Scholl UI - Search Results

1

Familial hyperaldosteronism: an European Reference Network on Rare Endocrine Conditions clinical practice guideline.

Mulatero P, Scholl UI, Fardella CE, Charmandari E, Januszewicz A, Reincke M, Gomez-Sanchez CE, Stowasser M, Dekkers OM. Mulatero P, et al. Among authors: scholl ui. Eur J Endocrinol. 2024 Mar 30;190(4):G1-G14. doi: 10.1093/ejendo/lvae041. Eur J Endocrinol. 2024. PMID: 38571460

2

Adrenal Anion Channels: New Roles in Zona Glomerulosa Physiology and in the Pathophysiology of Primary Aldosteronism.

Stölting G, Scholl UI. Stölting G, et al. Among authors: scholl ui. Handb Exp Pharmacol. 2024;283:59-79. doi: 10.1007/164_2023_680. Handb Exp Pharmacol. 2024. PMID: 37495852

3

Ca_V3.2 (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.

4

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.

5

T- and L-Type Calcium Channels Maintain Calcium Oscillations in the Murine Zona Glomerulosa.

Dinh HA, Volkert M, Secener AK, Scholl UI, Stölting G. Dinh HA, et al. Among authors: scholl ui. Hypertension. 2024 Apr;81(4):811-822. doi: 10.1161/HYPERTENSIONAHA.123.21798. Epub 2024 Feb 16. Hypertension. 2024. PMID: 38507511 Free PMC article.

6

Isradipine therapy in Cacna1dIle772Met/+ mice ameliorates primary aldosteronism and neurologic abnormalities.

Stölting G, Dinh HA, Volkert M, Hellmig N, Schewe J, Hennicke L, Seidel E, Oberacher H, Zhang J, Lifton RP, Urban I, Long M, Rivalan M, Nottoli T, Scholl UI. Stölting G, et al. Among authors: scholl ui. JCI Insight. 2023 Oct 23;8(20):e162468. doi: 10.1172/jci.insight.162468. JCI Insight. 2023. PMID: 37698934 Free PMC article.

7

Generation of sheep with defined FecB^B and TBXT mutations and porcine blastocysts with KCNJ5^G151R/+ mutation using prime editing.

Zhou S, Lenk LJ, Gao Y, Wang Y, Zhao X, Pan M, Huang S, Sun K, Kalds P, Luo Q, Lillico S, Sonstegard T, Scholl UI, Ma B, Petersen B, Chen Y, Wang X. Zhou S, et al. Among authors: scholl ui. BMC Genomics. 2023 Jun 12;24(1):313. doi: 10.1186/s12864-023-09409-y. BMC Genomics. 2023. PMID: 37308830 Free PMC article.

8

Integration of artificial intelligence and plasma steroidomics with laboratory information management systems: application to primary aldosteronism.

Constantinescu G, Schulze M, Peitzsch M, Hofmockel T, Scholl UI, Williams TA, Lenders JWM, Eisenhofer G. Constantinescu G, et al. Among authors: scholl ui. Clin Chem Lab Med. 2022 Jul 18;60(12):1929-1937. doi: 10.1515/cclm-2022-0470. Print 2022 Nov 25. Clin Chem Lab Med. 2022. PMID: 35851438 Free article.

9

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.

10

A Novel Homozygous KLHL3 Mutation as a Cause of Autosomal Recessive Pseudohypoaldosteronism Type II Diagnosed Late in Life.

Etges A, Hellmig N, Walenda G, Haddad BG, Machtens JP, Morosan T, Rump LC, Scholl UI. Etges A, et al. Among authors: scholl ui. Nephron. 2022;146(4):418-428. doi: 10.1159/000521626. Epub 2022 Jan 28. Nephron. 2022. PMID: 35093948 Free PMC article.

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