk H, Addor MC, Arriola L, Bianchi F, Neville AJ, Budd JL, Klungsoyr K, Khoshnood B, McDonnell B, Nelen V, Queisser-Luft A, Rankin J, Rissmann A, Rounding C, Tucker D, Verellen-Dumoulin C, de Walle H, Garne E.

Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):270-6. doi: 10.1002/bdra.23240. Epub 2014 Apr 11.

PMID:
24723551
16.

European recommendations for primary prevention of congenital anomalies: a joined effort of EUROCAT and EUROPLAN projects to facilitate inclusion of this topic in the National Rare Disease Plans.

Taruscio D, Arriola L, Baldi F, Barisic I, Bermejo-Sánchez E, Bianchi F, Calzolari E, Carbone P, Curran R, Garne E, Gatt M, Latos-Bieleńska A, Khoshnood B, Irgens L, Mantovani A, Martínez-Frías ML, Neville A, Rißmann A, Ruggeri S, Wellesley D, Dolk H.

Public Health Genomics. 2014;17(2):115-23. doi: 10.1159/000360602. Epub 2014 Apr 3.

PMID:
24714026
17.

Seasonality of congenital anomalies in Europe.

Luteijn JM, Dolk H, Addor MC, Arriola L, Barisic I, Bianchi F, Calzolari E, Draper E, Garne E, Gatt M, Haeusler M, Khoshnood B, McDonnell B, Nelen V, O'Mahony M, Mullaney C, Queisser-Luft A, Rankin J, Tucker D, Verellen-Dumoulin C, de Walle H, Yevtushok L.

Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):260-9. doi: 10.1002/bdra.23231. Epub 2014 Mar 17.

PMID:
24639385
18.

Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe.

Barisic I, Odak L, Loane M, Garne E, Wellesley D, Calzolari E, Dolk H, Addor MC, Arriola L, Bergman J, Bianca S, Doray B, Khoshnood B, Klungsoyr K, McDonnell B, Pierini A, Rankin J, Rissmann A, Rounding C, Queisser-Luft A, Scarano G, Tucker D.

Eur J Hum Genet. 2014 Aug;22(8):1026-33. doi: 10.1038/ejhg.2013.287. Epub 2014 Jan 8.

19.

[Using hospital discharge records, birth certificates and a birth defects registry for epidemiological and public health purposes: experience in Emilia-Romagna region (northern Italy)].

Astolfi G, Bianchi F, Lupi C, Napoli N, Neville A, Verdini E, Verzola A, Calzolari E.

Epidemiol Prev. 2013 Jul-Oct;37(4-5):279-88. Italian.

PMID:
24293493
20.

Prenatal genetic counseling referrals for advanced maternal age: still room for improvement.

Pompilii E, Astolfi G, Calabrese O, Calzolari E, Ferlini A, Lucci M, Parmeggiani G, Seri M, Baroncini A.

Prenat Diagn. 2014 Jan;34(1):71-4.

PMID:
24166136
21.

Anorectal malformations and pregnancy-related disorders: a registry-based case-control study in 17 European regions.

Wijers CH, van Rooij IA, Bakker MK, Marcelis CL, Addor MC, Barisic I, Béres J, Bianca S, Bianchi F, Calzolari E, Greenlees R, Lelong N, Latos-Bielenska A, Dias CM, McDonnell R, Mullaney C, Nelen V, O'Mahony M, Queisser-Luft A, Rankin J, Zymak-Zakutnia N, de Blaauw I, Roeleveld N, de Walle HE.

BJOG. 2013 Aug;120(9):1066-74. doi: 10.1111/1471-0528.12235. Epub 2013 Apr 10.

22.

Fraser syndrome: epidemiological study in a European population.

