Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 56

1.

Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.

Cameron-Christie SR, Wells CF, Simon M, Wessels M, Tang CZN, Wei W, Takei R, Aarts-Tesselaar C, Sandaradura S, Sillence DO, Cordier MP, Veenstra-Knol HE, Cassina M, Ludwig K, Trevisson E, Bahlo M, Markie DM, Jenkins ZA, Robertson SP.

Am J Hum Genet. 2019 Sep 5;105(3):669. doi: 10.1016/j.ajhg.2019.08.007. No abstract available.

2.

Dysfunctional coping is related to impaired skin-related QoL and psychological distress in Neurofibromatosis type 1 patients with major skin involvement.

Bottesi G, Spoto A, Trevisson E, Zuccarello D, Vidotto G, Cassina M, Clementi M.

Br J Dermatol. 2019 Jul 22. doi: 10.1111/bjd.18363. [Epub ahead of print]

PMID:
31329288
3.

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

Watson HJ, Yilmaz Z, Thornton LM, Hübel C, Coleman JRI, Gaspar HA, Bryois J, Hinney A, Leppä VM, Mattheisen M, Medland SE, Ripke S, Yao S, Giusti-Rodríguez P; Anorexia Nervosa Genetics Initiative, Hanscombe KB, Purves KL; Eating Disorders Working Group of the Psychiatric Genomics Consortium, Adan RAH, Alfredsson L, Ando T, Andreassen OA, Baker JH, Berrettini WH, Boehm I, Boni C, Perica VB, Buehren K, Burghardt R, Cassina M, Cichon S, Clementi M, Cone RD, Courtet P, Crow S, Crowley JJ, Danner UN, Davis OSP, de Zwaan M, Dedoussis G, Degortes D, DeSocio JE, Dick DM, Dikeos D, Dina C, Dmitrzak-Weglarz M, Docampo E, Duncan LE, Egberts K, Ehrlich S, Escaramís G, Esko T, Estivill X, Farmer A, Favaro A, Fernández-Aranda F, Fichter MM, Fischer K, Föcker M, Foretova L, Forstner AJ, Forzan M, Franklin CS, Gallinger S, Giegling I, Giuranna J, Gonidakis F, Gorwood P, Mayora MG, Guillaume S, Guo Y, Hakonarson H, Hatzikotoulas K, Hauser J, Hebebrand J, Helder SG, Herms S, Herpertz-Dahlmann B, Herzog W, Huckins LM, Hudson JI, Imgart H, Inoko H, Janout V, Jiménez-Murcia S, Julià A, Kalsi G, Kaminská D, Kaprio J, Karhunen L, Karwautz A, Kas MJH, Kennedy JL, Keski-Rahkonen A, Kiezebrink K, Kim YR, Klareskog L, Klump KL, Knudsen GPS, La Via MC, Le Hellard S, Levitan RD, Li D, Lilenfeld L, Lin BD, Lissowska J, Luykx J, Magistretti PJ, Maj M, Mannik K, Marsal S, Marshall CR, Mattingsdal M, McDevitt S, McGuffin P, Metspalu A, Meulenbelt I, Micali N, Mitchell K, Monteleone AM, Monteleone P, Munn-Chernoff MA, Nacmias B, Navratilova M, Ntalla I, O'Toole JK, Ophoff RA, Padyukov L, Palotie A, Pantel J, Papezova H, Pinto D, Rabionet R, Raevuori A, Ramoz N, Reichborn-Kjennerud T, Ricca V, Ripatti S, Ritschel F, Roberts M, Rotondo A, Rujescu D, Rybakowski F, Santonastaso P, Scherag A, Scherer SW, Schmidt U, Schork NJ, Schosser A, Seitz J, Slachtova L, Slagboom PE, Slof-Op 't Landt MCT, Slopien A, Sorbi S, Świątkowska B, Szatkiewicz JP, Tachmazidou I, Tenconi E, Tortorella A, Tozzi F, Treasure J, Tsitsika A, Tyszkiewicz-Nwafor M, Tziouvas K, van Elburg AA, van Furth EF, Wagner G, Walton E, Widen E, Zeggini E, Zerwas S, Zipfel S, Bergen AW, Boden JM, Brandt H, Crawford S, Halmi KA, Horwood LJ, Johnson C, Kaplan AS, Kaye WH, Mitchell JE, Olsen CM, Pearson JF, Pedersen NL, Strober M, Werge T, Whiteman DC, Woodside DB, Stuber GD, Gordon S, Grove J, Henders AK, Juréus A, Kirk KM, Larsen JT, Parker R, Petersen L, Jordan J, Kennedy M, Montgomery GW, Wade TD, Birgegård A, Lichtenstein P, Norring C, Landén M, Martin NG, Mortensen PB, Sullivan PF, Breen G, Bulik CM.

