Search Results - "Sung, Chih‐Chien"
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‘Aquaporin‐omics’: mechanisms of aquaporin‐2 loss in polyuric disorders
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
Icodextrin‐induced acute generalized exanthematous pustulosis in a patient with peritoneal dialysis
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
Role of Vitamin D in Insulin Resistance
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
Independent Determinants of Appetite Impairment among Patients with Stage 3 or Higher Chronic Kidney Disease: A Prospective Study
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
A young man with secondary adrenal insufficiency due to empty sella syndrome
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
Phytobezoar-induced small bowel obstruction in an elderly patient undergoing dialysis: a case report
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
Novel CNNM2 Mutation Responsible for Autosomal-Dominant Hypomagnesemia With Seizure
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
Identification and characterization of a novel CASR mutation causing familial hypocalciuric hypercalcemia
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
Insulin Resistance in Patients with Chronic Kidney Disease
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
Association of Serum Phosphate with Low Handgrip Strength in Patients with Advanced Chronic Kidney Disease
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
Hypoparathyroidism concomitant with macrothrombocytopenia in an elderly woman with 22q11.2 deletion syndrome
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
Clinical analysis for osmotic demyelination syndrome in patients with chronic hyponatremia
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
Allele-specific RT-PCR for the rapid detection of recurrent SLC12A3 mutations for Gitelman syndrome
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
Acute kidney disease following COVID-19 vaccination: a single-center retrospective study
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
Urinary Extracellular Vesicles for Renal Tubular Transporters Expression in Patients With Gitelman Syndrome
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
Etiologic and Therapeutic Analysis in Patients with Hypokalemic Nonperiodic Paralysis
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
Nonobstructive Hydronephrosis with Secondary Polycythemia
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
NSC828779 Alleviates Renal Tubulointerstitial Lesions Involving Interleukin-36 Signaling in Mice
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
Genotype and Phenotype Analysis of Patients With Sporadic Periodic Paralysis
Published in The American journal of the medical sciences (01-04-2012)“…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
R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura
Published in Journal of the Formosan Medical Association (01-01-2014)“…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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