Martinetti M - Search Results

1

High prevalence of a screening-detected, HFE-unrelated, mild idiopathic iron overload in Northern Italy.

Barosi G, Salvaneschi L, Grasso M, Martinetti M, Marchetti M, Bodini U, Reggiani A, D'Agostino F, Nalli G, Degiuli A, De Silvestri A, Arbustini E. Barosi G, et al. Among authors: martinetti m. Haematologica. 2002 May;87(5):472-8. Haematologica. 2002. PMID: 12010659

2

The HLA alleles DRB1*13 and DQB1*06 are associated to Whipple's disease.

Martinetti M, Biagi F, Badulli C, Feurle GE, Müller C, Moos V, Schneider T, Marth T, Marchese A, Trotta L, Sachetto S, Pasi A, De Silvestri A, Salvaneschi L, Corazza GR. Martinetti M, et al. Gastroenterology. 2009 Jun;136(7):2289-94. doi: 10.1053/j.gastro.2009.01.051. Epub 2009 Jan 27. Gastroenterology. 2009. PMID: 19208355

3

Implementing non-invasive RHD genotyping on cell-free foetal DNA from maternal plasma: the Pavia experience.

Sbarsi I, Isernia P, Montanari L, Badulli C, Martinetti M, Salvaneschi L. Sbarsi I, et al. Among authors: martinetti m. Blood Transfus. 2012 Jan;10(1):34-8. doi: 10.2450/2011.0021-11. Epub 2011 Nov 16. Blood Transfus. 2012. PMID: 22153691 Free PMC article. Clinical Trial.

4

Influence of HLA-DQ2 and DQ8 on severity in celiac Disease.

Biagi F, Bianchi PI, Vattiato C, Marchese A, Trotta L, Badulli C, De Silvestri A, Martinetti M, Corazza GR. Biagi F, et al. Among authors: martinetti m. J Clin Gastroenterol. 2012 Jan;46(1):46-50. doi: 10.1097/MCG.0b013e318221077e. J Clin Gastroenterol. 2012. PMID: 21694611

5

Helicobacter pylori infection and autoimmune thyroid disease in young patients: the disadvantage of carrying the human leukocyte antigen-DRB1*0301 allele.

Larizza D, Calcaterra V, Martinetti M, Negrini R, De Silvestri A, Cisternino M, Iannone AM, Solcia E. Larizza D, et al. Among authors: martinetti m. J Clin Endocrinol Metab. 2006 Jan;91(1):176-9. doi: 10.1210/jc.2005-1272. Epub 2005 Nov 1. J Clin Endocrinol Metab. 2006. PMID: 16263823

6

Parental GM and HLA genotypes and reduced birth weight in patients with Turner's syndrome.

Larizza D, Martinetti M, Dugoujon JM, Tinelli C, Calcaterra V, Cuccia M, Salvaneschi L, Severi F. Larizza D, et al. Among authors: martinetti m. J Pediatr Endocrinol Metab. 2002 Sep-Oct;15(8):1183-90. doi: 10.1515/jpem.2002.15.8.1183. J Pediatr Endocrinol Metab. 2002. PMID: 12387517

7

Excess of activating killer cell immunoglobulin‑like receptors and lack of HLA-Bw4 ligands: a two‑edged weapon in chronic fatigue syndrome.

Pasi A, Bozzini S, Carlo-Stella N, Martinetti M, Bombardieri S, De Silvestri A, Salvaneschi L, Cuccia M. Pasi A, et al. Among authors: martinetti m. Mol Med Rep. 2011 May-Jun;4(3):535-40. doi: 10.3892/mmr.2011.447. Epub 2011 Mar 4. Mol Med Rep. 2011. PMID: 21468604

8

HLA-DQ genetics in children with celiac disease: a meta-analysis suggesting a two-step genetic screening procedure starting with HLA-DQ β chains.

De Silvestri A, Capittini C, Poddighe D, Valsecchi C, Marseglia G, Tagliacarne SC, Scotti V, Rebuffi C, Pasi A, Martinetti M, Tinelli C. De Silvestri A, et al. Among authors: martinetti m. Pediatr Res. 2018 Mar;83(3):564-572. doi: 10.1038/pr.2017.307. Epub 2018 Jan 17. Pediatr Res. 2018. PMID: 29244800

9

No evidence of autoimmunity in 6-year-old children immunized at birth with recombinant hepatitis B vaccine.

Belloni C, Avanzini MA, De Silvestri A, Martinetti M, Pasi A, Coslovich E, Autelli M, Masanti ML, Cuccia M, Tinelli C, Rondini G, Lorini R. Belloni C, et al. Among authors: martinetti m. Pediatrics. 2002 Jul;110(1 Pt 1):e4. doi: 10.1542/peds.110.1.e4. Pediatrics. 2002. PMID: 12093985

10

Complement receptor 1 gene polymorphisms are associated with idiopathic pulmonary fibrosis.

Zorzetto M, Ferrarotti I, Trisolini R, Lazzari Agli L, Scabini R, Novo M, De Silvestri A, Patelli M, Martinetti M, Cuccia M, Poletti V, Pozzi E, Luisetti M. Zorzetto M, et al. Among authors: martinetti m. Am J Respir Crit Care Med. 2003 Aug 1;168(3):330-4. doi: 10.1164/rccm.200302-221OC. Epub 2003 May 28. Am J Respir Crit Care Med. 2003. PMID: 12773320

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