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Page 1
Did you mean ute school (741 results)?
Diagnosis and treatment of primary aldosteronism.
Reincke M, Bancos I, Mulatero P, Scholl UI, Stowasser M, Williams TA. Reincke M, et al. Among authors: scholl ui. Lancet Diabetes Endocrinol. 2021 Dec;9(12):876-892. doi: 10.1016/S2213-8587(21)00210-2. Lancet Diabetes Endocrinol. 2021. PMID: 34798068 Free article. Review.
[Secondary hypertension].
van der Giet M, Scholl U. van der Giet M, et al. Among authors: scholl u. MMW Fortschr Med. 2022 Apr;164(Suppl 1):35-41. doi: 10.1007/s15006-022-0722-5. MMW Fortschr Med. 2022. PMID: 35359291 German. No abstract available.
Genetics of Primary Aldosteronism.
Scholl UI. Scholl UI. Hypertension. 2022 May;79(5):887-897. doi: 10.1161/HYPERTENSIONAHA.121.16498. Epub 2022 Feb 10. Hypertension. 2022. PMID: 35139664 Free PMC article. Review.
The genetics of hypertension.
Stölting G, Tran Vo KN, Haus J, Scholl UI. Stölting G, et al. Among authors: scholl ui. Nat Rev Nephrol. 2026 Feb;22(2):137-151. doi: 10.1038/s41581-025-01020-6. Epub 2025 Nov 11. Nat Rev Nephrol. 2026. PMID: 41219524 Review.
Somatic Mutations in MCOLN3 Are Associated With Aldosterone-Producing Adenomas.
van Rooyen D, Bandulik S, Coon GA, Laukemper M, Kumar-Sinha C, Udager AM, Lerario AM, Lee C, Wachtel H, Cohen DL, Luther JM, Giordano TJ, Scholl UI, Butz F, Popp B, Turcu AF, Warth R, Rainey WE, Rege J. van Rooyen D, et al. Among authors: scholl ui. Hypertension. 2025 Oct;82(10):1778-1788. doi: 10.1161/HYPERTENSIONAHA.125.24909. Epub 2025 Aug 7. Hypertension. 2025. PMID: 40772318 Free PMC article.
CaV3.2 (CACNA1H) in Primary Aldosteronism.
Dinh HA, Stölting G, Scholl UI. Dinh HA, et al. Among authors: scholl ui. Handb Exp Pharmacol. 2023;279:249-262. doi: 10.1007/164_2023_660. Handb Exp Pharmacol. 2023. PMID: 37311830 Review.
Genetic causes of primary aldosteronism.
Seidel E, Schewe J, Scholl UI. Seidel E, et al. Among authors: scholl ui. Exp Mol Med. 2019 Nov 6;51(11):1-12. doi: 10.1038/s12276-019-0337-9. Exp Mol Med. 2019. PMID: 31695023 Free PMC article. Review.
A Novel De Novo Gain-of-Function CACNA1D Variant in Neurodevelopmental Disease With Congenital Tremor, Seizures, and Hypotonia.
Dannenberg F, Von Moers A, Bittigau P, Lange J, Wiegand S, Török F, Stölting G, Striessnig J, Motazacker MM, Broekema MF, Schuelke M, Kaindl AM, Scholl UI, Ortner NJ. Dannenberg F, et al. Among authors: scholl ui. Neurol Genet. 2024 Sep 6;10(5):e200186. doi: 10.1212/NXG.0000000000200186. eCollection 2024 Oct. Neurol Genet. 2024. PMID: 39246741 Free PMC article.
60 results