Hawkins PN - Search Results

1

Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis.

Lachmann HJ, Booth DR, Booth SE, Bybee A, Gilbertson JA, Gillmore JD, Pepys MB, Hawkins PN. Lachmann HJ, et al. Among authors: hawkins pn. N Engl J Med. 2002 Jun 6;346(23):1786-91. doi: 10.1056/NEJMoa013354. N Engl J Med. 2002. PMID: 12050338 Free article.

2

Imaging amyloidosis in Still's disease.

Hawkins P, Bloom SR, Cassar J, Cox TM, Pepys MB, Waxman J. Hawkins P, et al. BMJ. 1989 Sep 30;299(6703):848-50. doi: 10.1136/bmj.299.6703.848. BMJ. 1989. PMID: 2510854 Free PMC article. No abstract available.

3

An Israeli Arab patient with a de novo TNFRSF1A mutation causing tumor necrosis factor receptor-associated periodic syndrome.

Aganna E, Zeharia A, Hitman GA, Basel-Vanagaite L, Allotey RA, Booth DR, Hawkins PN, Thacker C, Syndercombe-Court D, McDermott MF. Aganna E, et al. Among authors: hawkins pn. Arthritis Rheum. 2002 Jan;46(1):245-9. doi: 10.1002/1529-0131(200201)46:1<245::AID-ART10038>3.0.CO;2-6. Arthritis Rheum. 2002. PMID: 11817598 Free article.

4

Translocations of 14q32 and deletions of 13q14 are common chromosomal abnormalities in systemic amyloidosis.

Harrison CJ, Mazzullo H, Ross FM, Cheung KL, Gerrard G, Harewood L, Mehta A, Lachmann HJ, Hawkins PN, Orchard KH. Harrison CJ, et al. Among authors: hawkins pn. Br J Haematol. 2002 May;117(2):427-35. doi: 10.1046/j.1365-2141.2002.03438.x. Br J Haematol. 2002. PMID: 11972529 Free article.

5

The importance of complete screening for amyloid fibril type and systemic disease in patients with amyloidosis in the respiratory tract.

Shah PL, Gillmore JD, Copley SJ, Collins JV, Wells AU, du Bois RM, Hawkins PN, Nicholson AG. Shah PL, et al. Among authors: hawkins pn. Sarcoidosis Vasc Diffuse Lung Dis. 2002 Jun;19(2):134-42. Sarcoidosis Vasc Diffuse Lung Dis. 2002. PMID: 12102609

6

Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis.

Aganna E, Martinon F, Hawkins PN, Ross JB, Swan DC, Booth DR, Lachmann HJ, Bybee A, Gaudet R, Woo P, Feighery C, Cotter FE, Thome M, Hitman GA, Tschopp J, McDermott MF. Aganna E, et al. Among authors: hawkins pn. Arthritis Rheum. 2002 Sep;46(9):2445-52. doi: 10.1002/art.10509. Arthritis Rheum. 2002. PMID: 12355493 Free article.

7

Rapid and complete resolution of proteinuria due to renal amyloidosis in a patient with rheumatoid arthritis treated with infliximab.

Elkayam O, Hawkins PN, Lachmann H, Yaron M, Caspi D. Elkayam O, et al. Among authors: hawkins pn. Arthritis Rheum. 2002 Oct;46(10):2571-3. doi: 10.1002/art.10581. Arthritis Rheum. 2002. PMID: 12384913 Free article.

8

Serum amyloid P component scintigraphy for diagnosis and monitoring amyloidosis.

Hawkins PN. Hawkins PN. Curr Opin Nephrol Hypertens. 2002 Nov;11(6):649-55. doi: 10.1097/00041552-200211000-00013. Curr Opin Nephrol Hypertens. 2002. PMID: 12394612 Review.

9

The significance of paired MEFV mutations in individuals without symptoms of familial Mediterranean fever.

Tunca M, Akar S, Hawkins PN, Booth SE, Sengül B, Yavuzşen TU, Oktem S, Soytürk M, Akkoç N, Booth DR. Tunca M, et al. Among authors: hawkins pn. Eur J Hum Genet. 2002 Dec;10(12):786-9. doi: 10.1038/sj.ejhg.5200900. Eur J Hum Genet. 2002. PMID: 12461684

10

Interleukin-1-receptor antagonist in the Muckle-Wells syndrome.

Hawkins PN, Lachmann HJ, McDermott MF. Hawkins PN, et al. N Engl J Med. 2003 Jun 19;348(25):2583-4. doi: 10.1056/NEJM200306193482523. N Engl J Med. 2003. PMID: 12815153 Free article. No abstract available.

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