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Hypertension
Citations 1-10 of 51 total displayed.
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Most recent content
(1 Jun 2009):
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Letters to JMG
Do mutations of the Pendred syndrome gene, SLC26A4, confer resistance to asthma and hypertension?
- A C Madeo, A Manichaikul, S P Pryor, A J Griffith
J. Med. Genet. 2009 46: 405 -406; published online before print as 10.1136/jmg.2008.063610
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Past content
(since Jul 2000):
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Original articles
A new nonsense mutation of SMAD8 associated with pulmonary arterial hypertension
- M Shintani, H Yagi, T Nakayama, T Saji, R Matsuoka
J. Med. Genet. 2009 46: 331 -337; published online before print as 10.1136/jmg.2008.062703
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Original articles
Genetic analysis of 56 polymorphisms in 17 genes involved in methionine metabolism in patients with abdominal aortic aneurysm
- B Giusti, C Saracini, P Bolli, A Magi, I Sestini, E Sticchi, G Pratesi, R Pulli, C Pratesi, R Abbate
J. Med. Genet. 2008 45: 721 -730; published online before print as 10.1136/jmg.2008.057851
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Original articles
Prevalence and heritability of the metabolic syndrome and its individual components in a Dutch isolate: the Erasmus Rucphen Family study
- P Henneman, Y S Aulchenko, R R Frants, K W van Dijk, B A Oostra, C M van Duijn
J. Med. Genet. 2008 45: 572 -577; published online before print as 10.1136/jmg.2008.058388
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Original articles
Genetic risk for myocardial infarction determined by polymorphisms of candidate genes in a Japanese population
- Y Yamada, K Kato, M Oguri, T Fujimaki, K Yokoi, H Matsuo, S Watanabe, N Metoki, H Yoshida, K Satoh, S Ichihara, Y Aoyagi, A Yasunaga, H Park, M Tanaka, Y Nozawa
J. Med. Genet. 2008 45: 216 -221; published online before print as 10.1136/jmg.2007.054387
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Review
Dissection of the aorta in Turner syndrome: two cases and review of 85 cases in the literature
- M Carlson, M Silberbach
J. Med. Genet. 2007 44: 745 -749; published online before print as 10.1136/jmg.2007.052019
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Original articles
A genome-wide scan for genes involved in primary vesicoureteric reflux
- H Kelly, C M Molony, J M Darlow, M E Pirker, A Yoneda, A J Green, P Puri, D E Barton
J. Med. Genet. 2007 44: 710 -717; published online before print as 10.1136/jmg.2007.051086
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Short reports
Genetic screening for pheochromocytoma: should SDHC gene analysis be included?
- M Mannelli, T Ercolino, V Giachè, L Simi, C Cirami, G Parenti
J. Med. Genet. 2007 44: 586 -587; published online before print as 10.1136/jmg.2007.051045
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Letters to JMG
Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension
- Ana Carolina Braga Marçano, Beverley Burke, Johannie Gungadoo, Chris Wallace, Pamela J Kaisaki, Peng Y Woon, Martin Farrall, David Clayton, Morris Brown, Anna Dominiczak, John M Connell, John Webster, Mark Lathrop, Mark Caulfield, Nilesh Samani, Dominique Gauguier, Patricia B Munroe
J. Med. Genet. 2007 44: 603 -605; published online before print as 10.1136/jmg.2007.049718
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Original articles
Schimke immuno-osseous dysplasia: a clinicopathological correlation
- J Marietta Clewing, Barbara C Antalfy, Thomas Lücke, Behzad Najafian, Katja M Marwedel, Akira Hori, Ralph M Powel, A F Safo Do, Lydia Najera, Karen SantaCruz, M John Hicks, Dawna L Armstrong, Corndins F Boerkoel
J. Med. Genet. 2007 44: 122 -130; published online before print as 10.1136/jmg.2006.044313
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