Hawkins PN - Search Results

1

Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain gene.

Kang HG, Bybee A, Ha IS, Park MS, Gilbertson JA, Cheong HI, Choi Y, Hawkins PN. Kang HG, et al. Among authors: hawkins pn. Kidney Int. 2005 Nov;68(5):1994-8. doi: 10.1111/j.1523-1755.2005.00653.x. Kidney Int. 2005. PMID: 16221199 Free article.

2

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.

3

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.

4

Familial amyloidotic polyneuropathy with severe renal involvement in association with transthyretin Gly47Glu in Dutch, British and American-Finnish families.

Haagsma EB, Hawkins PN, Benson MD, Lachmann HJ, Bybee A, Hazenberg BP. Haagsma EB, et al. Among authors: hawkins pn. Amyloid. 2004 Mar;11(1):44-9. doi: 10.1080/13506120410001682578. Amyloid. 2004. PMID: 15185498

5

Response to anakinra in a de novo case of neonatal-onset multisystem inflammatory disease.

Hawkins PN, Bybee A, Aganna E, McDermott MF. Hawkins PN, et al. Arthritis Rheum. 2004 Aug;50(8):2708-9. doi: 10.1002/art.20357. Arthritis Rheum. 2004. PMID: 15334488 Free article. No abstract available.

6

AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: a report of two cases.

Lachmann HJ, Goodman HJ, Andrews PA, Gallagher H, Marsh J, Breuer S, Rowczenio DM, Bybee A, Hawkins PN. Lachmann HJ, et al. Among authors: hawkins pn. Arthritis Rheum. 2006 Jun;54(6):2010-4. doi: 10.1002/art.21901. Arthritis Rheum. 2006. PMID: 16732551 Free article.

7

Phenotype, genotype, and sustained response to anakinra in 22 patients with autoinflammatory disease associated with CIAS-1/NALP3 mutations.

Leslie KS, Lachmann HJ, Bruning E, McGrath JA, Bybee A, Gallimore JR, Roberts PF, Woo P, Grattan CE, Hawkins PN. Leslie KS, et al. Among authors: hawkins pn. Arch Dermatol. 2006 Dec;142(12):1591-7. doi: 10.1001/archderm.142.12.1591. Arch Dermatol. 2006. PMID: 17178985

8

Natural history and outcome in systemic AA amyloidosis.

Lachmann HJ, Goodman HJ, Gilbertson JA, Gallimore JR, Sabin CA, Gillmore JD, Hawkins PN. Lachmann HJ, et al. Among authors: hawkins pn. N Engl J Med. 2007 Jun 7;356(23):2361-71. doi: 10.1056/NEJMoa070265. N Engl J Med. 2007. PMID: 17554117 Free article.

9

Diagnosis, pathogenesis, treatment, and prognosis of hereditary fibrinogen A alpha-chain amyloidosis.

Gillmore JD, Lachmann HJ, Rowczenio D, Gilbertson JA, Zeng CH, Liu ZH, Li LS, Wechalekar A, Hawkins PN. Gillmore JD, et al. Among authors: hawkins pn. J Am Soc Nephrol. 2009 Feb;20(2):444-51. doi: 10.1681/ASN.2008060614. Epub 2008 Dec 10. J Am Soc Nephrol. 2009. PMID: 19073821 Free PMC article.

10

Laryngeal presentation of systemic apolipoprotein A-I-derived amyloidosis.

Hazenberg AJ, Dikkers FG, Hawkins PN, Bijzet J, Rowczenio D, Gilbertson J, Posthumus MD, Leijsma MK, Hazenberg BP. Hazenberg AJ, et al. Among authors: hawkins pn. Laryngoscope. 2009 Mar;119(3):608-15. doi: 10.1002/lary.20106. Laryngoscope. 2009. PMID: 19235761

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