Nat Genet. 2019 Aug;51(8):1207-1214. doi: 10.1038/s41588-019-0439-2. Epub 2019 Jul 15.

PMID:
31308545
4.

Prevalence and survival of patients with anorectal malformations: A population-based study.

Cassina M, Fascetti Leon F, Ruol M, Chiarenza SF, Scirè G, Midrio P, Clementi M, Gamba P.

J Pediatr Surg. 2019 Mar 16. pii: S0022-3468(19)30205-2. doi: 10.1016/j.jpedsurg.2019.03.004. [Epub ahead of print]

PMID:
30935729
5.

The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromas.

Trevisson E, Morbidoni V, Forzan M, Daolio C, Fumini V, Parrozzani R, Cassina M, Midena E, Salviati L, Clementi M.

Mol Genet Genomic Med. 2019 May;7(5):e616. doi: 10.1002/mgg3.616. Epub 2019 Mar 6.

6.

Mutational spectrum and clinical signatures in 114 families with hereditary multiple osteochondromas: insights into molecular properties of selected exostosin variants.

Fusco C, Nardella G, Fischetto R, Copetti M, Petracca A, Annunziata F, Augello B, D'Asdia MC, Petrucci S, Mattina T, Rella A, Cassina M, Bengala M, Biagini T, Causio FA, Caldarini C, Brancati F, De Luca A, Guarnieri V, Micale L, D'Agruma L, Castori M.

Hum Mol Genet. 2019 Jul 1;28(13):2133-2142. doi: 10.1093/hmg/ddz046.

PMID:
30806661
7.

Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.

Cameron-Christie SR, Wells CF, Simon M, Wessels M, Tang CZN, Wei W, Takei R, Aarts-Tesselaar C, Sandaradura S, Sillence DO, Cordier MP, Veenstra-Knol HE, Cassina M, Ludwig K, Trevisson E, Bahlo M, Markie DM, Jenkins ZA, Robertson SP.

Am J Hum Genet. 2018 Jun 7;102(6):1115-1125. doi: 10.1016/j.ajhg.2018.04.008. Epub 2018 May 24. Erratum in: Am J Hum Genet. 2019 Sep 5;105(3):669.

8.

Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive cases.

Cassina M, Calò A, Salviati L, Alghisi A, Montaldi A, Clementi M.

Eur J Obstet Gynecol Reprod Biol. 2018 Feb;221:23-27. doi: 10.1016/j.ejogrb.2017.12.012. Epub 2017 Dec 7.

PMID:
29232625
9.

Pregnancy outcomes in women on metformin for diabetes or other indications among those seeking teratology information services.

Panchaud A, Rousson V, Vial T, Bernard N, Baud D, Amar E, De Santis M, Pistelli A, Dautriche A, Beau-Salinas F, Cassina M, Dunstan H, Passier A, Kaplan YC, Duman MK, Maňáková E, Eleftheriou G, Klinger G, Winterfeld U, Rothuizen LE, Buclin T, Csajka C, Hernandez-Diaz S.

Br J Clin Pharmacol. 2018 Mar;84(3):568-578. doi: 10.1111/bcp.13481. Epub 2018 Jan 14.

10.

Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function.

Vazquez Fonseca L, Doimo M, Calderan C, Desbats MA, Acosta MJ, Cerqua C, Cassina M, Ashraf S, Hildebrandt F, Sartori G, Navas P, Trevisson E, Salviati L.

Hum Mutat. 2018 Mar;39(3):406-414. doi: 10.1002/humu.23376. Epub 2017 Dec 18.

