Search Results - "LUNDQUIST, Andrew L"

Optimal management of bone mineral disorders in chronic kidney disease and end stage renal disease by Lundquist, Andrew L, Nigwekar, Sagar U

“…PURPOSE OF REVIEWThe review summarizes recent studies on chronic kidney disease–mineral bone disorders, with a focus on new developments in disease management…”
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Ectopic germinal center and megalin defect in primary Sjogren syndrome with renal Fanconi syndrome by Wang, Jing, Wen, Yubing, Zhou, Mengyu, Shi, Xiaoxiao, Jiang, Lanping, Li, Mingxi, Yu, Yang, Li, Xuemei, Li, Xuewang, Zhang, Wen, Lundquist, Andrew L, Chen, Limeng

“…This study reports the clinical and pathological features of 12 cases of primary Sjogren syndrome (pSS) with renal involvement presenting with proximal tubular…”
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A pragmatic approach to selective genetic testing in kidney transplant candidates by Nissaisorakarn, Pitchaphon, Fadakar, Paul K, Safa, Kassem, Lundquist, Andrew L, Riella, Cristian V, Riella, Leonardo V

“…Advances in the field of genetic testing have spurred its use in transplantation. Potential benefits of genetic testing in transplant nephrology include…”
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KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome by CROTTI, Lia, LUNDQUIST, Andrew L, SCHWARTZ, Peter J, INSOLIA, Roberto, PEDRAZZINI, Matteo, FERRANDI, Chiara, DE FERRARI, Gaetano M, VICENTINI, Alessandro, PING YANG, RODEN, Dan M, GEORGE, Alfred L

“…Clinical heterogeneity among patients with long-QT syndrome (LQTS) sharing the same disease-causing mutation is usually attributed to variable penetrance. One…”
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Reduced guanidinoacetate in plasma of patients with autosomal dominant Fanconi syndrome due to heterozygous P341L GATM variant and study of organoids towards treatment by Portales‐Castillo, Ignacio, Singal, Rhea, Ambrose, Anastasia, Song, Jong Hee, Son, Minsoo, Goo, Young Ah, Zhou, Wen, Traum, Avram Z., Coler‐Reilly, Ariella, Humphreys, Benjamin D., Civitelli, Roberto, Jüppner, Harald, Lundquist, Andrew L., Seres, Peter, Allegretti, Andrew S., Mercimek‐Andrews, Saadet

“…Autosomal dominant Fanconi syndrome due to a GATM variant (GATM‐FS), causes accumulation of misfolded arginine‐glycine amidinotransferase (AGAT) in proximal…”
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Video Images about Decisions for Ethical Outcomes in Kidney Disease (VIDEO-KD): the study protocol for a multi-centre randomised controlled trial by Eneanya, Nwamaka D, Lakin, Joshua R, Paasche-Orlow, Michael K, Lindvall, Charlotta, Moseley, Edward T, Henault, Lori, Hanchate, Amresh D, Mandel, Ernest I, Wong, Susan P Y, Zupanc, Sophia N, Davis, Aretha Delight, El-Jawahri, Areej, Quintiliani, Lisa M, Chang, Yuchiao, Waikar, Sushrut S, Bansal, Amar D, Schell, Jane O, Lundquist, Andrew L, Tamura, Manjula Kurella, Yu, Margaret K, Unruh, Mark L, Argyropoulos, Christos, Germain, Michael J, Volandes, Angelo

“…IntroductionOlder patients with advanced chronic kidney disease (CKD) often are inadequately prepared to make informed decisions about treatments including…”
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Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population by BRINK, Paul A, CROTTI, Lia, SPAZZOLINI, Carla, LUNDQUIST, Andrew L, RODEN, Dan M, GEORGE, Alfred L, SCHWARTZ, Peter J, CORFIELD, Valerie, GOOSEN, Althea, DURRHEIM, Glenda, HEDLEY, Paula, HERADIEN, Marshall, GELDENHUYS, Gerhard, VANOLI, Emilio, BACCHINI, Sara

“…In the congenital long-QT syndrome (LQTS), there can be a marked phenotypic heterogeneity. Founder effects, by which many individuals share a mutation…”
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Treatment of hepatitis C virus–associated mixed cryoglobulinemia with direct‐acting antiviral agents by Sise, Meghan E., Bloom, Allyson K., Wisocky, Jessica, Lin, Ming V., Gustafson, Jenna L., Lundquist, Andrew L., Steele, David, Thiim, Michael, Williams, Winfred W., Hashemi, Nikroo, Kim, Arthur Y., Thadhani, Ravi, Chung, Raymond T.

