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Results: 1-10 |
Results: 10
Abnormal haemorheology, endothelial function and thrombogenesis in relation to hypertension in acute (ictus < 12 h) stroke patients: the West Birmingham Stroke Project
Authors: Lip, GYH Blann, AD Farooqi, IS Zarifis, J Sagar, G Beevers, DG
Citation: Gyh. Lip et al., Abnormal haemorheology, endothelial function and thrombogenesis in relation to hypertension in acute (ictus < 12 h) stroke patients: the West Birmingham Stroke Project, BL COAG FIB, 12(4), 2001, pp. 307-315
Uncoupling protein 3 genetic variants in human obesity: the c-55t promoterpolymorphism is negatively correlated with body mass index in a UK Caucasian population
Authors: Halsall, DJ Luan, J Saker, P Huxtable, S Farooqi, IS Keogh, J Wareham, NJ O'Rahilly, S
Citation: Dj. Halsall et al., Uncoupling protein 3 genetic variants in human obesity: the c-55t promoterpolymorphism is negatively correlated with body mass index in a UK Caucasian population, INT J OBES, 25(4), 2001, pp. 472-477
Metabolism - Partial leptin deficiency and human adiposity
Authors: Farooqi, IS Keogh, JM Kamath, S Jones, S Gibson, WT Trussell, R Jebb, SA Lip, GYH O'Rahilly, S
Citation: Is. Farooqi et al., Metabolism - Partial leptin deficiency and human adiposity, NATURE, 414(6859), 2001, pp. 34-35
The role of melanocortin signalling in the control of body weight: evidence from human and murine genetic models
Authors: Yeo, GSH Farooqi, IS Challis, BG Jackson, RS O'Rahilly, S
Citation: Gsh. Yeo et al., The role of melanocortin signalling in the control of body weight: evidence from human and murine genetic models, QJM-MON J A, 93(1), 2000, pp. 7-14
Genetics of body-weight regulation
Authors: Barsh, GS Farooqi, IS O'Rahilly, S
Citation: Gs. Barsh et al., Genetics of body-weight regulation, NATURE, 404(6778), 2000, pp. 644-651
Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency
Authors: Farooqi, IS Yeo, GSH Keogh, JM Aminian, S Jebb, SA Butler, G Cheetham, T O'Rahilly, S
Citation: Is. Farooqi et al., Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency, J CLIN INV, 106(2), 2000, pp. 271-279
Triple H syndrome: A novel autoimmune endocrinopathy characterized by dysfunction of the hippocampus, hair follicle, and hypothalamic-pituitary-adrenal axis
Authors: Farooqi, IS Jones, MK Evans, M O'Rahilly, S Hodges, JR
Citation: Is. Farooqi et al., Triple H syndrome: A novel autoimmune endocrinopathy characterized by dysfunction of the hippocampus, hair follicle, and hypothalamic-pituitary-adrenal axis, J CLIN END, 85(8), 2000, pp. 2644-2648
The CART gene and human obesity - Mutational analysis and population genetics
Authors: Challis, BG Yeo, GSH Farooqi, IS Luan, J Aminian, S Halsall, DJ Keogh, JM Wareham, NJ O'Rahilly, S
Citation: Bg. Challis et al., The CART gene and human obesity - Mutational analysis and population genetics, DIABETES, 49(5), 2000, pp. 872-875
Recent advances in the genetics of severe childhood obesity
Authors: Farooqi, IS O'Rahilly, S
Citation: Is. Farooqi et S. O'Rahilly, Recent advances in the genetics of severe childhood obesity, ARCH DIS CH, 83(1), 2000, pp. 31-34
Effects of recombinant leptin therapy in a child with congenital leptin deficiency
Authors: Farooqi, IS Jebb, SA Langmack, G Lawrence, E Cheetham, CH Prentice, AM Hughes, IA McCamish, MA O'Rahilly, S
Citation: Is. Farooqi et al., Effects of recombinant leptin therapy in a child with congenital leptin deficiency, N ENG J MED, 341(12), 1999, pp. 879-884
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