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1
Two SNPs in NLRP3 gene are involved in the predisposition to type-1 diabetes and celiac disease in a pediatric population from northeast Brazil
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Two SNPs in NLRP3 gene are involved in the predisposition to type-1 diabetes and celiac disease in a pediatric population from northeast Brazil

Pontillo, A. ; Brandao, L. ; Guimaraes, R. ; Segat, L. ; Araujo, J. ; Crovella, S.

Autoimmunity (Chur, Switzerland), 2010-12, Vol.43 (8), p.583-589 [Periódico revisado por pares]

England: Informa Healthcare

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2
Pleural mesothelioma and lung cancer: the role of asbestos exposure and genetic variants in selected iron metabolism and inflammation genes
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Artigo
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Pleural mesothelioma and lung cancer: the role of asbestos exposure and genetic variants in selected iron metabolism and inflammation genes

Celsi, F. ; Crovella, S. ; Moura, R. R. ; Schneider, M. ; Vita, F. ; Finotto, L. ; Zabucchi, G. ; Zacchi, P. ; Borelli, V.

Journal of Toxicology and Environmental Health, Part A, 2019-10, Vol.82 (20), p.1088-1102 [Periódico revisado por pares]

England: Taylor & Francis

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3
LTF and DEFB1 polymorphisms are associated with susceptibility toward chronic periodontitis development
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LTF and DEFB1 polymorphisms are associated with susceptibility toward chronic periodontitis development

Zupin, L ; Robino, A ; Navarra, CO ; Pirastu, N ; Di Lenarda, R ; Gasparini, P ; Crovella, S ; Bevilacqua, L

Oral diseases, 2017-10, Vol.23 (7), p.1001-1008 [Periódico revisado por pares]

Denmark: Wiley Subscription Services, Inc

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4
IBD and IBD mimicking enterocolitis in children younger than 2 years of age
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Artigo
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IBD and IBD mimicking enterocolitis in children younger than 2 years of age

Cannioto, Z. ; Berti, I. ; Martelossi, S. ; Bruno, I. ; Giurici, N. ; Crovella, S. ; Ventura, A.

European journal of pediatrics, 2009-02, Vol.168 (2), p.149-155 [Periódico revisado por pares]

Berlin/Heidelberg: Springer-Verlag

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5
HLA‐G regulatory polymorphisms are associated with susceptibility to HCV infection
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Artigo
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HLA‐G regulatory polymorphisms are associated with susceptibility to HCV infection

Catamo, E. ; Zupin, L. ; Freato, N. ; Polesello, V. ; Celsi, F. ; Crocè, S. L. ; Masutti, F. ; Pozzato, G. ; Segat, L. ; Crovella, S.

HLA : immune response genetics, 2017-03, Vol.89 (3), p.135-142 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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6
A genetic variant of NLRP1 gene is associated with asbestos body burden in patients with malignant pleural mesothelioma
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Artigo
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A genetic variant of NLRP1 gene is associated with asbestos body burden in patients with malignant pleural mesothelioma

Crovella, S. ; Moura, RR ; Cappellani, S. ; Celsi, F. ; Trevisan, E. ; Schneider, M. ; Brollo, A. ; Nicastro, EM ; Vita, F. ; Finotto, L. ; Zabucchi, G. ; Borelli, V.

Journal of Toxicology and Environmental Health, Part A, 2018-01, Vol.81 (5), p.98-105 [Periódico revisado por pares]

England: Taylor & Francis

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7
PIN1 promoter polymorphisms are associated with Alzheimer's disease
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Artigo
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PIN1 promoter polymorphisms are associated with Alzheimer's disease

Segat, L ; Pontillo, A ; Annoni, G ; Trabattoni, D ; Vergani, C ; Clerici, M ; Arosio, B ; Crovella, S

Neurobiology of aging, 2007-01, Vol.28 (1), p.69-74 [Periódico revisado por pares]

London: Elsevier Inc

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8
Clinical and genetic characterization of Italian patients affected by CINCA syndrome
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Artigo
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Clinical and genetic characterization of Italian patients affected by CINCA syndrome

Caroli, F ; Pontillo, A ; D'Osualdo, A ; Travan, L ; Ceccherini, I ; Crovella, S ; Alessio, M ; Stabile, A ; Gattorno, M ; Tommasini, A ; Martini, A ; Lepore, L

Rheumatology (Oxford, England), 2007-03, Vol.46 (3), p.473-478 [Periódico revisado por pares]

Oxford: Oxford University Press

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9
Mass screening for coeliac disease using antihuman transglutaminase antibody assay
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Artigo
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Mass screening for coeliac disease using antihuman transglutaminase antibody assay

Tommasini, A ; Not, T ; Kiren, V ; Baldas, V ; Santon, D ; Trevisiol, C ; Berti, I ; Neri, E ; Gerarduzzi, T ; Bruno, I ; Lenhardt, A ; Zamuner, E ; Spanò, A ; Crovella, S ; Martellossi, S ; Torre, G ; Sblattero, D ; Marzari, R ; Bradbury, A ; Tamburlini, G ; Ventura, A

Archives of disease in childhood, 2004-06, Vol.89 (6), p.512-515 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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10
A genetic variant within SLC30A6 has a protective role in the severity of rheumatoid arthritis
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A genetic variant within SLC30A6 has a protective role in the severity of rheumatoid arthritis

Adelino, JE ; Addobbati, C ; Pontillo, A ; Fragoso, TS ; Duarte, ÂLBP ; Crovella, S ; De Azevedo Silva, J ; Sandrin-Garcia, P

Scandinavian journal of rheumatology, 2017-07, Vol.46 (4), p.326-327 [Periódico revisado por pares]

England: Taylor & Francis

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