Lachmann HJ - Search Results

1

Unicentric Castleman's disease complicated by systemic AA amyloidosis: a curable disease.

Lachmann HJ, Gilbertson JA, Gillmore JD, Hawkins PN, Pepys MB. Lachmann HJ, et al. QJM. 2002 Apr;95(4):211-8. doi: 10.1093/qjmed/95.4.211. QJM. 2002. PMID: 11937647 Review.

2

The genetic basis of autosomal dominant familial Mediterranean fever.

Booth DR, Gillmore JD, Lachmann HJ, Booth SE, Bybee A, Soytürk M, Akar S, Pepys MB, Tunca M, Hawkins PN. Booth DR, et al. Among authors: lachmann hj. QJM. 2000 Apr;93(4):217-21. doi: 10.1093/qjmed/93.4.217. QJM. 2000. PMID: 10787449

3

Transthyretin Ala97Ser is associated with familial amyloidotic polyneuropathy in a Chinese-Taiwanese family.

Lachmann HJ, Booth DR, Bybee A, Hawkins PN. Lachmann HJ, et al. Hum Mutat. 2000 Aug;16(2):180. doi: 10.1002/1098-1004(200008)16:2<180::AID-HUMU19>3.0.CO;2-A. Hum Mutat. 2000. PMID: 10923048 No abstract available.

4

Prevalence and significance of the familial Mediterranean fever gene mutation encoding pyrin Q148.

Booth DR, Lachmann HJ, Gillmore JD, Booth SE, Hawkins PN. Booth DR, et al. Among authors: lachmann hj. QJM. 2001 Oct;94(10):527-31. doi: 10.1093/qjmed/94.10.527. QJM. 2001. PMID: 11588211

5

Targeted pharmacological depletion of serum amyloid P component for treatment of human amyloidosis.

Pepys MB, Herbert J, Hutchinson WL, Tennent GA, Lachmann HJ, Gallimore JR, Lovat LB, Bartfai T, Alanine A, Hertel C, Hoffmann T, Jakob-Roetne R, Norcross RD, Kemp JA, Yamamura K, Suzuki M, Taylor GW, Murray S, Thompson D, Purvis A, Kolstoe S, Wood SP, Hawkins PN. Pepys MB, et al. Among authors: lachmann hj. Nature. 2002 May 16;417(6886):254-9. doi: 10.1038/417254a. Nature. 2002. PMID: 12015594

6

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. Arthritis Rheum. 2002 Oct;46(10):2571-3. doi: 10.1002/art.10581. Arthritis Rheum. 2002. PMID: 12384913 Free article.

7

Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosis.

Aganna E, Hawkins PN, Ozen S, Pettersson T, Bybee A, McKee SA, Lachmann HJ, Karenko L, Ranki A, Bakkaloglu A, Besbas N, Topaloglu R, Hoffman HM, Hitman GA, Woo P, McDermott MF. Aganna E, et al. Among authors: lachmann hj. Genes Immun. 2004 Jun;5(4):289-93. doi: 10.1038/sj.gene.6364070. Genes Immun. 2004. PMID: 15071491

8

Case report: Response in proteinuria due to AA amyloidosis but not Felty's syndrome in a patient with rheumatoid arthritis treated with TNF-alpha blockade.

Ravindran J, Shenker N, Bhalla AK, Lachmann H, Hawkins P. Ravindran J, et al. Rheumatology (Oxford). 2004 May;43(5):669-72. doi: 10.1093/rheumatology/keh128. Rheumatology (Oxford). 2004. PMID: 15103032 No abstract available.

9

Colchicine responsive periodic fever syndrome associated with pyrin I591T.

Fisher BA, Lachmann HJ, Rowczenio D, Goodman HJ, Bhalara S, Hawkins PN. Fisher BA, et al. Among authors: lachmann hj. Ann Rheum Dis. 2005 Sep;64(9):1384-5. doi: 10.1136/ard.2004.030379. Ann Rheum Dis. 2005. PMID: 16100353 Free PMC article. No abstract available.

10

Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations.

Lachmann HJ, Sengül B, Yavuzşen TU, Booth DR, Booth SE, Bybee A, Gallimore JR, Soytürk M, Akar S, Tunca M, Hawkins PN. Lachmann HJ, et al. Rheumatology (Oxford). 2006 Jun;45(6):746-50. doi: 10.1093/rheumatology/kei279. Epub 2006 Jan 10. Rheumatology (Oxford). 2006. PMID: 16403826

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