Browsing by Author "Stowasser, Michael"
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- Item2022 World Hypertension League, Resolve To Save Lives and International Society of Hypertension dietary sodium (salt) global call to action(2023) Campbell, Norm R. C.; Whelton, Paul K.; Orias, Marcelo; Wainford, Richard D.; Cappuccio, Francesco P.; Ide, Nicole; Neal, Bruce; Cohn, Jennifer; Cobb, Laura K.; Webster, Jacqui; Trieu, Kathy; He, Feng J.; McLean, Rachael M.; Blanco-Metzler, Adriana; Woodward, Mark; Khan, Nadia; Kokubo, Yoshihiro; Nederveen, Leo; Arcand, JoAnne; MacGregor, Graham A.; Owolabi, Mayowa O.; Lisheng, Liu; Parati, Gianfranco; Lackland, Daniel T.; Charchar, Fadi J.; Williams, Bryan; Tomaszewski, Maciej; Romero, Cesar A.; Champagne, Beatriz; L'Abbe, Mary R.; Weber, Michael A.; Schlaich, Markus P.; Fogo, Agnes; Feigin, Valery L.; Akinyemi, Rufus; Inserra, Felipe; Menon, Bindu; Simas, Marcia; Neves, Mario Fritsch; Hristova, Krassimira; Pullen, Carolyn; Pandeya, Sanjay; Ge, Junbo; Jalil, Jorge E.; Wang, Ji-Guang; Wideimsky, Jiri; Kreutz, Reinhold; Wenzel, Ulrich; Stowasser, Michael; Arango, Manuel; Protogerou, Athanasios; Gkaliagkousi, Eugenia; Fuchs, Flavio Danni; Patil, Mansi; Chan, Andy Wai-Kwong; Nemcsik, Janos; Tsuyuki, Ross T.; Narasingan, Sanjeevi Nathamuni; Sarrafzadegan, Nizal; Ramos, Maria Eugenia; Yeo, Natalie; Rakugi, Hiromi; Ramirez, Agustin J.; Alvarez, Guillermo; Berbari, Adel; Kim, Cho-il; Ihm, Sang-Hyun; Chia, Yook-Chin; Unurjargal, Tsolmon; Park, Hye Kyung; Wahab, Kolawole; McGuire, Helen; Dashdorj, Naranjargal J.; Ishaq, Mohammed; Ona, Deborah Ignacia D.; Mercado-Asis, Leilani B.; Prejbisz, Aleksander; Leenaerts, Marianne; Simao, Carla; Pinto, Fernando; Almustafa, Bader Ali; Spaak, Jonas; Farsky, Stefan; Lovic, Dragan; Zhang, Xin-Hua
- ItemFamilial hyperaldosteronism: an European Reference Network on Rare Endocrine Conditions clinical practice guideline(2024) Mulatero, Paolo; Scholl, Ute, I; Fardella, Carlos E.; Charmandari, Evangelia; Januszewicz, Andrzej; Reincke, Martin; Gomez-Sanchez, Celso E.; Stowasser, Michael; Dekkers, Olaf M.We describe herein the European Reference Network on Rare Endocrine Conditions clinical practice guideline on diagnosis and management of familial forms of hyperaldosteronism. The guideline panel consisted of 10 experts in primary aldosteronism, endocrine hypertension, paediatric endocrinology, and cardiology as well as a methodologist. A systematic literature search was conducted, and because of the rarity of the condition, most recommendations were based on expert opinion and small patient series. The guideline includes a brief description of the genetics and molecular pathophysiology associated with each condition, the patients to be screened, and how to screen. Diagnostic and treatment approaches for patients with genetically determined diagnosis are presented. The recommendations apply to patients with genetically proven familial hyperaldosteronism and not to families with more than one case of primary aldosteronism without demonstration of a responsible pathogenic variant.