Chih-Chien Sung
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Explore the profile of Chih-Chien Sung including associated specialties, affiliations and a list of published articles.
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45
Citations
457
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Recent Articles
1.
Chou Y, Chen H, Hsu B, Yang C, Chen C, Lee Y, et al.
Kidney Int
. 2024 Jul;
106(4):658-670.
PMID: 39084257
IgA nephropathy (IgAN) is the most common type of glomerulonephritis that frequently progresses to kidney failure. However, the molecular pathogenesis underlying IgAN remains largely unknown. Here, we investigated the role...
2.
Liu C, Chen C, Sung C
Nephrology (Carlton)
. 2024 Apr;
29(7):442-445.
PMID: 38599621
Icodextrin has been widely prescribed for peritoneal dialysis (PD) patients with inadequate ultrafiltration, but icodextrin induced acute generalized exanthematous pustulosis (AGEP) has been not well recognized in clinical practice. We...
3.
Lin C, Ding Y, Huang S, Chen Y, Lee H, Sung C, et al.
Front Endocrinol (Lausanne)
. 2024 Mar;
15:1291160.
PMID: 38487341
Context: Although a monoallelic mutation in the calcium-sensing receptor () gene causes familial hypocalciuric hypercalcemia (FHH), the functional characterization of the identified mutation linked to the clinical response to calcimimetics...
4.
Chen C, Yang S, Hsu Y, Sung C, Chu P, Wu C, et al.
Front Med (Lausanne)
. 2023 Jun;
10:1189243.
PMID: 37283622
Background: Rare cases of or relapsed kidney diseases associated with vaccination against coronavirus disease 2019 (COVID-19) have been increasingly reported. The aim of this study was to report the incidence,...
5.
Mak A, Sung C, Pisitkun T, Khositseth S, Knepper M
J Physiol
. 2023 Apr;
602(13):3191-3206.
PMID: 37114282
Animal models of a variety of acquired nephrogenic diabetes insipidus (NDI) disorders have identified a common feature: all such models are associated with the loss of aquaporin-2 (AQP2) from collecting...
6.
Wan E, Iancu D, Ashton E, Siew K, Mohidin B, Sung C, et al.
Kidney Int Rep
. 2023 Mar;
8(3):556-565.
PMID: 36938092
Introduction: Clinically distinguishing patients with the inherited salt-losing tubulopathies (SLTs), Gitelman or Bartter syndrome (GS or BS) from other causes of hypokalemia (LK) patients is difficult, and genotyping is costly....
7.
Sung C, Poll B, Lin S, Murillo-de-Ozores A, Chou C, Chen L, et al.
J Am Soc Nephrol
. 2022 Aug;
33(11):2040-2058.
PMID: 35918145
Background: Ureteral obstruction is marked by disappearance of the vasopressin-dependent water channel aquaporin-2 (AQP2) in the renal collecting duct and polyuria upon reversal. Most studies of unilateral ureteral obstruction (UUO)...
8.
Tseng M, Yang S, Sung C, Ding J, Hsu Y, Chu S, et al.
Front Genet
. 2022 Jul;
13:875013.
PMID: 35846113
is primarily expressed in the brain and distal convoluted tubule (DCT) of the kidney. Mutations in have been reported to cause hypomagnesemia, seizure, and intellectual disability (HSMR) syndrome. However, the...
9.
Lin C, Sung C, Yang S, Chen Y, Huang S, Lin S
FASEB J
. 2022 May;
36(6):e22363.
PMID: 35621709
Mutations in the Kelch-like 3 (KLHL3) gene are the most common cause of inherited pseudohypoaldosteronism type II (PHAII) featuring thiazide-sensitive hypertension and hyperkalemic metabolic acidosis. Although Klhl3 knock-in (KI) mice...
10.
Chen H, Sung C
BMC Nephrol
. 2022 Feb;
23(1):81.
PMID: 35216554
Background: Empty sella syndrome is characterized by a constellation of symptoms that encompass various systems, and includes endocrine, neurologic, ophthalmologic, and psychiatric presentations. We here report a case of a...