Hypertension

Gender specific association of aldosterone synthase gene polymorphism with renal survival in patients with IgA nephropathy
J Song, I Narita, S Goto, N Saito, K Omori, F Sato, J Ajiro, D Saga, D Kondo, M Sakatsume, F Gejyo

Journal of Medical Genetics May 2003, 40 (5) 372-376; DOI: 10.1136/jmg.40.5.372
Evidence for linkage and association of the markers near the LPL gene with hypertension in Chinese families
W J Yang, J F Huang, C L Yao, Z J Fan, D L Ge, W Q Gan, G Y Huang, R T Hui, Y Shen, B Q Qiang, D F Gu

Journal of Medical Genetics May 2003, 40 (5) e57; DOI: 10.1136/jmg.40.5.e57
Haptoglobin and its association with the HELLP syndrome
M T M Raijmakers, E M Roes, R H M te Morsche, E A P Steegers, W H M Peters

Journal of Medical Genetics Mar 2003, 40 (3) 214-216; DOI: 10.1136/jmg.40.3.214
Relationship between microsatellite polymorphism in the haem oxygenase-1 gene promoter and longevity of the normal Japanese population
M Yamaya, K Nakayama, S Ebihara, H Hirai, S Higuchi, H Sasaki

Journal of Medical Genetics Feb 2003, 40 (2) 146-148; DOI: 10.1136/jmg.40.2.146
Quality of life in a family based genetic cascade screening programme for familial hypercholesterolaemia: a longitudinal study among participants
M C van Maarle, M E A Stouthard, G J Bonsel

Journal of Medical Genetics Jan 2003, 40 (1) e3; DOI: 10.1136/jmg.40.1.e3
Heterozygous P250L mutation of fibroblast growth factor receptor 3 in a case of isolated craniosynostosis
S Schindler, M Friedrich, H Wagener, B Lorenz, M N Preising

Journal of Medical Genetics Oct 2002, 39 (10) 764-766; DOI: 10.1136/jmg.39.10.764
Cardiovascular manifestations in 75 patients with Williams syndrome
M Eronen, M Peippo, A Hiippala, M Raatikka, M Arvio, R Johansson, M Kähkönen

Journal of Medical Genetics Aug 2002, 39 (8) 554-558; DOI: 10.1136/jmg.39.8.554
Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia
C Olivieri, E Mira, G Delù, F Pagella, A Zambelli, L Malvezzi, E Buscarini, C Danesino

Journal of Medical Genetics Jul 2002, 39 (7) e39; DOI: 10.1136/jmg.39.7.e39
An investigation of ACE as a risk factor for dementia and cognitive decline in the general population
A G Yip, C Brayne, D Easton, D C Rubinsztein

Journal of Medical Genetics Jun 2002, 39 (6) 403-406; DOI: 10.1136/jmg.39.6.403
Identification of cryptic splice site, exon skipping, and novel point mutations in type I CD36 deficiency
H Hanawa, K Watanabe, T Nakamura, Y Ogawa, K Toba, I Fuse, M Kodama, K Kato, K Fuse, Y Aizawa

Journal of Medical Genetics Apr 2002, 39 (4) 286-291; DOI: 10.1136/jmg.39.4.286

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