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Csaba P. Kovesdy

Researcher at University of Tennessee Health Science Center

Publications -  649
Citations -  41377

Csaba P. Kovesdy is an academic researcher from University of Tennessee Health Science Center. The author has contributed to research in topics: Kidney disease & Dialysis. The author has an hindex of 92, co-authored 605 publications receiving 31462 citations. Previous affiliations of Csaba P. Kovesdy include University of California, Irvine & Semmelweis University.

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Burnt-Out Diabetes: Impact of Chronic Kidney Disease Progression on the Natural Course of Diabetes Mellitus

TL;DR: Studying this condition and its potential causes and consequences may lead to a better understanding of the pathophysiology of metabolic syndrome and diabetes mellitus in the CKD population and in many other individuals with chronic disease states associated with wasting syndrome that can confound the natural history of diabetes.
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Thyroid functional disease: an under-recognized cardiovascular risk factor in kidney disease patients

TL;DR: Mechanisms by which hypothyroidism adversely affects cardiovascular health are discussed; the prognostic implications of hypothyrodesis, thyroid hormone alterations and exogenous thyroid hormone replacement in CKD and ESRD are examined; and areas of uncertainty related to the interplay between hypothyrogenism, cardiovascular disease and kidney disease requiring further investigation are identified.
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Controversies in optimal anemia management: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Conference.

Jodie L. Babitt, +59 more
- 01 Jun 2021 - 
TL;DR: In chronic kidney disease, anemia and disordered iron homeostasis are prevalent and associated with significant adverse consequences as discussed by the authors, and new data have accrued from basic research, epidemiological studies, and randomized trials that warrant a re-examination of previous recommendations.
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Constipation and Incident CKD

TL;DR: It is found that absent, mild, or moderate/severe constipation associate with higher risk of incident CKD and ESRD and with progressive eGFR decline, independent of known risk factors.