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Results: 1-9 |
Results: 9
The use of botulinum toxin-A in the treatment of patients with fibromyalgia
Authors: Asherson, RA Pascoe, L
Citation: Ra. Asherson et L. Pascoe, The use of botulinum toxin-A in the treatment of patients with fibromyalgia, J RHEUMATOL, 28(7), 2001, pp. 1740-1740
Angiotensin-converting enzyme and angiotensinogen gene polymorphisms are non-randomly distributed in oral contraceptive-induced hypertension.
Authors: Mulatero, P Rabbia, F di Cella, SM Schiavone, D Plazzotta, C Pascoe, L Veglio, F
Citation: P. Mulatero et al., Angiotensin-converting enzyme and angiotensinogen gene polymorphisms are non-randomly distributed in oral contraceptive-induced hypertension., J HYPERTENS, 19(4), 2001, pp. 713-719
Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11 beta-hydroxylase) and CYP11B2 (aldosterone synthase) cause steroid 11 beta-hydroxylase deficiency and congenital adrenal hyperplasia
Authors: Portrat, S Mulatero, P Curnow, KM Chaussain, JL Morel, Y Pascoe, L
Citation: S. Portrat et al., Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11 beta-hydroxylase) and CYP11B2 (aldosterone synthase) cause steroid 11 beta-hydroxylase deficiency and congenital adrenal hyperplasia, J CLIN END, 86(7), 2001, pp. 3197-3201
Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domain
Authors: Nikkila, H McMillan, DR Nunez, BS Pascoe, L Curnow, KM White, PC
Citation: H. Nikkila et al., Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domain, MOL ENDOCR, 14(9), 2000, pp. 1351-1364
CYP11B2 gene polymorphisms in idiopathic hyperaldosteronism
Authors: Mulatero, P Schiavone, D Fallo, F Rabbia, F Pilon, C Chiandussi, L Pascoe, L Veglio, F
Citation: P. Mulatero et al., CYP11B2 gene polymorphisms in idiopathic hyperaldosteronism, HYPERTENSIO, 35(3), 2000, pp. 694-698
The efficiency of genetic analysis of DNA from aged siblings to detect chromosomal regions implicated in longevity
Authors: Nemani, M Sahbatou, M Blanche, H Thomas, G Pascoe, L
Citation: M. Nemani et al., The efficiency of genetic analysis of DNA from aged siblings to detect chromosomal regions implicated in longevity, MECH AGE D, 119(1-2), 2000, pp. 25-39
Genetic, biochemical, and clinical studies of patients with A328V or R213Cmutations in 11 beta HSD2 causing apparent mineralocorticoid excess
Authors: Morineau, G Marc, JM Boudi, A Galons, H Gourmelen, M Corvol, P Pascoe, L Fiet, J
Citation: G. Morineau et al., Genetic, biochemical, and clinical studies of patients with A328V or R213Cmutations in 11 beta HSD2 causing apparent mineralocorticoid excess, HYPERTENSIO, 34(3), 1999, pp. 435-441
Prenatal diagnosis and treatment of 11 beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia
Authors: Cerame, BI Newfield, RS Pascoe, L Curnow, KM Nimkarn, S Roe, TF New, MI Wilson, RC
Citation: Bi. Cerame et al., Prenatal diagnosis and treatment of 11 beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia, J CLIN END, 84(9), 1999, pp. 3129-3134
Structural analysis and evaluation of the 11 beta-hydroxysteroid dehydrogenase type 2 (11 beta-HSD2) gene in human essential hypertension
Authors: Brand, E Kato, N Chatelain, N Krozowski, ZS Jeunemaitre, X Corvol, P Plouin, PF Cambien, F Pascoe, L Soubrier, F
Citation: E. Brand et al., Structural analysis and evaluation of the 11 beta-hydroxysteroid dehydrogenase type 2 (11 beta-HSD2) gene in human essential hypertension, J HYPERTENS, 16(11), 1998, pp. 1627-1633
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