Porfirio B - Search Results

1

MICA gene polymorphisms in an Italian paediatric series of juvenile Behçet disease.

Picco P, Porfirio B, Gattorno M, Buoncompagni A, Falcini F, Cusano R, Bordo D, Pistoia V, Ravazzolo R, Seri M. Picco P, et al. Among authors: porfirio b. Int J Mol Med. 2002 Nov;10(5):575-8. Int J Mol Med. 2002. PMID: 12373294

2

Juvenile dermatomyositis and celiac disease.

Falcini F, Porfirio B, Lionetti P. Falcini F, et al. Among authors: porfirio b. J Rheumatol. 1999 Jun;26(6):1419-20. J Rheumatol. 1999. PMID: 10381073 No abstract available.

3

Lack of association between the HLA-DRB1 locus and post-streptococcal reactive arthritis and acute rheumatic fever in Italian children.

Simonini G, Porfirio B, Cimaz R, Calabri GB, Giani T, Falcini F. Simonini G, et al. Among authors: porfirio b. Semin Arthritis Rheum. 2004 Oct;34(2):553-8. doi: 10.1016/j.semarthrit.2004.04.001. Semin Arthritis Rheum. 2004. PMID: 15505772

4

Alpha-actin gene mutations and polymorphisms in Italian patients with nemaline myopathy.

Graziano C, Bertini E, Minetti C, Porfirio B. Graziano C, et al. Among authors: porfirio b. Int J Mol Med. 2004 Jun;13(6):805-9. Int J Mol Med. 2004. PMID: 15138616

5

Variable response to the diepoxybutane test in two dizygotic twins with Fanconi's anemia and flow cytometry for diagnosis confirmation.

Toraldo R, Canino G, Tolone C, D'Avanzo M, Porfirio B, Hoehn H, Schroeder-Kurth T, Pistoia V. Toraldo R, et al. Among authors: porfirio b. Pediatr Hematol Oncol. 1998 Jan-Feb;15(1):45-54. doi: 10.3109/08880019809009507. Pediatr Hematol Oncol. 1998. PMID: 9509505

6

A method for point mutation analysis that links SSCP and dye primer fluorescent sequencing.

Chiarelli I, Porfirio B, Mattiuz PL, Seri M, Caroli F, Celli I, Romeo G, Volorio S, Zollo M. Chiarelli I, et al. Among authors: porfirio b. Mol Cell Probes. 1998 Jun;12(3):125-31. doi: 10.1006/mcpr.1998.0159. Mol Cell Probes. 1998. PMID: 9664573

7

Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy.

Wallgren-Pettersson C, Pelin K, Hilpelä P, Donner K, Porfirio B, Graziano C, Swoboda KJ, Fardeau M, Urtizberea JA, Muntoni F, Sewry C, Dubowitz V, Iannaccone S, Minetti C, Pedemonte M, Seri M, Cusano R, Lammens M, Castagna-Sloane A, Beggs AH, Laing NG, de la Chapelle A. Wallgren-Pettersson C, et al. Among authors: porfirio b. Neuromuscul Disord. 1999 Dec;9(8):564-72. doi: 10.1016/s0960-8966(99)00061-9. Neuromuscul Disord. 1999. PMID: 10619714

8

HLA-B44 subtypes and the chance of finding HLA compatible donor/recipient pairs for bone marrow transplantation: a haplotype study of 303 Italian families.

Mattiuz PL, Di Paolo E, Fossombroni V, Menicucci A, Pradella F, Porfirio B, Rombolà G. Mattiuz PL, et al. Among authors: porfirio b. Tissue Antigens. 1997 Dec;50(6):602-9. doi: 10.1111/j.1399-0039.1997.tb02918.x. Tissue Antigens. 1997. PMID: 9458113

9

Functional polymorphisms of the microsomal epoxide hydrolase gene: a reappraisal on a early-onset lung cancer patients series.

Graziano C, Comin CE, Crisci C, Novelli L, Politi L, Messerini L, Andreani M, Porfirio B. Graziano C, et al. Among authors: porfirio b. Lung Cancer. 2009 Feb;63(2):187-93. doi: 10.1016/j.lungcan.2008.05.004. Epub 2008 Jun 20. Lung Cancer. 2009. PMID: 18571762

10

Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation.

D'Amico A, Graziano C, Pacileo G, Petrini S, Nowak KJ, Boldrini R, Jacques A, Feng JJ, Porfirio B, Sewry CA, Santorelli FM, Limongelli G, Bertini E, Laing N, Marston SB. D'Amico A, et al. Among authors: porfirio b. Neuromuscul Disord. 2006 Oct;16(9-10):548-52. doi: 10.1016/j.nmd.2006.07.005. Epub 2006 Sep 1. Neuromuscul Disord. 2006. PMID: 16945537

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