-
1
-
-
59549105095
-
Cardiac manifestations of HIV infection - The African perspective
-
10.1038/ncpcardio1437 19104517
-
Ntsekhe M Mayosi BM Cardiac manifestations of HIV infection - the African perspective Nat Clin Pract Cardiovasc Med 2009, 6:120-127. 10.1038/ncpcardio1437 19104517
-
(2009)
Nat Clin Pract Cardiovasc Med
, vol.6
, pp. 120-127
-
-
Ntsekhe, M.1
Mayosi, B.M.2
-
2
-
-
33846072609
-
Prevalence of dilated cardiomyopathy in HIV-infected African patients not receiving HAART: A multicenter, observational, prospective, cohort study in Rwanda
-
10.2174/157016207779316288 17266564
-
Twagirumukiza M Nkeramihigo E Seminega B Gasakure E Boccara F Barbaro G Prevalence of dilated cardiomyopathy in HIV-infected African patients not receiving HAART: A multicenter, observational, prospective, cohort study in Rwanda Curr HIV Res 2007, 5:129-137. 10.2174/157016207779316288 17266564
-
(2007)
Curr HIV Res
, vol.5
, pp. 129-137
-
-
Twagirumukiza, M.1
Nkeramihigo, E.2
Seminega, B.3
Gasakure, E.4
Boccara, F.5
Barbaro, G.6
-
3
-
-
0032531936
-
Dilated Cardiomyopathy in HIV-Infected Patients
-
10.1056/NEJM199810153391609 9770563
-
Lipshultz SE Dilated Cardiomyopathy in HIV-Infected Patients N Engl J Med 1998, 339(16):1153-1155. 10.1056/NEJM199810153391609 9770563
-
(1998)
N Engl J Med
, vol.339
, Issue.16
, pp. 1153-1155
-
-
Lipshultz, S.E.1
-
5
-
-
0033981680
-
Mitochondrial defects in cardiomyopathy and neuromuscular disease
-
10.1067/mhj.2000.103934 10650320
-
Wallace DC Mitochondrial defects in cardiomyopathy and neuromuscular disease Am Heart J 2000, 139:S70-S85. 10.1067/mhj.2000.103934 10650320
-
(2000)
Am Heart J
, vol.139
-
-
Wallace, D.C.1
-
6
-
-
0035925906
-
A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations
-
10.1016/S0140-6736(00)04422-6 11418155
-
Khogali SS Mayosi BM Beattie JM McKenna WJ Watkins H Poulton J A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations Lancet 2001, 357:1265-1267. 10.1016/S0140-6736(00)04422-6 11418155
-
(2001)
Lancet
, vol.357
, pp. 1265-1267
-
-
Khogali, S.S.1
Mayosi, B.M.2
Beattie, J.M.3
McKenna, W.J.4
Watkins, H.5
Poulton, J.6
-
7
-
-
20444428352
-
A bidirectional origin of replication maps to the major noncoding region of human mitochondrial DNA
-
10.1016/j.molcel.2005.05.002 15949440
-
Yasukawa T Yang MY Jacobs HT Holt IJ A bidirectional origin of replication maps to the major noncoding region of human mitochondrial DNA Mol Cell 2005, 18:651-662. 10.1016/j.molcel.2005.05.002 15949440
-
(2005)
Mol Cell
, vol.18
, pp. 651-662
-
-
Yasukawa, T.1
Yang, M.Y.2
Jacobs, H.T.3
Holt, I.J.4
-
8
-
-
15644370476
-
A common mitochondrial DNA variant is associated with insulin resistance in adult life
-
10.1007/s001250050866 9498630
-
Poulton J Brown MS Cooper A Marchington DR Phillips DI A common mitochondrial DNA variant is associated with insulin resistance in adult life Diabetologia 1998, 41:54-58. 10.1007/s001250050866 9498630
-
(1998)
Diabetologia
, vol.41
, pp. 54-58
-
-
Poulton, J.1
Brown, M.S.2
Cooper, A.3
Marchington, D.R.4
Phillips, D.I.5
-
9
-
-
0033135836
-
Mitochondrial 16189 variant, thinness at birth, and type-2 diabetes. ALSPAC study team. Avon Longitudinal Study of Pregnancy and Childhood