Barisic I, Odak L, Loane M, Garne E, Wellesley D, Calzolari E, Dolk H, Addor MC, Arriola L, Bergman J, Bianca S, Boyd PA, Draper ES, Gatt M, Haeusler M, Khoshnood B, Latos-Bielenska A, McDonnell B, Pierini A, Rankin J, Rissmann A, Queisser-Luft A, Verellen-Dumoulin C, Stone D, Tenconi R.

Am J Med Genet A. 2013 May;161A(5):1012-8. doi: 10.1002/ajmg.a.35839. Epub 2013 Mar 26.

PMID:
23532946
23.

An epidemiological survey of Mycoplasma hominis and Ureaplasma urealyticum in gynaecological outpatients, Rome, Italy.

Verteramo R, Patella A, Calzolari E, Recine N, Marcone V, Osborn J, Chiarini F, Degener AM.

Epidemiol Infect. 2013 Dec;141(12):2650-7. doi: 10.1017/S0950268813000277. Epub 2013 Feb 28.

PMID:
23445723
24.

Exploring the effects of ecological activities during exposure to optical prisms in healthy individuals.

Fortis P, Ronchi R, Calzolari E, Gallucci M, Vallar G.

Front Hum Neurosci. 2013 Feb 12;7:29. doi: 10.3389/fnhum.2013.00029. eCollection 2013.

25.

Epidemiology of small intestinal atresia in Europe: a register-based study.

Best KE, Tennant PW, Addor MC, Bianchi F, Boyd P, Calzolari E, Dias CM, Doray B, Draper E, Garne E, Gatt M, Greenlees R, Haeusler M, Khoshnood B, McDonnell B, Mullaney C, Nelen V, Randrianaivo H, Rissmann A, Salvador J, Tucker D, Wellesly D, Rankin J.

Arch Dis Child Fetal Neonatal Ed. 2012 Sep;97(5):F353-8. doi: 10.1136/fetalneonatal-2011-300631.

PMID:
22933095
26.

Recent decrease in the prevalence of congenital heart defects in Europe.

Khoshnood B, Loane M, Garne E, Addor MC, Arriola L, Bakker M, Barisic I, Bianca S, Boyd P, Calzolari E, Doray B, Draper E, Gatt M, Haeusler M, Melve KK, Latos-Bielenska A, McDonnell B, Mullaney C, Nelen V, O'Mahony M, Pierini A, Queisser-Luft A, Randrianaivo H, Rankin J, Rissmann A, Salvador J, Tucker D, Verellen-Dumoulin C, Wellesley D, Zymak-Zakutnya N, Dolk H.

J Pediatr. 2013 Jan;162(1):108-13.e2. doi: 10.1016/j.jpeds.2012.06.035. Epub 2012 Jul 24.

PMID:
22835879
27.

Maternal exposure to magnetic fields from high-voltage power lines and the risk of birth defects.

Malagoli C, Crespi CM, Rodolfi R, Signorelli C, Poli M, Zanichelli P, Fabbi S, Teggi S, Garavelli L, Astolfi G, Calzolari E, Lucenti C, Vinceti M.

Bioelectromagnetics. 2012 Jul;33(5):405-9.

PMID:
22826845
28.

Epidemiology of Chlamydia trachomatis endocervical infection in a previously unscreened population in Rome, Italy, 2000 to 2009.

Marcone V, Recine N, Gallinelli C, Nicosia R, Lichtner M, Degener AM, Chiarini F, Calzolari E, Vullo V.

Euro Surveill. 2012 Jun 21;17(25). pii: 20203.

29.

Trihalomethanes, chlorite, chlorate in drinking water and risk of congenital anomalies: a population-based case-control study in Northern Italy.

Righi E, Bechtold P, Tortorici D, Lauriola P, Calzolari E, Astolfi G, Nieuwenhuijsen MJ, Fantuzzi G, Aggazzotti G.

Environ Res. 2012 Jul;116:66-73. doi: 10.1016/j.envres.2012.04.014. Epub 2012 May 9.

PMID:
22578809
30.

Spectrum of congenital anomalies in pregnancies with pregestational diabetes.

