Pesquisa | Portal de Pesquisa da BVS Enfermagem

Cacciottolo, T M; Perikari, A; van der Klaauw, A; Henning, E; Stadler, L K J; Keogh, J; Farooqi, I S; Tenin, G; Keavney, B; Ryan, E; Budd, R; Bewley, M; Coelho, P; Rumsey, W; Sanchez, Y; McCafferty, J; Dockrell, D; Walmsley, S; Whyte, M; Liu, Y; Choy, M-K; Tenin, G; Abraham, S; Black, G; Keavney, B; Ford, T; Stanley, B; Good, R; Rocchiccioli, P; McEntegart, M; Watkins, S; Eteiba, H; Shaukat, A; Lindsay, M; Robertson, K; Hood, S; McGeoch, R; McDade, R; Sidik, N; McCartney, P; Corcoran, D; Collison, D; Rush, C; McConnachie, A; Touyz, R; Oldroyd, K; Berry, Colin; Gazdagh, G; Diver, L; Marshall, J.

QJM ; 112(9): 724-729, 2019 Sep 01.

Artigo em Inglês | MEDLINE | ID: mdl-31505685

17.

Genetic factors in human obesity.

Farooqi, I S; O'Rahilly, S.

Obes Rev ; 8 Suppl 1: 37-40, 2007 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-17316299

18.

Leptin substitution results in the induction of menstrual cycles in an adolescent with leptin deficiency and hypogonadotropic hypogonadism.

von Schnurbein, J; Moss, A; Nagel, S A; Muehleder, H; Debatin, K M; Farooqi, I S; Wabitsch, M.

Horm Res Paediatr ; 77(2): 127-33, 2012.

Artigo em Inglês | MEDLINE | ID: mdl-22343341

19.

Prolonged successful therapy for hyperinsulinaemic hypoglycaemia after gastric bypass: the pathophysiological role of GLP1 and its response to a somatostatin analogue.

Myint, K S; Greenfield, J R; Farooqi, I S; Henning, E; Holst, J J; Finer, N.

Eur J Endocrinol ; 166(5): 951-5, 2012 May.

Artigo em Inglês | MEDLINE | ID: mdl-22408121

20.

Triple H syndrome: a novel autoimmune endocrinopathy characterized by dysfunction of the hippocampus, hair follicle, and hypothalamic-pituitary adrenal axis.

Farooqi, I S; Jones, M K; Evans, M; O'Rahilly, S; Hodges, J R.

J Clin Endocrinol Metab ; 85(8): 2644-8, 2000 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-10946860

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Increased body mass index is associated with specific regional alterations in brain structure.

Food images engage subliminal motivation to seek food.

Homozygosity for a novel missense mutation in the leptin receptor gene (P316T) in two Egyptian cousins with severe early onset obesity.

Human obesity as a heritable disorder of the central control of energy balance.

A frameshift mutation in MC4R associated with dominantly inherited human obesity.

Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency.

Monogenic human obesity syndromes.

A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism.

Two novel missense mutations in g protein-coupled receptor 54 in a patient with hypogonadotropic hypogonadism.

The CART gene and human obesity: mutational analysis and population genetics.

TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiency.

The role of melanocortin signalling in the control of body weight: evidence from human and murine genetic models.

A comparative study of risk factors for acute myocardial infarction amongst men of Indo-origin in Trinidad and the UK.

Abnormal haemorheology, endothelial function and thrombogenesis in relation to hypertension in acute (ictus < 12 h) stroke patients: the West Birmingham Stroke Project.

Sequential alterations in haemorheology, endothelial dysfunction, platelet activation and thrombogenesis in relation to prognosis following acute stroke: The West Birmingham Stroke Project.

Scientific Business Abstracts of the 113th Annual Meeting of the Association of Physicians of Great Britain and Ireland.

Genetic factors in human obesity.

Leptin substitution results in the induction of menstrual cycles in an adolescent with leptin deficiency and hypogonadotropic hypogonadism.

Prolonged successful therapy for hyperinsulinaemic hypoglycaemia after gastric bypass: the pathophysiological role of GLP1 and its response to a somatostatin analogue.

Triple H syndrome: a novel autoimmune endocrinopathy characterized by dysfunction of the hippocampus, hair follicle, and hypothalamic-pituitary adrenal axis.