Gillmore JD - Search Results

1

Association of the transthyretin variant V122I with polyneuropathy among individuals of African ancestry.

Parker MM, Damrauer SM, Tcheandjieu C, Erbe D, Aldinc E, Hawkins PN, Gillmore JD, Hull LE, Lynch JA, Joseph J, Ticau S, Flynn-Carroll AO, Deaton AM, Ward LD, Assimes TL, Tsao PS, Chang KM, Rader DJ, Fitzgerald K, Vaishnaw AK, Hinkle G, Nioi P. Parker MM, et al. Among authors: gillmore jd. Sci Rep. 2021 Jun 2;11(1):11645. doi: 10.1038/s41598-021-91113-6. Sci Rep. 2021. PMID: 34079032 Free PMC article.

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 cardiac amyloidosis associated with the transthyretin Ile122 mutation in a white man.

Gillmore JD, Booth DR, Pepys MB, Hawkins PN. Gillmore JD, et al. Heart. 1999 Sep;82(3):e2. doi: 10.1136/hrt.82.3.e2. Heart. 1999. PMID: 10455100 Free PMC article.

7

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

8

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: gillmore jd. 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

9

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

10

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

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