Zobrazeno 1 - 10
of 380
pro vyhledávání: '"David S. Goldfarb"'
Autor:
Lilia R. Lukowsky, Claudia Der-Martirosian, Heather Northcraft, Kamyar Kalantar-Zadeh, David S. Goldfarb, Aram Dobalian
Publikováno v:
Vaccines, Vol 12, Iss 2, p 146 (2024)
Background: There are knowledge gaps about factors associated with acute kidney injury (AKI) among COVID-19 patients. To examine AKI predictors among COVID-19 patients, a retrospective longitudinal cohort study was conducted between January 2020 and
Externí odkaz:
https://doaj.org/article/3e05210fb49b4479adc966233d85847c
Autor:
Sarah M. Azer, David S. Goldfarb
Publikováno v:
Healthcare, Vol 11, Iss 5, p 674 (2023)
Cystinuria is the most common genetic cause of recurrent kidney stones. As the result of a genetic defect in proximal tubular reabsorption of filtered cystine, increased urine levels of the poorly soluble amino acid result in recurrent cystine nephro
Externí odkaz:
https://doaj.org/article/b69d6f7376104d10b1c39aed13a20c6d
Autor:
Kyriaki Stamatelou, David S. Goldfarb
Publikováno v:
Healthcare, Vol 11, Iss 3, p 424 (2023)
In the past two decades, major breakthroughs that improve our understanding of the pathophysiology and therapy of kidney stones (KS) have been lacking. The disease continues to be challenging for patients, physicians, and healthcare systems alike. In
Externí odkaz:
https://doaj.org/article/4336edb5e2b842a1b0bc15a884b092d2
Publikováno v:
Kidney International Reports, Vol 4, Iss 4, Pp 535-540 (2019)
Background: Nephrolithiasis is a complex phenotype influenced by both genetic and environmental factors. Previously we found a genetic component to stone disease using a sample of male twin pairs. We now report on the genetic contribution to stones i
Externí odkaz:
https://doaj.org/article/bc2235b721464832b10fe854d3eefeaa
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-9 (2019)
Abstract Background Volume overload and depletion both lead to high morbidity and mortality. Achieving euvolemia is a challenge in patients with end stage kidney disease on hemodialysis (HD). Blood volume analysis (BVA) uses radiolabeled albumin to d
Externí odkaz:
https://doaj.org/article/6d97ca3b58934ec5900cd4b1fcec660a
Publikováno v:
Clinical Practice and Cases in Emergency Medicine, Vol 5, Iss 2 (2021)
Introduction: The term “lactic acidosis” reinforces the misconception that lactate contributes to acidemia. Although it is common to discover an anion gap acidosis with a concomitant elevated lactate concentration, the two are not mutually depend
Externí odkaz:
https://doaj.org/article/14e644335e2e48a0a7e4be2774351490
Autor:
Lilia R. Lukowsky, Aram Dobalian, David S. Goldfarb, Kamyar Kalantar-Zadeh, Claudia Der-Martirosian
Publikováno v:
Journal of Primary Care & Community Health, Vol 10 (2019)
Introduction: This study examines the use of dialysis services by end-stage renal disease (ESRD) patients following the Superstorm Sandy–related, months-long closure of the New York campus of the US Department of Veterans Affairs (VA) New York Harb
Externí odkaz:
https://doaj.org/article/62bfd010b7224892a19e9e1aeaf5c433
Autor:
William E. Haley, El-Sayed H. Ibrahim, Mingliang Qu, Joseph G. Cernigliaro, David S. Goldfarb, Cynthia H. McCollough
Publikováno v:
Case Reports in Radiology, Vol 2015 (2015)
Dual-energy computed tomography (DECT) has recently been suggested as the imaging modality of choice for kidney stones due to its ability to provide information on stone composition. Standard postprocessing of the dual-energy images accurately identi
Externí odkaz:
https://doaj.org/article/f20b4ff014494f1d8ac86d230ec061e9
Autor:
Max Xiangtian Kong, Christopher Hale, Antonio Subietas-Mayol, Peng Lee, Nicholas D. Cassai, Gerald McRae, David S. Goldfarb, Ming Zhou, Rosemary Wieczorek
Publikováno v:
Rare Tumors, Vol 5, Iss 4, Pp e57-e57 (2013)
Tubulocystic renal cell carcinoma (TC-RCC) is a rare renal tumor composed of well-differentiated tubules and cysts lined by neoplastic cells with eosinophilic cytoplasm and prominent nucleoli. The origin of the tumor cells is still controversial. TC-
Externí odkaz:
https://doaj.org/article/9410fcbf952841c29591b57ee241e59f
Publikováno v:
Case Reports in Nephrology, Vol 2013 (2013)
Introduction. Minimal Change Disease (MCD) is the most common cause of nephrotic syndrome in children, while IgA nephropathy is the most common cause of glomerulonephritis worldwide. MCD is responsive to glucocorticoids, while the role of steroids in
Externí odkaz:
https://doaj.org/article/20522317a1ad4dfda06bc64d8a24b70e