Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 14

1.

Strategies for multivessel revascularization in patients with diabetes.

Farkouh ME, Domanski M, Sleeper LA, Siami FS, Dangas G, Mack M, Yang M, Cohen DJ, Rosenberg Y, Solomon SD, Desai AS, Gersh BJ, Magnuson EA, Lansky A, Boineau R, Weinberger J, Ramanathan K, Sousa JE, Rankin J, Bhargava B, Buse J, Hueb W, Smith CR, Muratov V, Bansilal S, King S 3rd, Bertrand M, Fuster V; FREEDOM Trial Investigators..

N Engl J Med. 2012 Dec 20;367(25):2375-84. doi: 10.1056/NEJMoa1211585. Epub 2012 Nov 4.

2.

Radial versus femoral access for coronary angiography and intervention in patients with acute coronary syndromes (RIVAL): a randomised, parallel group, multicentre trial.

Jolly SS, Yusuf S, Cairns J, Niemelä K, Xavier D, Widimsky P, Budaj A, Niemelä M, Valentin V, Lewis BS, Avezum A, Steg PG, Rao SV, Gao P, Afzal R, Joyner CD, Chrolavicius S, Mehta SR; RIVAL trial group..

Lancet. 2011 Apr 23;377(9775):1409-20. doi: 10.1016/S0140-6736(11)60404-2. Epub 2011 Apr 4. Erratum in: Lancet. 2011 Apr 23;377(9775):1408. Lancet. 2011 Jul 2;378(9785):30.

PMID:
21470671
3.

Emergency coronary artery bypass surgery in the era of glycoprotein IIb/IIIa receptor antagonist use.

Pang JT, Fort S, Della Siega A, Cohen EA.

J Card Surg. 2002 Sep-Oct;17(5):425-31.

PMID:
12630543
4.

Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases.

Pang JT, Giunti P, Chamberlain S, An SF, Vitaliani R, Scaravilli T, Martinian L, Wood NW, Scaravilli F, Ansorge O.

Brain. 2002 Mar;125(Pt 3):656-63.

PMID:
11872620
5.

Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36.

Williamson C, Pannett AA, Pang JT, Wooding C, McCarthy M, Sheppard MN, Monson J, Clayton RN, Thakker RV.

J Med Genet. 1997 Aug;34(8):617-9.

6.

Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneity.

Gertner JM, Whyte MP, Dixon PH, Pang JT, Trump D, Pearce SH, Wooding C, Thakker RV.

J Bone Miner Res. 1997 Aug;12(8):1204-9.

7.

Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).

Lloyd SE, Pang JT, Pearce SH, Leigh SE, Thakker RV.

Hum Genet. 1997 May;99(5):585-9.

PMID:
9150722
8.

Clinical studies of multiple endocrine neoplasia type 1 (MEN1)

Trump D, Farren B, Wooding C, Pang JT, Besser GM, Buchanan KD, Edwards CR, Heath DA, Jackson CE, Jansen S, Lips K, Monson JP, O'Halloran D, Sampson J, Shalet SM, Wheeler MH, Zink A, Thakker RV.

QJM. 1996 Sep;89(9):653-69. Erratum in: QJM 1996 Dec;89(12):957-8.

PMID:
8917740
9.

Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene.

Pang JT, Lloyd SE, Wooding C, Farren B, Pottinger B, Harding B, Leigh SE, Pook MA, Benham FJ, Gillett GT, Taggart RT, Thakker RV.

Hum Genet. 1996 Jun;97(6):732-41.

PMID:
8641689
11.

Multiple endocrine neoplasia type 1 (MEN1).

Pang JT, Thakker RV.

Eur J Cancer. 1994;30A(13):1961-8. Review. No abstract available.

PMID:
7734208
12.

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.

Scheinman SJ, Pook MA, Wooding C, Pang JT, Frymoyer PA, Thakker RV.

J Clin Invest. 1993 Jun;91(6):2351-7.

13.

Linkage analysis of 7 polymorphic markers at chromosome 11p11.2-11q13 in 27 multiple endocrine neoplasia type 1 families.

Thakker RV, Wooding C, Pang JT, Farren B, Harding B, Anderson DC, Besser GM, Bouloux P, Brenton DP, Buchanan KD, et al.

Ann Hum Genet. 1993 Jan;57(Pt 1):17-25.

PMID:
8101435
14.

Molecular genetic mapping of the multiple endocrine neoplasia type 1 locus.

Pang JT, Pook MA, Eubanks JH, Jones C, van Heyningen V, Evans GA, Thakker RV.

Henry Ford Hosp Med J. 1992;40(3-4):162-6.

PMID:
1362397

Supplemental Content

Loading ...
Support Center