11.

Catechol-O-Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta-Analysis of Previously Published Studies.

Collantoni E, Solmi M, Gallicchio D, Santonastaso P, Meneguzzo P, Carvalho AF, Stubbs B, Clementi M, Pinato C, Forzan M, Cassina M, Fontana F, Piva I, Siani R, Salvo P, Tenconi E, Veronese N, Correll CU, Favaro A.

Eur Eat Disord Rev. 2017 Nov;25(6):524-532. doi: 10.1002/erv.2555.

PMID:
29057600
12.

Effect of potassium and manganese phosphites in the control of Pythium damping-off in soybean: a feasible alternative to fungicide seed treatments.

Carmona MA, Sautua FJ, Grijalba PE, Cassina M, Pérez-Hernández O.

Pest Manag Sci. 2018 Feb;74(2):366-374. doi: 10.1002/ps.4714. Epub 2017 Oct 9.

PMID:
28842951
13.

Natural history of optic pathway gliomas in a cohort of unselected patients affected by Neurofibromatosis 1.

Trevisson E, Cassina M, Opocher E, Vicenzi V, Lucchetta M, Parrozzani R, Miglionico G, Mardari R, Viscardi E, Midena E, Clementi M.

J Neurooncol. 2017 Sep;134(2):279-287. doi: 10.1007/s11060-017-2517-6. Epub 2017 Jun 2.

PMID:
28577031
14.

RETINAL VASCULAR ABNORMALITIES IN A LARGE COHORT OF PATIENTS AFFECTED BY NEUROFIBROMATOSIS TYPE 1: A Study Using Optical Coherence Tomography Angiography.

Parrozzani R, Pilotto E, Clementi M, Frizziero L, Leonardi F, Convento E, Miglionico G, Pulze S, Perrini P, Trevisson E, Cassina M, Midena E.

Retina. 2018 Mar;38(3):585-593. doi: 10.1097/IAE.0000000000001578.

PMID:
28248826
15.

A synonymous splicing mutation in the SF3B4 gene segregates in a family with highly variable Nager syndrome.

Cassina M, Cerqua C, Rossi S, Salviati L, Martini A, Clementi M, Trevisson E.

Eur J Hum Genet. 2017 Feb;25(3):371-375. doi: 10.1038/ejhg.2016.176. Epub 2016 Dec 14.

16.

Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations.

Cao M, Donà M, Lucia Valentino M, Semplicini C, Maresca A, Cassina M, Torraco A, Galletta E, Manfioli V, Sorarù G, Carelli V, Stramare R, Bertini E, Carrozzo R, Salviati L, Pegoraro E.

Neurogenetics. 2017 Jan;18(1):69. doi: 10.1007/s10048-016-0501-5. No abstract available.

PMID:
27913898
17.

Human teratogens and genetic phenocopies. Understanding pathogenesis through human genes mutation.

Cassina M, Cagnoli GA, Zuccarello D, Di Gianantonio E, Clementi M.

Eur J Med Genet. 2017 Jan;60(1):22-31. doi: 10.1016/j.ejmg.2016.09.011. Epub 2016 Sep 14.

PMID:
27639441
18.

The COQ2 genotype predicts the severity of coenzyme Q10 deficiency.

Desbats MA, Morbidoni V, Silic-Benussi M, Doimo M, Ciminale V, Cassina M, Sacconi S, Hirano M, Basso G, Pierrel F, Navas P, Salviati L, Trevisson E.

Hum Mol Genet. 2016 Oct 1;25(19):4256-4265. doi: 10.1093/hmg/ddw257. Epub 2016 Aug 4.

PMID:
27493029
19.

Response to: Papetti et al., "The crucial role of FBXO28 in the pathogenesis of the 1q41q42 microdeletion syndrome".

Cassina M.

Am J Med Genet A. 2016 Nov;170(11):3054. doi: 10.1002/ajmg.a.37742. Epub 2016 May 13. No abstract available.

PMID:
27177014
20.

Erratum to: A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.

Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MT, Melis D, Manfredini E, Ferrero GB, Pecile V, Larizza L.

