Search Results - "Sung, Chih‐Chien"

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  1. 1

    ‘Aquaporin‐omics’: mechanisms of aquaporin‐2 loss in polyuric disorders by Mak, Angela, Sung, ChihChien, Pisitkun, Trairak, Khositseth, Sookkasem, Knepper, Mark A.

    Published in The Journal of physiology (01-07-2024)
    “…Animal models of a variety of acquired nephrogenic diabetes insipidus (NDI) disorders have identified a common feature: all such models are associated with the…”
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  2. 2

    Icodextrin‐induced acute generalized exanthematous pustulosis in a patient with peritoneal dialysis by Liu, Chun‐Hao, Chen, Chien‐Chou, Sung, ChihChien

    Published in Nephrology (Carlton, Vic.) (01-07-2024)
    “…Icodextrin has been widely prescribed for peritoneal dialysis (PD) patients with inadequate ultrafiltration, but icodextrin induced acute generalized…”
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  3. 3

    Role of Vitamin D in Insulin Resistance by Sung, Chih-Chien, Liao, Min-Tser, Lu, Kuo-Cheng, Wu, Chia-Chao

    Published in Journal of biomedicine & biotechnology (01-01-2012)
    “…Vitamin D is characterized as a regulator of homeostasis of bone and mineral metabolism, but it can also provide nonskeletal actions because vitamin D…”
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  4. 4

    Independent Determinants of Appetite Impairment among Patients with Stage 3 or Higher Chronic Kidney Disease: A Prospective Study by Sung, Chih-Chien, Liao, Min-Tser, Chao, Chia-Ter

    Published in Nutrients (01-08-2021)
    “…Protein-energy wasting (PEW) is an important complication resulting from chronic kidney disease (CKD). Appetite impairment contributes significantly to PEW in…”
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  5. 5

    A young man with secondary adrenal insufficiency due to empty sella syndrome by Chen, Hsi-Chih, Sung, Chih-Chien

    Published in BMC nephrology (25-02-2022)
    “…Empty sella syndrome is characterized by a constellation of symptoms that encompass various systems, and includes endocrine, neurologic, ophthalmologic, and…”
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  6. 6

    Phytobezoar-induced small bowel obstruction in an elderly patient undergoing dialysis: a case report by Wei, Kuang-Yu, Sung, Chih-Chien, Lin, Shih-Hua

    Published in Journal of international medical research (01-10-2020)
    “…A phytobezoar is defined as an accumulation of poorly digested fruit and vegetable fibers in the gastrointestinal tract. Phytobezoar-induced small bowel…”
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  7. 7

    Novel CNNM2 Mutation Responsible for Autosomal-Dominant Hypomagnesemia With Seizure by Tseng, Min-Hua, Yang, Sung-Sen, Sung, Chih-Chien, Ding, Jhao-Jhuang, Hsu, Yu-Juei, Chu, Shih-Ming, Lin, Shih-Hua

    Published in Frontiers in genetics (29-06-2022)
    “…CNNM2 is primarily expressed in the brain and distal convoluted tubule (DCT) of the kidney. Mutations in CNNM2 have been reported to cause hypomagnesemia,…”
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  8. 8

    Identification and characterization of a novel CASR mutation causing familial hypocalciuric hypercalcemia by Lin, Chien-Ming, Ding, Yi-Xuan, Huang, Shih-Ming, Chen, Ying-Chuan, Lee, Hwei-Jen, Sung, Chih-Chien, Lin, Shih-Hua

    Published in Frontiers in endocrinology (Lausanne) (29-02-2024)
    “…Although a monoallelic mutation in the calcium-sensing receptor ( ) gene causes familial hypocalciuric hypercalcemia (FHH), the functional characterization of…”
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  9. 9

    Insulin Resistance in Patients with Chronic Kidney Disease by Liao, Min-Tser, Sung, Chih-Chien, Hung, Kuo-Chin, Wu, Chia-Chao, Lo, Lan, Lu, Kuo-Cheng

    Published in Journal of biomedicine & biotechnology (01-01-2012)
    “…Metabolic syndrome and its components are associated with chronic kidney disease (CKD) development. Insulin resistance (IR) plays a central role in the…”
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  10. 10

    Association of Serum Phosphate with Low Handgrip Strength in Patients with Advanced Chronic Kidney Disease by Tsai, Ping-Huang, Yang, Hsiu-Chien, Lin, Chin, Sung, Chih-Chien, Chu, Pauling, Hsu, Yu-Juei

    Published in Nutrients (14-10-2021)
    “…Muscle wasting and hyperphosphatemia are becoming increasingly prevalent in patients who exhibit a progressive decline in kidney function. However, the…”
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  11. 11

    Hypoparathyroidism concomitant with macrothrombocytopenia in an elderly woman with 22q11.2 deletion syndrome by Yang, Hsiu-Chien, Lin, Shih-Hua, Wu, Yi-Ying, Sung, Chih-Chien