Garne E, Loane M, Dolk H, Barisic I, Addor MC, Arriola L, Bakker M, Calzolari E, Matias Dias C, Doray B, Gatt M, Melve KK, Nelen V, O'Mahony M, Pierini A, Randrianaivo-Ranjatoelina H, Rankin J, Rissmann A, Tucker D, Verellun-Dumoulin C, Wiesel A.

Birth Defects Res A Clin Mol Teratol. 2012 Mar;94(3):134-40. doi: 10.1002/bdra.22886. Epub 2012 Feb 28.

PMID:
22371321
31.

Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions.

Pedersen RN, Calzolari E, Husby S, Garne E; EUROCAT Working group.

Arch Dis Child. 2012 Mar;97(3):227-32. doi: 10.1136/archdischild-2011-300597. Epub 2012 Jan 13.

PMID:
22247246
32.

Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe.

Wellesley D, Dolk H, Boyd PA, Greenlees R, Haeusler M, Nelen V, Garne E, Khoshnood B, Doray B, Rissmann A, Mullaney C, Calzolari E, Bakker M, Salvador J, Addor MC, Draper E, Rankin J, Tucker D.

Eur J Hum Genet. 2012 May;20(5):521-6. doi: 10.1038/ejhg.2011.246. Epub 2012 Jan 11.

33.

[Congenital malformations in Italy. A network to monitor the phenomenon].

Carbone P, Taruscio D, Bianchi F, Calzolari E, Scarano G; Coordinamento Nazionale dei Registri delle Malformazioni Congenite.

Epidemiol Prev. 2011 Sep-Dec;35(5-6 Suppl 2):90-1. Italian. No abstract available.

34.

Paper 5: Surveillance of multiple congenital anomalies: implementation of a computer algorithm in European registers for classification of cases.

Garne E, Dolk H, Loane M, Wellesley D, Barisic I, Calzolari E, Densem J; EUROCAT Working Group.

Birth Defects Res A Clin Mol Teratol. 2011 Mar;91 Suppl 1:S44-50. doi: 10.1002/bdra.20777. Epub 2011 Mar 7. Review.

PMID:
21384529
35.

Paper 6: EUROCAT member registries: organization and activities.

Greenlees R, Neville A, Addor MC, Amar E, Arriola L, Bakker M, Barisic I, Boyd PA, Calzolari E, Doray B, Draper E, Vollset SE, Garne E, Gatt M, Haeusler M, Kallen K, Khoshnood B, Latos-Bielenska A, Martinez-Frias ML, Materna-Kiryluk A, Dias CM, McDonnell B, Mullaney C, Nelen V, O'Mahony M, Pierini A, Queisser-Luft A, Randrianaivo-Ranjatoélina H, Rankin J, Rissmann A, Ritvanen A, Salvador J, Sipek A, Tucker D, Verellen-Dumoulin C, Wellesley D, Wertelecki W.

Birth Defects Res A Clin Mol Teratol. 2011 Mar;91 Suppl 1:S51-S100. doi: 10.1002/bdra.20775. Epub 2011 Mar 4. Review.

PMID:
21381185
36.

Long-term vaginal administration of Lactobacillus rhamnosus as a complementary approach to management of bacterial vaginosis.

Marcone V, Rocca G, Lichtner M, Calzolari E.

Int J Gynaecol Obstet. 2010 Sep;110(3):223-6. doi: 10.1016/j.ijgo.2010.04.025. Epub 2010 Jun 22.

PMID:
20573348
37.

Human Papillomaviruses and genital co-infections in gynaecological outpatients.

Verteramo R, Pierangeli A, Mancini E, Calzolari E, Bucci M, Osborn J, Nicosia R, Chiarini F, Antonelli G, Degener AM.

BMC Infect Dis. 2009 Feb 12;9:16. doi: 10.1186/1471-2334-9-16.

39.

The Italian external quality assessment scheme in classical cytogenetics: four years of activity.