Clin Epigenetics. 2016 Apr 21;8:40. doi: 10.1186/s13148-016-0206-5. eCollection 2016. No abstract available.

21.

A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.

Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MT, Melis D, Manfredini E, Ferrero GB, Pecile V, Larizza L.

Clin Epigenetics. 2016 Mar 1;8:23. doi: 10.1186/s13148-016-0183-8. eCollection 2016. Erratum in: Clin Epigenetics. 2016;8:40.

22.

Prevalence, characteristics, and survival of children with esophageal atresia: A 32-year population-based study including 1,417,724 consecutive newborns.

Cassina M, Ruol M, Pertile R, Midrio P, Piffer S, Vicenzi V, Saugo M, Stocco CF, Gamba P, Clementi M.

Birth Defects Res A Clin Mol Teratol. 2016 Jul;106(7):542-8. doi: 10.1002/bdra.23493. Epub 2016 Mar 2.

PMID:
26931365
23.

Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations.

Cao M, Donà M, Valentino ML, Semplicini C, Maresca A, Cassina M, Torraco A, Galletta E, Manfioli V, Sorarù G, Carelli V, Stramare R, Bertini E, Carozzo R, Salviati L, Pegoraro E.

Neurogenetics. 2016 Apr;17(2):143. doi: 10.1007/s10048-016-0475-3. No abstract available.

PMID:
26924555
24.

Serotonin transporter gene polymorphism in eating disorders: Data from a new biobank and META-analysis of previous studies.

Solmi M, Gallicchio D, Collantoni E, Correll CU, Clementi M, Pinato C, Forzan M, Cassina M, Fontana F, Giannunzio V, Piva I, Siani R, Salvo P, Santonastaso P, Tenconi E, Veronese N, Favaro A.

World J Biol Psychiatry. 2016 Jun;17(4):244-57. doi: 10.3109/15622975.2015.1126675. Epub 2016 Feb 19. Review.

PMID:
26895183
25.

Clinical and genetic correlates of decision making in anorexia nervosa.

Tenconi E, Degortes D, Clementi M, Collantoni E, Pinato C, Forzan M, Cassina M, Santonastaso P, Favaro A.

J Clin Exp Neuropsychol. 2016;38(3):327-37. doi: 10.1080/13803395.2015.1112878. Epub 2015 Dec 29.

PMID:
26713494
26.

Functional connectivity correlates of response inhibition impairment in anorexia nervosa.

Collantoni E, Michelon S, Tenconi E, Degortes D, Titton F, Manara R, Clementi M, Pinato C, Forzan M, Cassina M, Santonastaso P, Favaro A.

Psychiatry Res Neuroimaging. 2016 Jan 30;247:9-16. doi: 10.1016/j.pscychresns.2015.11.008. Epub 2015 Dec 2.

PMID:
26655584
27.

Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations.

Cao M, Donà M, Valentino ML, Valentino L, Semplicini C, Maresca A, Cassina M, Torraco A, Galletta E, Manfioli V, Sorarù G, Carelli V, Stramare R, Bertini E, Carrozzo R, Salviati L, Pegoraro E.

Neurogenetics. 2016 Jan;17(1):65-70. doi: 10.1007/s10048-015-0465-x. Epub 2015 Nov 10. Erratum in: Neurogenetics. 2016 Apr;17(2):143. Valentino, Lucia [Corrected to Valentino, M. Lucia]. Neurogenetics. 2017 Jan;18(1):69. Carozzo, Rosalba [Corrected to Carrozzo, Rosalba].

PMID:
26556812
28.

FBXO28 is a critical gene of the 1q41q42 microdeletion syndrome.

Cassina M, Rigon C, Casarin A, Vicenzi V, Salviati L, Clementi M.

Am J Med Genet A. 2015 Jun;167(6):1418-20. doi: 10.1002/ajmg.a.37033. Epub 2015 Apr 21. No abstract available.

PMID:
25900767
29.

Validation of CFTR intronic variants identified during cystic fibrosis population screening by a minigene splicing assay.

Giorgi G, Casarin A, Trevisson E, Donà M, Cassina M, Graziano C, Picci L, Clementi M, Salviati L.

