Gillmore JD - Search Results

1

Molecular genetic investigation, clinical features, and response to treatment in 21 patients with Schnitzler syndrome.

Rowczenio DM, Pathak S, Arostegui JI, Mensa-Vilaro A, Omoyinmi E, Brogan P, Lipsker D, Scambler T, Owen R, Trojer H, Baginska A, Gillmore JD, Wechalekar AD, Lane T, Williams R, Youngstein T, Hawkins PN, Savic S, Lachmann HJ. Rowczenio DM, et al. Among authors: gillmore jd. Blood. 2018 Mar 1;131(9):974-981. doi: 10.1182/blood-2017-10-810366. Epub 2017 Dec 28. Blood. 2018. PMID: 29284595 Free PMC article. Clinical Trial.

2

Amyloidosis: a review of recent diagnostic and therapeutic developments.

Gillmore JD, Hawkins PN, Pepys MB. Gillmore JD, et al. Br J Haematol. 1997 Nov;99(2):245-56. doi: 10.1046/j.1365-2141.1997.303194.x. Br J Haematol. 1997. PMID: 9375734 Free article. Review.

3

Pyrin/marenostrin mutations in familial Mediterranean fever.

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

4

Amyloidosis and the respiratory tract.

Gillmore JD, Hawkins PN. Gillmore JD, et al. Thorax. 1999 May;54(5):444-51. doi: 10.1136/thx.54.5.444. Thorax. 1999. PMID: 10212113 Free PMC article. Review. No abstract available.

5

Amyloidosis and the liver.

Gillmore JD, Lovat LB, Hawkins PN. Gillmore JD, et al. J Hepatol. 1999;30 Suppl 1:17-33. J Hepatol. 1999. PMID: 10370897 Review. No abstract available.

6

Hereditary renal amyloidosis associated with variant lysozyme in a large English family.

Gillmore JD, Booth DR, Madhoo S, Pepys MB, Hawkins PN. Gillmore JD, et al. Nephrol Dial Transplant. 1999 Nov;14(11):2639-44. doi: 10.1093/ndt/14.11.2639. Nephrol Dial Transplant. 1999. PMID: 10534505

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

8

Curative hepatorenal transplantation in systemic amyloidosis caused by the Glu526Val fibrinogen alpha-chain variant in an English family.

Gillmore JD, Booth DR, Rela M, Heaton ND, Rahman V, Stangou AJ, Pepys MB, Hawkins PN. Gillmore JD, et al. QJM. 2000 May;93(5):269-75. doi: 10.1093/qjmed/93.5.269. QJM. 2000. PMID: 10825402

9

Bleeding symptoms and coagulation abnormalities in 337 patients with AL-amyloidosis.

Mumford AD, O'Donnell J, Gillmore JD, Manning RA, Hawkins PN, Laffan M. Mumford AD, et al. Among authors: gillmore jd. Br J Haematol. 2000 Aug;110(2):454-60. doi: 10.1046/j.1365-2141.2000.02183.x. Br J Haematol. 2000. PMID: 10971408 Free article.

10

Tissue Doppler features of cardiac amyloidosis.

Elliott PM, Mahon NG, Matsumura Y, Hawkins PN, Gillmore JD, McKenna WJ. Elliott PM, et al. Among authors: gillmore jd. Clin Cardiol. 2000 Sep;23(9):701. doi: 10.1002/clc.4960230913. Clin Cardiol. 2000. PMID: 11016022 Free PMC article. No abstract available.

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