-
10.1016/S0140-6736(98)05817-6 10232327
-
Casteels K Ong K Phillips D Bendall H Pembrey M Mitochondrial 16189 variant, thinness at birth, and type-2 diabetes. ALSPAC study team. Avon Longitudinal Study of Pregnancy and Childhood Lancet 1999, 353:1499-1500. 10.1016/S0140-6736(98)05817-6 10232327
-
(1999)
Lancet
, vol.353
, pp. 1499-1500
-
-
Casteels, K.1
Ong, K.2
Phillips, D.3
Bendall, H.4
Pembrey, M.5
-
10
-
-
33644876781
-
Epidemiology and Etiology of Cardiomyopathy in Africa
-
10.1161/CIRCULATIONAHA.105.542894 16330699
-
Sliwa K Damasceno A Mayosi BM Epidemiology and Etiology of Cardiomyopathy in Africa Circulation 2005, 112(23):3577-3583. 10.1161/ CIRCULATIONAHA.105.542894 16330699
-
(2005)
Circulation
, vol.112
, Issue.23
, pp. 3577-3583
-
-
Sliwa, K.1
Damasceno, A.2
Mayosi, B.M.3
-
11
-
-
0033919466
-
Genetic association studies in complex diseases
-
10.1038/sj.jhh.1001020 10878695
-
Keavney B Genetic association studies in complex diseases J Hum Hypertens 2000, 14:361-367. 10.1038/sj.jhh.1001020 10878695
-
(2000)
J Hum Hypertens
, vol.14
, pp. 361-367
-
-
Keavney, B.1
-
12
-
-
26444578213
-
Genotype at the -174G/C Polymorphism of the Interleukin-6 Gene Is Associated With Common Carotid Artery Intimal-Medial Thickness. Family Study and Meta-Analysis
-
10.1161/01.STR.0000182254.47941.96 16179573
-
Mayosi BM Avery PJ Baker M Gaukrodger N Imrie H Green FR Farrall M Watkins H Keavney B Genotype at the -174G/C Polymorphism of the Interleukin-6 Gene Is Associated With Common Carotid Artery Intimal-Medial Thickness. Family Study and Meta-Analysis Stroke 2005, 36:2215-2219. 10.1161/01.STR.0000182254.47941.96 16179573
-
(2005)
Stroke
, vol.36
, pp. 2215-2219
-
-
Mayosi, B.M.1
Avery, P.J.2
Baker, M.3
Gaukrodger, N.4
Imrie, H.5
Green, F.R.6
Farrall, M.7
Watkins, H.8
Keavney, B.9
-
13
-
-
0034606897
-
Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators
-
10841123
-
Keavney B McKenzie C Parish S Palmer A Clark S Youngman L Delepine M Lathrop M Peto R Collins R Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators Lancet 2000, 355:434-442. 10841123
-
(2000)
Lancet
, vol.355
, pp. 434-442
-
-
Keavney, B.1
McKenzie, C.2
Parish, S.3
Palmer, A.4
Clark, S.5
Youngman, L.6
Delepine, M.7
Lathrop, M.8
Peto, R.9
Collins, R.10
-
14
-
-
2142649184
-
Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome
-
10.1016/j.bbrc.2004.04.061 15120634
-
Ruppert V Nolte D Aschenbrenner T Pakuweit S Funck R Maisch B Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome Biochem Biophys Res Commun 2004, 318:535-543. 10.1016/j.bbrc.2004.04.061 15120634
-
(2004)
Biochem Biophys Res Commun
, vol.318
, pp. 535-543
-
-
Ruppert, V.1
Nolte, D.2
Aschenbrenner, T.3
Pakuweit, S.4
Funck, R.5
Maisch, B.6
-
15
-
-
34249997024
-
Replicating genotype-phenotype associations
-
NCI-NHGRI Working Group on Replication in Association Studies 10.1038/ 447655a 17554299
-
NCI-NHGRI Working Group on Replication in Association Studies Replicating genotype-phenotype associations Nature 2007, 447:655-660. 10.1038/447655a 17554299
-
(2007)
Nature
, vol.447
, pp. 655-660
-
-
|