Sinibaldi C - Search Results

1

Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population.

Giardina E, Novelli G, Costanzo A, Nisticò S, Bulli C, Sinibaldi C, Sorgi ML, Chimenti S, Pallone F, Taccari E, Borgiani P. Giardina E, et al. Among authors: sinibaldi c. J Invest Dermatol. 2004 May;122(5):1106-7. doi: 10.1111/j.0022-202X.2004.22524.x. J Invest Dermatol. 2004. PMID: 15140210 Free article.

2

PSORS2 markers are not associated with psoriatic arthritis in the Italian population.

Giardina E, Predazzi I, Sinibaldi C, Peconi C, Amerio P, Costanzo A, Paradisi A, Capizzi R, Paradisi M, Chimenti S, Taccari E, Novelli G. Giardina E, et al. Among authors: sinibaldi c. Hum Hered. 2006;61(2):120-2. doi: 10.1159/000093529. Epub 2006 May 30. Hum Hered. 2006. PMID: 16733365

3

The psoriasis genetics as a model of complex disease.

Giardina E, Sinibaldi C, Novelli G. Giardina E, et al. Among authors: sinibaldi c. Curr Drug Targets Inflamm Allergy. 2004 Jun;3(2):129-36. doi: 10.2174/1568010043343877. Curr Drug Targets Inflamm Allergy. 2004. PMID: 15180465 Review.

4

Mapping the future of common diseases: lessons from psoriasis.

Giardina E, Sinibaldi C, Novelli G. Giardina E, et al. Among authors: sinibaldi c. Front Biosci. 2007 Jan 1;12:1563-73. doi: 10.2741/2169. Front Biosci. 2007. PMID: 17127403 Review.

5

Co-localization of susceptibility loci for psoriasis (PSORS4) and atopic dermatitis (ATOD2) on human chromosome 1q21.

Giardina E, Sinibaldi C, Chini L, Moschese V, Marulli G, Provini A, Rossi P, Paradisi M, Chimenti S, Galli E, Brunetti E, Girolomoni G, Novelli G. Giardina E, et al. Among authors: sinibaldi c. Hum Hered. 2006;61(4):229-36. doi: 10.1159/000095059. Epub 2006 Aug 15. Hum Hered. 2006. PMID: 16912508

6

Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian population.

Ricci F, Zampatti S, D'Abbruzzi F, Missiroli F, Martone C, Lepre T, Pietrangeli I, Sinibaldi C, Peconi C, Novelli G, Giardina E. Ricci F, et al. Among authors: sinibaldi c. Arch Ophthalmol. 2009 Oct;127(10):1368-72. doi: 10.1001/archophthalmol.2009.237. Arch Ophthalmol. 2009. PMID: 19822855

7

A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15.

Giardina E, Peconi C, Cascella R, Sinibaldi C, Nardone AM, Novelli G. Giardina E, et al. Among authors: sinibaldi c. Electrophoresis. 2008 Dec;29(23):4775-9. doi: 10.1002/elps.200800047. Electrophoresis. 2008. PMID: 19053076

8

R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients.

Giardina E, Paolillo N, Sinibaldi C, Novelli G. Giardina E, et al. Among authors: sinibaldi c. Dermatology. 2008;216(1):83-4. doi: 10.1159/000109365. Dermatology. 2008. PMID: 18032906 Free article. No abstract available.

9

A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7.

Giardina E, Peconi C, Cascella R, Sinibaldi C, Foti Cuzzola V, Nardone AM, Bramanti P, Novelli G. Giardina E, et al. Among authors: sinibaldi c. Electrophoresis. 2009 Jun;30(11):2008-11. doi: 10.1002/elps.200800744. Electrophoresis. 2009. PMID: 19517448

10

Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study.

Capoluongo E, Vento G, Rocchetti S, Giardina E, Concolino P, Sinibaldi C, Santonocito C, Vendettuoli V, Tana M, Tirone C, Zuppi C, Romagnoli C, Novelli G, Giardina B, Ameglio F. Capoluongo E, et al. Among authors: sinibaldi c. Intensive Care Med. 2007 Oct;33(10):1787-94. doi: 10.1007/s00134-007-0793-x. Epub 2007 Jul 26. Intensive Care Med. 2007. PMID: 17653692

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