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Items: 6

1.

From structure to function for the characterization of ERAP1 active site in Behçet syndrome. A novel polymorphism associated with known gene variations.

Padula MC, Leccese P, Lascaro N, Carbone T, Limongi AR, Radice RP, Padula AA, D'Angelo S, Martelli G.

Mol Immunol. 2020 Jan;117:155-159. doi: 10.1016/j.molimm.2019.11.005. Epub 2019 Nov 29.

PMID:
31790864
2.

Real-world effectiveness of apremilast in multirefractory mucosal involvement of Behçet's disease.

Lopalco G, Venerito V, Leccese P, Emmi G, Cantarini L, Lascaro N, Di Scala G, Fabiani C, Rigante D, Iannone F.

Ann Rheum Dis. 2019 Dec;78(12):1736-1737. doi: 10.1136/annrheumdis-2019-215437. Epub 2019 Aug 10. No abstract available.

PMID:
31401548
3.

Identification of a de novo NLRP3 gene variation in an Italian Behçet syndrome patient.

Padula MC, Leccese P, Lascaro N, Padula AA, Carbone T, Martelli G, D'Angelo S.

Int J Immunogenet. 2019 Oct;46(5):339-341. doi: 10.1111/iji.12442. Epub 2019 Jun 10.

PMID:
31183983
4.

HLA-B*51 subtypes molecular analysis in a series of Italian patients with Behçet's syndrome.

Leccese P, Padula MC, Santospirito EV, Colucci R, Lascaro N, D'Angelo S.

Joint Bone Spine. 2019 Nov;86(6):807-808. doi: 10.1016/j.jbspin.2019.04.011. Epub 2019 May 5. No abstract available.

PMID:
31067502
5.

Distribution of rs17482078 and rs27044 ERAP1 polymorphisms in a group of Italian Behçet's syndrome patients: a preliminary case-control study.

Padula MC, Leccese P, Pellizzieri E, Padula AA, Gilio M, Carbone T, Lascaro N, Tramontano G, Martelli G, D'Angelo S.

Intern Emerg Med. 2019 Aug;14(5):713-718. doi: 10.1007/s11739-019-02056-w. Epub 2019 Feb 28.

PMID:
30820838
6.

Genotyping of Italian patients with Behçet syndrome identified two novel ERAP1 polymorphisms using sequencing-based approach.

Padula MC, Leccese P, Lascaro N, Carbone T, Gilio M, Padula AA, Martelli G, D'Angelo S.

Hum Immunol. 2019 May;80(5):335-338. doi: 10.1016/j.humimm.2019.02.003. Epub 2019 Feb 8.

PMID:
30742879

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