Prevalence of Liddle Syndrome Among Young Hypertension Patients of Undetermined Cause in a Chinese Population.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Works by Yang, Kun-Qi
Results: 15
1
2
RET c.1901G>A and Novel SLC12A3 Mutations in Familial Pheochromocytomas.
- Published in:
- Genes, 2022, v. 13, n. 5, p. 864, doi. 10.3390/genes13050864
- By:
- Publication type:
- Article
3
Apparent mineralocorticoid excess: comprehensive overview of molecular genetics.
- Published in:
- 2022
- By:
- Publication type:
- journal article
4
A novel frameshift mutation of epithelial sodium channel β-subunit leads to Liddle syndrome in an isolated case.
- Published in:
- Clinical Endocrinology, 2015, v. 82, n. 4, p. 611, doi. 10.1111/cen.12650
- By:
- Publication type:
- Article
5
Clinical characteristics of concurrent primary aldosteronism and renal artery stenosis: A retrospective case–control study.
- Published in:
- Clinical & Experimental Hypertension, 2021, v. 43, n. 1, p. 7, doi. 10.1080/10641963.2020.1790586
- By:
- Publication type:
- Article
6
Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome.
- Published in:
- Clinical & Experimental Hypertension, 2018, v. 40, n. 2, p. 107, doi. 10.1080/10641963.2017.1334799
- By:
- Publication type:
- Article
7
Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension.
- Published in:
- American Journal of Hypertension, 2020, v. 33, n. 7, p. 670, doi. 10.1093/ajh/hpaa037
- By:
- Publication type:
- Article
8
Hypertension and Brachydactyly Syndrome Associated With Vertebral Artery Malformation Caused by a PDE3A Missense Mutation.
- Published in:
- American Journal of Hypertension, 2020, v. 33, n. 2, p. 190, doi. 10.1093/ajh/hpz151
- By:
- Publication type:
- Article
9
Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia.
- Published in:
- American Journal of Hypertension, 2019, v. 32, n. 8, p. 752, doi. 10.1093/ajh/hpz053
- By:
- Publication type:
- Article
10
Lack of association between polymorphisms in interleukin (IL)-12, IL-12R, IL-23, IL-23R genes and Takayasu arteritis in a Chinese population.
- Published in:
- Inflammation Research, 2016, v. 65, n. 7, p. 543, doi. 10.1007/s00011-016-0938-x
- By:
- Publication type:
- Article
11
Gypenosides pre-treatment protects the brain against cerebral ischemia and increases neural stem cells/progenitors in the subventricular zone.
- Published in:
- International Journal of Developmental Neuroscience, 2014, v. 33, p. 49, doi. 10.1016/j.ijdevneu.2013.12.001
- By:
- Publication type:
- Article
12
Apparent mineralocorticoid excess caused by novel compound heterozygous mutations in HSD11B2 and characterized by early-onset hypertension and hypokalemia.
- Published in:
- Endocrine (1355008X), 2020, v. 70, n. 3, p. 607, doi. 10.1007/s12020-020-02460-9
- By:
- Publication type:
- Article
13
Childhood-Onset Refractory Hypertension Results from Neurofibromatosis Type 1 Caused by a Splicing NF1 Mutation.
- Published in:
- Kidney & Blood Pressure Research, 2023, v. 48, n. 1, p. 568, doi. 10.1159/000533144
- By:
- Publication type:
- Article
14
Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation.
- Published in:
- Kidney & Blood Pressure Research, 2020, v. 45, n. 4, p. 603, doi. 10.1159/000507580
- By:
- Publication type:
- Article
15
Truncated Epithelial Sodium Channel β Subunit Responsible for Liddle Syndrome in a Chinese Family.
- Published in:
- Kidney & Blood Pressure Research, 2019, v. 44, n. 5, p. 942, doi. 10.1159/000500919
- By:
- Publication type:
- Article