“…Hepatitis C virus (HCV) is the most common cause of mixed cryoglobulinemia syndrome (MCS). The efficacy and safety of all‐oral direct‐acting antiviral (DAA)…”
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Hybrid Assemblies of ATP-Sensitive K⁺ Channels Determine Their Muscle-Type-Dependent Biophysical and Pharmacological Properties by Tricarico, Domenico, Mele, Antonietta, Lundquist, Andrew L., Desai, Reshma R., George, Alfred L., Camerino, Diana Conte

“…ATP-sensitive K⁺ channels ($K_{ATP}$) are an octameric complex of inwardly rectifying K⁺ channels (Kir6.1 and Kir6.2) and sulfonylurea receptors (SUR1 and…”
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Lupus-like Immune Complex-mediated Glomerulonephritis in Patients with Hepatitis C Virus Infection Treated with Oral, Interferon-free, Direct-acting Antiviral Therapy by Sise, Meghan E, Wisocky, Jessica, Rosales, Ivy A, Chute, Donald, Holmes, Jacinta A, Corapi, Kristin M, Babitt, Jodie L, Tangren, Jessica S, Hashemi, Nikroo, Lundquist, Andrew L, Williams, Winfred W, Mount, David B, Andersson, Karin L, Rennke, Helmut G, Smith, R Neal, Colvin, Robert, Thadhani, Ravi I, Chung, Raymond T

“…Novel, all-oral interferon-free direct-acting antiviral agents have revolutionized the management of hepatitis C virus (HCV) infection by producing exceptional…”
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Case 30-2020: A 54-Year-Old Man with Sudden Cardiac Arrest by Edelman, Elazer R, Butala, Neel M, Avery, Laura L, Lundquist, Andrew L, Dighe, Anand S

“…A 54-year-old man was evaluated at the hospital after cardiac arrest associated with ventricular fibrillation. The patient had been in a fast-food restaurant…”
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Case 13-2020: A 29-Year-Old Man with High Blood Pressure, Renal Insufficiency, and Hematuria by Lundquist, Andrew L, Kalim, Sahir, Mojtahed, Amirkasra, Tomaszewski, Kristen J

“…A 29-year-old man was evaluated because of hypertension, renal insufficiency, and hematuria. He had a blood pressure of 160/102 mm Hg, a urea nitrogen level of…”
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Expression and transcriptional control of human KCNE genes by Lundquist, Andrew L., Turner, Candice L., Ballester, Leomar Y., George, Alfred L.

“…Potassium channels are essential for a variety of cellular processes ranging from membrane excitability to cellular proliferation. The KCNE genes ( KCNE1– 5)…”
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Case 38-2020: A 52-Year-Old Man with Cancer and Acute Hypoxemia by Marinacci, Lucas X, Simeone, F. Joseph, Lundquist, Andrew L, Kuter, David J, Mahowald, Grace K

“…A 52-year-old man with back pain was admitted to the hospital with a vertebral mass, multiple lytic bone lesions, and severe hypercalcemia. MRI showed an…”
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Filter clotting with continuous renal replacement therapy in COVID-19 by Endres, Paul, Rosovsky, Rachel, Zhao, Sophia, Krinsky, Scott, Percy, Shananssa, Kamal, Omer, Roberts, Russel J., Lopez, Natasha, Sise, Meghan E., Steele, David J. R., Lundquist, Andrew L., Rhee, Eugene P., Hibbert, Kathryn A., Hardin, C. Corey, Mc Causland, Finnian R., Czarnecki, Peter G., Mutter, Walter, Tolkoff-Rubin, Nina, Allegretti, Andrew S.

“…Coronavirus disease 2019 (COVID-19) appears to be associated with increased arterial and venous thromboembolic disease. These presumed abnormalities in…”
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Assessment of Interobserver Reliability of Nephrologist Examination of Urine Sediment by Palsson, Ragnar, Colona, Mia R, Hoenig, Melanie P, Lundquist, Andrew L, Novak, James E, Perazella, Mark A, Waikar, Sushrut S

“…Urine sediment microscopy is commonly performed during the evaluation of kidney disease. Interobserver reliability of nephrologists' urine sediment examination…”
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From Theory to Reality: Establishing a Successful Kidney Genetics Clinic in the Outpatient Setting by Lundquist, Andrew L, Pelletier, Renee C, Leonard, Courtney E, Williams, Winfred W, Armstrong, Katrina A, Rehm, Heidi L, Rhee, Eugene P

“…Genetic testing in nephrology is increasingly described in the literature and several groups have suggested significant clinical benefit. However, studies to…”
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Serum sickness following rabbit antithymocyte‐globulin induction in a liver transplant recipient: Case report and literature review by Lundquist, Andrew L., Chari, Ravi S., Wood, James H., Miller, Geraldine G., Schaefer, Heidi M., Raiford, David S., Wright, Kelly J., Gorden, D. Lee

“…Thymoglobulin® (Genzyme, Cambridge, MA) is an antithymocyte globulin preparation used for induction immunosuppression therapy in solid organ transplantation…”
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Reduced expression of Kir6.2/SUR2A subunits explains KATP deficiency in K+ -depleted rats by Tricarico, Domenico, Mele, Antonietta, Liss, Birgit, Ashcroft, Frances M, Lundquist, Andrew L, Desai, Reshma R, George, Alfred L, Conte Camerino, Diana

“…Abstract We investigated on the mechanism responsible for the reduced ATP-sensitive K+ (KATP ) channel activity recorded from skeletal muscle of K+ -depleted…”
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Autosomal Dominant Fanconi Syndrome and CKD Associated With Glycine Amidinotransferase Mutation: A Rare Genetic Syndrome: SA-PO528 by Portales Castillo, Ignacio A., Hanna, Patrick, Lundquist, Andrew L., Jüppner, Harald, Traum, Avi, Allegretti, Andrew S.

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