Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Hypertension and NF1[original query] |
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Identification of polymorphisms in the human 11beta-hydroxysteroid dehydrogenase type 2 gene promoter: functional characterization and relevance for salt sensitivity. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2007 Nov 21 (13): 3618-28. Alikhani-Koupaei Rasoul, Fouladkou Fatemeh, Fustier Pierre, Cenni Bruno, Sharma Arya M, Deter Hans-Christian, Frey Brigitte M, Frey Felix |
Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing. Annals of surgical oncology 2013 May 20 (5): 1444-50. Fishbein Lauren, Merrill Shana, Fraker Douglas L, Cohen Debbie L, Nathanson Katherine |
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ?43% of 35 Families With Midaortic Syndrome. Hypertension (Dallas, Tex. : 1979) 2018 2 71 (4): 691-699. Warejko Jillian K, Schueler Markus, Vivante Asaf, Tan Weizhen, Daga Ankana, Lawson Jennifer A, Braun Daniela A, Shril Shirlee, Amann Kassaundra, Somers Michael J G, Rodig Nancy M, Baum Michelle A, Daouk Ghaleb, Traum Avram Z, Kim Heung Bae, Vakili Khashayar, Porras Diego, Lock James, Rivkin Michael J, Chaudry Gulraiz, Smoot Leslie B, Singh Michael N, Smith Edward R, Mane Shrikant M, Lifton Richard P, Stein Deborah R, Ferguson Michael A, Hildebrandt Friedhe |
Genetics of renovascular hypertension in children. Journal of hypertension 2020 Oct 38 (10): 1964-1970. Viering Daan H H M, Chan Melanie M Y, Hoogenboom Lieke, Iancu Daniela, de Baaij Jeroen H F, Tullus Kjell, Kleta Robert, Bockenhauer Detl |
Systemic hypertension followed by insidious stroke in a 12-year-old boy with childhood neurofibromatosis type 1 presenting with renal and cerebral artery vasculopathy. The Turkish journal of pediatrics 2020 1 61 (4): 629-634. Lee Meng-Luen, Chang Tung-Ming, Yang Rei-Cheng, Yang Albert D, Chen Mi |
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