Clin Chem Lab Med. 2015 Oct;53(11):1719-23. doi: 10.1515/cclm-2014-1047.

PMID:
25781545
30.

Multigram synthesis and in vivo efficacy studies of a novel multitarget anti-Alzheimer's compound.

Sola I, Viayna E, Gómez T, Galdeano C, Cassina M, Camps P, Romeo M, Diomede L, Salmona M, Franco P, Schaeffer M, Colantuono D, Robin D, Brunner D, Taub N, Hutter-Paier B, Muñoz-Torrero D.

Molecules. 2015 Mar 10;20(3):4492-515. doi: 10.3390/molecules20034492.

31.

Forkhead box G1 gene haploinsufficiency: an emerging cause of dyskinetic encephalopathy of infancy.

Bertossi C, Cassina M, Cappellari A, Toldo I, Nosadini M, Rigon C, Suppiej A, Sartori S.

Neuropediatrics. 2015 Feb;46(1):56-64. doi: 10.1055/s-0034-1395345. Epub 2015 Jan 7. Review.

PMID:
25565401
32.

Genetics of coenzyme q10 deficiency.

Doimo M, Desbats MA, Cerqua C, Cassina M, Trevisson E, Salviati L.

Mol Syndromol. 2014 Jul;5(3-4):156-62. doi: 10.1159/000362826.

33.

A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS Locus.

Zanetti A, Tomanin R, Rampazzo A, Rigon C, Gasparotto N, Cassina M, Clementi M, Scarpa M.

JIMD Rep. 2014;17:13-21. doi: 10.1007/8904_2014_317. Epub 2014 Jul 25.

34.

First-trimester exposure to metformin and risk of birth defects: a systematic review and meta-analysis.

Cassina M, Donà M, Di Gianantonio E, Litta P, Clementi M.

Hum Reprod Update. 2014 Sep-Oct;20(5):656-69. doi: 10.1093/humupd/dmu022. Epub 2014 May 25. Review.

PMID:
24861556
35.

Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delays.

Shuvarikov A, Campbell IM, Dittwald P, Neill NJ, Bialer MG, Moore C, Wheeler PG, Wallace SE, Hannibal MC, Murray MF, Giovanni MA, Terespolsky D, Sodhi S, Cassina M, Viskochil D, Moghaddam B, Herman K, Brown CW, Beck CR, Gambin A, Cheung SW, Patel A, Lamb AN, Shaffer LG, Ellison JW, Ravnan JB, Stankiewicz P, Rosenfeld JA.

Hum Mutat. 2013 Oct;34(10):1415-23. doi: 10.1002/humu.22384. Epub 2013 Aug 13.

36.

14q12 duplication including FOXG1: is there a common age-dependent epileptic phenotype?

Bertossi C, Cassina M, De Palma L, Vecchi M, Rossato S, Toldo I, Donà M, Murgia A, Boniver C, Sartori S.

Brain Dev. 2014 May;36(5):402-7. doi: 10.1016/j.braindev.2013.06.008. Epub 2013 Jul 6. Review.

PMID:
23838309
37.

Analysis of p53 polymorphisms in individuals with multiple melanocytic nevi.

Bruson A, Zattra E, Zonta E, Cassina M, Baldo V, Clementi M, Alaibac M.

Eur J Dermatol. 2013 Apr 1;23(2):280-1. doi: 10.1684/ejd.2013.1996. No abstract available.

PMID:
23607988
38.

Pregnancy outcome in women exposed to antiepileptic drugs: teratogenic role of maternal epilepsy and its pharmacologic treatment.

Cassina M, Dilaghi A, Di Gianantonio E, Cesari E, De Santis M, Mannaioni G, Pistelli A, Clementi M.

Reprod Toxicol. 2013 Aug;39:50-7. doi: 10.1016/j.reprotox.2013.04.002. Epub 2013 Apr 13.

PMID:
23591043
39.

Eating-induced epileptic spasms in a boy with MECP2 duplication syndrome: insights into pathogenesis of genetic epilepsies.

de Palma L, Boniver C, Cassina M, Toldo I, Nosadini M, Clementi M, Sartori S.

