Results 21 to 30 of about 8,432 (181)

Anaesthesia for laparoscopic cholecystectomy in Bartter′s syndrome

Indian Journal of Anaesthesia, 2010
Bartter′s syndrome is a rare inherited anamoly with defect in the thick segment of the ascending limb of the loop of Henle, with reduced reabsorption of potassium.
Bala S Bhaskar, G V Rao, Sanjeev B Joshi, S K Arun, S K Ajay   +4 more
doaj   +1 more source

A predictive model for the quantitative assessment of intratubular urodynamics during the creation of osmotic (electrochemical) gradient by the loops of Henle in the renal parenchyma

Кубанский научный медицинский вестник
Background. Described more than half a century ago, the countercurrent multiplication mechanism in the loop of Henle remains hypothetical; it suggests that tubular flow is significantly influenced by physicochemical processes that have yet to be ...
A. S. Tatevosyan, A. V. Bunyakin, S. N. Alekseenko, Z. O. Katani, A. A. Yuldashev, B. A. Ismatov   +5 more
doaj   +1 more source

A Case of Adult onset Bartter Syndrome with Nephrocalcinosis [PDF]

Kosin Medical Journal, 2014
Bartter syndrome is a renal tubular defect in electrolyte transport characterized by hypokalemia, metabolic alkalosis, hyperreninemia, hyperaldosteronism, normal blood pressure, and other clinical symptoms.
Min Gyu Park, Tae Won Lim, Hee Taek Oh, Seung Un Song, Dong Heo, Hark Rim   +5 more
doaj   +1 more source

TGR5 expression in normal kidney and renal neoplasms

Diagnostic Pathology, 2018
Background The G protein-coupled bile acid receptor (TGR5) is a cell surface receptor which induces the production of intracellular cAMP and promotes epithelial-mesenchymal transition in gastric cancer cell lines.
Chaohui Lisa Zhao, Ali Amin, Yiang Hui, Dongfang Yang, Weibiao Cao   +4 more
doaj   +1 more source

Single-cell transcriptome analysis of a rat model of bilateral renal ischemia-reperfusion injury

Biochemistry and Biophysics Reports, 2023
Ischemia-reperfusion injury (IRI) causes massive tissue damage. Renal IRI is the most common type of acute renal injury, and the defects caused by it may progress to chronic kidney disease (CKD).
Ayumu Taniguchi, Kazuya Miyashita, Shota Fukae, Ryo Tanaka, Mami Nishida, Tomomi Kitayama, Yuya Ouchi, Takashi Shimbo, Shigeaki Nakazawa, Kazuaki Yamanaka, Ryoichi Imamura, Katsuto Tamai, Norio Nonomura   +12 more
doaj   +1 more source

Autosomal dominant hypocalcemia with Bartter syndrome due to a novel activating mutation of calcium sensing receptor, Y829C [PDF]

Korean Journal of Pediatrics, 2015
The calcium sensing receptor (CaSR) plays an important role in calcium homeostasis. Activating mutations of CaSR cause autosomal dominant hypocalcemia by affecting parathyroid hormone secretion in parathyroid gland and calcium resorption in kidney.
Keun Hee Choi, Choong Ho Shin, Sei Won Yang, Hae Il Cheong   +3 more
doaj   +1 more source

Advances in the correlation of uromodulin and UMOD gene with chronic kidney disease [PDF]

Jichu yixue yu linchuang, 2020
Uromodulin, also known as Tamm-Horsfal protein, is the most abundant protein in normal urine. It is exclusively secreted by renal tubular epithelial cells in thick ascending limb (TAL) of the Henle loop.
YOU Rui-lian, XU Lu-bin, CHEN Li-meng
doaj  

Modeling the Steady-State Effects of Mean Arterial Pressure on the Kidneys

IEEE Open Journal of Engineering in Medicine and Biology, 2021
Goal: We describe the relationship between mean arterial pressure (MAP) and glomerular filtration rate (GFR) since therapies affecting MAP can have large effects on kidney function.
Benjamin J. Czerwin, Sandip Patel, Caitlyn M. Chiofolo, Jiayao Yuan, Nicolas W. Chbat   +4 more
doaj   +1 more source

Blood pressure effects of SGLT2 inhibitors and GLP‐1 receptor agonists: Mechanisms, trial evidence and Real‐world data

British Journal of Clinical Pharmacology, EarlyView.
SGLT2 inhibitors and GLP‐1 receptor agonists modestly lower blood pressure across diverse patient populations, including those without diabetes. These effects appear largely independent of glycaemic control and offer additive value in high‐risk patients with overlapping comorbidities.
Andrej Belančić, Yusuf Ziya Sener, Marijana Vučković, Joseph Edgar Blais, Almir Fajkić, Emina Sher, Mislav Radić, Josipa Radić   +7 more
wiley   +1 more source

Enfermedades renales que cursan con hipomagnesemia. Comentarios acerca de una nueva tubulopatía hipomagnesémica de origen genético

Nefrología
Resumen: Las enfermedades renales que cursan con hipomagnesemia son un grupo complejo y variopinto de tubulopatías producidas por mutaciones en genes que codifican proteínas que se expresan en la rama gruesa ascendente del asa de Henle y en el túbulo ...
Víctor M. Garcia-Nieto, Félix Claverie-Martin, Teresa Moraleda-Mesa, Ana Perdomo-Ramírez, Gloria Ma Fraga-Rodríguez, María Isabel Luis-Yanes, Elena Ramos-Trujillo   +6 more
doaj   +1 more source