Floridia G, Falbo V, Censi F, Tosto F, Salvatore M, Baroncini A, Battaglia P, Conti A, Donti E, La Starza R, Nitsch L, Pierluigi M, Piombo G, Susca F, Mancini M, Mecucci C, Calzolari E, Dagna Bricarelli F, Guanti G, Taruscio D.

Community Genet. 2008;11(5):295-303. doi: 10.1159/000121401. Epub 2008 May 20.

PMID:
18493128
40.

Trichomonas vaginalis infection: risk indicators among women attending for routine gynecologic examination.

Verteramo R, Calzolari E, Degener AM, Masciangelo R, Patella A.

J Obstet Gynaecol Res. 2008 Apr;34(2):233-7. doi: 10.1111/j.1447-0756.2007.00692.x.

PMID:
18412787
41.

Exclusion of COL2A1 and VDR as developmental dysplasia of the hip genes.

Rubini M, Cavallaro A, Calzolari E, Bighetti G, Sollazzo V.

Clin Orthop Relat Res. 2008 Apr;466(4):878-83. doi: 10.1007/s11999-008-0120-z. Epub 2008 Feb 21.

42.

Paracentric inversion of Yq and review of the literature.

Aiello V, Astolfi N, Gruppioni R, Buldrini B, Prontera P, Bonfatti A, Sensi A, Calzolari E.

Genet Couns. 2007;18(4):379-82. Review.

PMID:
18286818
43.

Descriptive epidemiology of Cornelia de Lange syndrome in Europe.

Barisic I, Tokic V, Loane M, Bianchi F, Calzolari E, Garne E, Wellesley D, Dolk H; EUROCAT Working Group.

Am J Med Genet A. 2008 Jan 1;146A(1):51-9.

PMID:
18074387
44.

Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype.

Sensi A, Prontera P, Buldrini B, Palma S, Aiello V, Gruppioni R, Calzolari E, Volinia S, Martini A.

Am J Med Genet A. 2008 Jan 1;146A(1):110-5.

PMID:
18074369
45.

Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion.

Prontera P, Aiello V, Toschi M, Turci A, Gruppioni R, Buldrini B, Zago S, Bonfatti A, Donti E, Calzolari E, Sensi A.

Genet Couns. 2007;18(3):309-15.

PMID:
18019372
46.

In vitro short-term test evaluation of catecholestrogens genotoxicity.

Rossi D, Aiello V, Mazzoni L, Sensi A, Calzolari E.

J Steroid Biochem Mol Biol. 2007 Jun-Jul;105(1-5):98-105. Epub 2007 May 17.

PMID:
17590328
47.

FGFR3 mutation in thanatophoric dysplasia type 1 with bilateral cystic renal dysplasia: coincidence or a new association?

Prontera P, Sensi A, Pilu G, Baldi M, Baffico M, Bonasoni R, Calzolari E.

Genet Couns. 2006;17(4):407-12.

PMID:
17375526
48.

Associated anomalies in multi-malformed infants with cleft lip and palate: An epidemiologic study of nearly 6 million births in 23 EUROCAT registries.

Calzolari E, Pierini A, Astolfi G, Bianchi F, Neville AJ, Rivieri F.

Am J Med Genet A. 2007 Mar 15;143A(6):528-37.

PMID:
17286264
49.

Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories.

Ferlini A, Ravani A, Venturoli A, Trabanelli C, Masieri MT, Brandi A, Dolcini B, Rimessi P, Gualandi F, Calzolari E.

Prenat Diagn. 2006 Oct;26(10):989-91. No abstract available.

PMID:
17029302
50.

Familial occurrence of multiple pterygium syndrome: expression in a heterozygote of the recessive form or variability of the dominant form?

Prontera P, Sensi A, Merlo L, Garani G, Cocchi G, Calzolari E.

Am J Med Genet A. 2006 Oct 15;140(20):2227-30.

PMID:
16964621

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