Epileptic Disord. 2012 Dec;14(4):414-7. doi: 10.1684/epd.2012.0546.

40.

Genetic susceptibility to teratogens: state of the art.

Cassina M, Salviati L, Di Gianantonio E, Clementi M.

Reprod Toxicol. 2012 Sep;34(2):186-91. doi: 10.1016/j.reprotox.2012.05.004. Epub 2012 Jun 1. Review.

PMID:
22659091
41.

Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with SCO2 mutations.

Casarin A, Giorgi G, Pertegato V, Siviero R, Cerqua C, Doimo M, Basso G, Sacconi S, Cassina M, Rizzuto R, Brosel S, M Davidson M, Dimauro S, Schon EA, Clementi M, Trevisson E, Salviati L.

Orphanet J Rare Dis. 2012 Apr 19;7:21.

42.

Pharmacologic treatment of hyperthyroidism during pregnancy.

Cassina M, Donà M, Di Gianantonio E, Clementi M.

Birth Defects Res A Clin Mol Teratol. 2012 Aug;94(8):612-9. doi: 10.1002/bdra.23012. Epub 2012 Apr 18. Review.

PMID:
22511519
43.

Congenital pulmonary airway malformation (CPAM) [congenital cystic adenomatoid malformation] associated with tracheoesophageal fistula and agensesis of the corpus callosum.

Pizzi M, Fassan M, Ludwig K, Cassina M, Gervasi MT, Salmaso R.

Fetal Pediatr Pathol. 2012 Jun;31(3):169-75. doi: 10.3109/15513815.2012.659392. Epub 2012 Mar 13.

PMID:
22414029
44.

Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency.

Salviati L, Trevisson E, Rodriguez Hernandez MA, Casarin A, Pertegato V, Doimo M, Cassina M, Agosto C, Desbats MA, Sartori G, Sacconi S, Memo L, Zuffardi O, Artuch R, Quinzii C, Dimauro S, Hirano M, Santos-Ocaña C, Navas P.

J Med Genet. 2012 Mar;49(3):187-91. doi: 10.1136/jmedgenet-2011-100394.

45.

Pregnancy outcome in women exposed to leflunomide before or during pregnancy.

Cassina M, Johnson DL, Robinson LK, Braddock SR, Xu R, Jimenez JL, Mirrasoul N, Salas E, Luo YJ, Jones KL, Chambers CD; Organization of Teratology Information Specialists Collaborative Research Group.

Arthritis Rheum. 2012 Jul;64(7):2085-94. doi: 10.1002/art.34419.

46.

Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A.

Vecchi M, Cassina M, Casarin A, Rigon C, Drigo P, De Palma L, Clementi M.

Seizure. 2011 Dec;20(10):813-6. doi: 10.1016/j.seizure.2011.07.008. Epub 2011 Sep 3.

47.

Treatment of hyperthyroidism in pregnancy and birth defects.

Clementi M, Di Gianantonio E, Cassina M, Leoncini E, Botto LD, Mastroiacovo P; SAFE-Med Study Group.

J Clin Endocrinol Metab. 2010 Nov;95(11):E337-41. doi: 10.1210/jc.2010-0652. Epub 2010 Jul 28.

PMID:
20668039
48.

Migraine therapy during pregnancy and lactation.

Cassina M, Di Gianantonio E, Toldo I, Battistella PA, Clementi M.

Expert Opin Drug Saf. 2010 Nov;9(6):937-48. doi: 10.1517/14740338.2010.505601.

PMID:
20662551
49.

First trimester diclofenac exposure and pregnancy outcome.

Cassina M, De Santis M, Cesari E, van Eijkeren M, Berkovitch M, Eleftheriou G, Raffagnato F, Di Gianantonio E, Clementi M.

Reprod Toxicol. 2010 Nov;30(3):401-4. doi: 10.1016/j.reprotox.2010.04.010. Epub 2010 May 10.

PMID:
20438830
50.

Age estimation from the rib by components method analysis in white males.

Verzeletti A, Cassina M, Micheli L, Conti A, De Ferrari F.

Am J Forensic Med Pathol. 2010 Mar;31(1):27-33.

PMID:
20213881

Supplemental Content

Loading ...
Support Center