Booth SE - Search Results

1

Transthyretin Ile73Val is associated with familial amyloidotic polyneuropathy in a Bangladeshi family. Mutations in brief no. 158. Online.

Booth DR, Gillmore JD, Persey MR, Booth SE, Cafferty KD, Tennent GA, Madhoo S, Cochrane SW, Whitehead TC, Pasvol G, Hawkins PN. Booth DR, et al. Among authors: booth se. Hum Mutat. 1998;12(2):135. doi: 10.1002/(SICI)1098-1004(1998)12:2<135::AID-HUMU10>3.0.CO;2-6. Hum Mutat. 1998. PMID: 10694917

2

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

3

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.

4

Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.

Soutar AK, Hawkins PN, Vigushin DM, Tennent GA, Booth SE, Hutton T, Nguyen O, Totty NF, Feest TG, Hsuan JJ, et al. Soutar AK, et al. Among authors: booth se. Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7389-93. doi: 10.1073/pnas.89.16.7389. Proc Natl Acad Sci U S A. 1992. PMID: 1502149 Free PMC article.

5

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.

6

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.

7

Molecular mechanisms of fibrillogenesis and the protective role of amyloid P component: two possible avenues for therapy.

Pepys MB, Tennent GA, Booth DR, Bellotti V, Lovat LB, Tan SY, Persey MR, Hutchinson WL, Booth SE, Madhoo S, Soutar AK, Hawkins PN, Van Zyl-Smit R, Campistol JM, Fraser PE, Radford SE, Robinson CV, Sunde M, Serpell LC, Blake CC. Pepys MB, et al. Among authors: booth dr, booth se. Ciba Found Symp. 1996;199:73-81; discussion 81-9. doi: 10.1002/9780470514924.ch6. Ciba Found Symp. 1996. PMID: 8915605

8

Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I.

Persey MR, Booth DR, Booth SE, van Zyl-Smit R, Adams BK, Fattaar AB, Tennent GA, Hawkins PN, Pepys MB. Persey MR, et al. Among authors: booth dr, booth se. Kidney Int. 1998 Feb;53(2):276-81. doi: 10.1046/j.1523-1755.1998.00770.x. Kidney Int. 1998. PMID: 9461086 Free article.

9

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

10

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

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