Booth DR - Search Results

1

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. Among authors: booth dr. 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.

2

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

3

A novel variant of human lysozyme (T70N) is common in the normal population.

Booth DR, Pepys MB, Hawkins PN. Booth DR, et al. Hum Mutat. 2000 Aug;16(2):180. doi: 10.1002/1098-1004(200008)16:2<180::AID-HUMU20>3.0.CO;2-#. Hum Mutat. 2000. PMID: 10923049 No abstract available.

4

Transthyretin Ile84Thr is associated with familial amyloid polyneuropathy.

Booth DR, Stangou A, Williams RS, Gillmore JD, Tennent GA, Hawkins PN. Booth DR, et al. Hum Mutat. 2000 Nov;16(5):447. doi: 10.1002/1098-1004(200011)16:5<447::AID-HUMU16>3.0.CO;2-P. Hum Mutat. 2000. PMID: 11058909 No abstract available.

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 dr, 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

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

7

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

8

Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26Arg.

Gillmore JD, Stangou AJ, Tennent GA, Booth DR, O'Grady J, Rela M, Heaton ND, Wall CA, Keogh JA, Hawkins PN. Gillmore JD, et al. Among authors: booth dr. Transplantation. 2001 Apr 15;71(7):986-92. doi: 10.1097/00007890-200104150-00026. Transplantation. 2001. PMID: 11349736

9

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

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. Among authors: booth dr, booth se. 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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