Booth SE - Search Results

1

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: booth se. QJM. 2001 Oct;94(10):527-31. doi: 10.1093/qjmed/94.10.527. QJM. 2001. PMID: 11588211

2

Pyrin/marenostrin mutations in familial Mediterranean fever.

Booth DR, Gillmore JD, Booth SE, Pepys MB, Hawkins PN. Booth DR, et al. Among authors: booth se. QJM. 1998 Sep;91(9):603-6. doi: 10.1093/qjmed/91.9.603. QJM. 1998. PMID: 10024914

3

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: booth se. QJM. 2000 Apr;93(4):217-21. doi: 10.1093/qjmed/93.4.217. QJM. 2000. PMID: 10787449

4

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. Among authors: booth se. Rheumatology (Oxford). 2006 Jun;45(6):746-50. doi: 10.1093/rheumatology/kei279. Epub 2006 Jan 10. Rheumatology (Oxford). 2006. PMID: 16403826

5

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: booth se. N Engl J Med. 2002 Jun 6;346(23):1786-91. doi: 10.1056/NEJMoa013354. N Engl J Med. 2002. PMID: 12050338 Free article.

6

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: booth se. Eur J Hum Genet. 2002 Dec;10(12):786-9. doi: 10.1038/sj.ejhg.5200900. Eur J Hum Genet. 2002. PMID: 12461684

7

A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosis.

Booth DR, Tan SY, Booth SE, Hsuan JJ, Totty NF, Nguyen O, Hutton T, Vigushin DM, Tennent GA, Hutchinson WL, et al. Booth DR, et al. Among authors: booth se. QJM. 1995 Oct;88(10):695-702. QJM. 1995. PMID: 7493166 Review.

8

Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene.

Booth DR, Tan SY, Booth SE, Tennent GA, Hutchinson WL, Hsuan JJ, Totty NF, Truong O, Soutar AK, Hawkins PN, Bruguera M, Caballería J, Solé M, Campistol JM, Pepys MB. Booth DR, et al. Among authors: booth se. J Clin Invest. 1996 Jun 15;97(12):2714-21. doi: 10.1172/JCI118725. J Clin Invest. 1996. PMID: 8675681 Free PMC article.

9

SAA1 alleles as risk factors in reactive systemic AA amyloidosis.

Booth DR, Booth SE, Gillmore JD, Hawkins PN, Pepys MB. Booth DR, et al. Among authors: booth se. Amyloid. 1998 Dec;5(4):262-5. doi: 10.3109/13506129809007299. Amyloid. 1998. PMID: 10036584

10

Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis.

Brett M, Persey MR, Reilly MM, Revesz T, Booth DR, Booth SE, Hawkins PN, Pepys MB, Morgan-Hughes JA. Brett M, et al. Among authors: booth dr, booth se. Brain. 1999 Feb;122 ( Pt 2):183-90. doi: 10.1093/brain/122.2.183. Brain. 1999. PMID: 10071047

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