    Published in Platelets (Edinburgh) (01-11-2018)
    “…We describe the case of a 62-year-old woman with schizophrenia and intellectual disability, who presented with intermittent muscle cramping for 2 weeks. A…”
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  12. 12

    Clinical analysis for osmotic demyelination syndrome in patients with chronic hyponatremia by Hsi-Chih Chen, Chih-Chien Sung, Yi-Chang Lin, Lin-Chien Chan, Shih-Hua Lin

    Published in Journal of Medical Sciences (01-09-2022)
    “…Background: Although osmotic demyelination syndrome (ODS) has been well known to be associated with a rapid correction of sodium (Na+) in patients with chronic…”
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  13. 13

    Allele-specific RT-PCR for the rapid detection of recurrent SLC12A3 mutations for Gitelman syndrome by Yan, Ming-Tso, Yang, Sung-Sen, Tseng, Min-Hua, Cheng, Chih-Jen, Tsai, Jeng-Daw, Sung, Chih-Chien, Hsu, Yu-Juei, Lin, Shih-Hua

    Published in Npj genomic medicine (13-08-2021)
    “…Recurrent mutations in the SLC12A3 gene responsible for autosomal recessive Gitelman syndrome (GS) are frequently reported, but the exact prevalence is…”
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  14. 14

    Acute kidney disease following COVID-19 vaccination: a single-center retrospective study by Chen, Chien-Chou, Yang, Sung-Sen, Hsu, Yu-Juei, Sung, Chih-Chien, Chu, Pauling, Wu, Chia-Chao, Hsu, Shun-Neng, Wang, Han-En, Lee, Ding-Jie, Lin, Shih-Hua

    Published in Frontiers in medicine (22-05-2023)
    “…Rare cases of or relapsed kidney diseases associated with vaccination against coronavirus disease 2019 (COVID-19) have been increasingly reported. The aim of…”
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  15. 15

    Urinary Extracellular Vesicles for Renal Tubular Transporters Expression in Patients With Gitelman Syndrome by Sung, Chih-Chien, Chen, Min-Hsiu, Lin, Yi-Chang, Lin, Yu-Chun, Lin, Yi-Jia, Yang, Sung-Sen, Lin, Shih-Hua

    Published in Frontiers in medicine (09-06-2021)
    “…Background: The utility of urinary extracellular vesicles (uEVs) to faithfully represent the changes of renal tubular protein expression remains unclear. We…”
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  16. 16

    Etiologic and Therapeutic Analysis in Patients with Hypokalemic Nonperiodic Paralysis by Sung, Chih-Chien, MD, Cheng, Chih-Jen, MD, PhD, Chiang, Wen-Fang, MD, Chau, Tom, MD, Hsu, Yu-Juei, MD, PhD, Yang, Sung-Sen, MD, PhD, Lin, Shih-Hua, MD

    Published in The American journal of medicine (01-03-2015)
    “…Abstract Background Hypokalemic nonperiodic paralysis represents a group of heterogeneous disorders with a large potassium (K+ ) deficit. Rapid diagnosis of…”
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  17. 17

    Nonobstructive Hydronephrosis with Secondary Polycythemia by Sung, Chih-Chien, Lin, Shih-Hua

    Published in The New England journal of medicine (07-07-2011)
    “…A 34-year-old nonsmoking man was referred for evaluation of a history of polycythemia that required monthly phlebotomy. His medical history was significant for…”
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  18. 18

    NSC828779 Alleviates Renal Tubulointerstitial Lesions Involving Interleukin-36 Signaling in Mice by Yang, Shin-Ruen, Hung, Szu-Chun, Chu, Lichieh Julie, Hua, Kuo-Feng, Wei, Chyou-Wei, Tsai, I-Lin, Kao, Chih-Chin, Sung, Chih-Chien, Chu, Pauling, Wu, Chung-Yao, Chen, Ann, Wu, Alexander T H, Liu, Feng-Cheng, Huang, Hsu-Shan, Ka, Shuk-Man

    Published in Cells (Basel, Switzerland) (06-11-2021)
    “…Renal tubulointerstitial lesions (TILs), a common pathologic hallmark of chronic kidney disease that evolves to end-stage renal disease, is characterized by…”
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  19. 19

    Genotype and Phenotype Analysis of Patients With Sporadic Periodic Paralysis by Sung, Chih-Chien, MD, Cheng, Chih-Jen, MD, Lo, Yi-Fen, PhD, Lin, Mei-Shan, PhD, Yang, Sung-Sen, MD, PhD, Lin, Shih-Hua, MD, Hsu, Yu-Chuan, MD

    “…Abstract Introduction Sporadic periodic paralysis (SPP), the second leading cause of hypokalemic periodic paralysis (HPP) in Asia, has a presentation similar…”
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  20. 20

    R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura by Sung, Chih-Chien, Lin, Shih-Hua, Chao, Tai-Kuang, Chen, Yeu-Chin

    “…May-Hegglin anomaly (MHA) is a rare autosomal dominant disorder characterized by the triad of thrombocytopenia, giant platelets, and inclusion bodies in…”
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