Search Results - "Cramer, Carl H"

Thrombotic Microangiopathy Care Pathway: A Consensus Statement for the Mayo Clinic Complement Alternative Pathway-Thrombotic Microangiopathy (CAP-TMA) Disease-Oriented Group by Go, Ronald S., MD, Winters, Jeffrey L., MD, Leung, Nelson, MD, Murray, David L., MD, PhD, Willrich, Maria A., PhD, Abraham, Roshini S., PhD, Amer, Hatem, MD, Hogan, William J., MBBCh, Marshall, Ariela L., MD, Sethi, Sanjeev, MD, PhD, Tran, Cheryl L., MD, Chen, Dong, MD, PhD, Pruthi, Rajiv K., MBBS, Ashrani, Aneel A., MD, MS, Fervenza, Fernando C., MD, PhD, Cramer, Carl H., MD, Rodriguez, Vilmarie, MD, Wolanskyj, Alexandra P., MD, Thomé, Stephan D., MD, Hook, C. Christopher, MD

“…Abstract Thrombotic microangiopathies (TMAs) comprise a heterogeneous set of conditions linked by a common histopathologic finding of endothelial damage…”
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Negative Staining for COL4A5 Correlates With Worse Prognosis and More Severe Ultrastructural Alterations in Males With Alport Syndrome by Said, Samar M, Fidler, Mary E, Valeri, Anthony M, McCann, Brooke, Fiedler, Wade, Cornell, Lynn D, Alexander, Mariam Priya, Alkhunaizi, Ahmed M, Sullivan, Anne, Cramer, Carl H, Hogan, Marie C, Nasr, Samih H

“…Alport syndrome (AS) is a genetic disorder characterized by progressive hematuric nephropathy with or without sensorineural hearing loss and ocular lesions…”
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Immune response to rabies vaccination in pediatric transplant patients by Cramer II, Carl H., Shieck, Victoria, Thomas, Susan E., Kershaw, David B., Magee, John C., Lopez, M. James

“…:  Children have become engaged in a wider variety of activities as the success of solid organ transplantation has improved. These activities can result in…”
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Feasibility Study of Vascularized Composite Urinary Bladder Allograft Transplantation in a Cadaver Model by Gargollo, Patricio C, Ahmed, Mohamed E, Prieto, Mikel, Butaney, Mohit, Cramer, Carl H, Joshi, Vidhu, Heimbach, Julie K, Granberg, Candace F

“…The purpose of this study was to establish the feasibility of performing a urinary bladder vascularized composite allograft transplantation for either bladder…”
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A Framework for Outpatient Infusion of Antispike Monoclonal Antibodies to High-Risk Patients with Mild-to-Moderate Coronavirus Disease-19: The Mayo Clinic Model by Razonable, Raymund R, Aloia, Nicole C E, Anderson, Ryan J, Anil, Gokhan, Arndt, Lori L, Arndt, Richard F, Ausman, Sara E, Bell, Sarah J, Bierle, Dennis M, Billings, Marcie L, Bishop, Rachel K, Cramer, Carl H, Culbertson, Tracy L, Dababneh, Ala S, Derr, Amber N, Epps, Kevin, Flaker, Susan M, Ganesh, Ravindra, Gilmer, Mary A, Urena, Eric Gomez, Gulden, Christopher R, Haack, Tamara L, Hanson, Sara N, Herzog, Jenna R, Heyliger, Alexander, Hokanson, Lex D, Hopkins, Laura H, Horecki, Richard J, Krishna, Bipinchandra Hirisave, Huskins, W Charles, Jackson, Tammy A, Johnson, Ryan R, Jorgenson, Betty, Kudrna, Cory, Kennedy, Brian D, Klingsporn, Mary K, Kottke, Brian, Larsen, Jennifer J, Lessard, Sarah R, Lutwick, Larry I, Malone, 3rd, Edward J, Matoush, Jennifer A, Micallef, Ivana N, Moehnke, Darcie E, Mohamed, Muhanad, Ness, Colleena N, Olson, Shelly M, Orenstein, Robert, Palraj, Raj, Patel, Janki, Paulson, Damian J, Phelan, David, Peinovich, Margaret T, Ramsey, Wilford L, Rau-Kane, Taunya J, Reid, Kevin I, Reinschmidt, Karen J, Seville, Maria Teresa, Skold, Erin C, Smith, Jill M, Speicher, Leigh L, Spielman, Laurie A, Springer, Donna J, Sweeten, Perry W, Tempelis, Jennifer M, Tulledge-Scheitel, Sidna, Vergidis, Paschalis, Whipple, Daniel C, Wilker, Caroline G, Destro Borgen, Molly J

“…The administration of spike monoclonal antibody treatment to patients with mild to moderate COVID-19 is very challenging. This article summarizes essential…”
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New-onset cough and fever in a toddler with stage 5 chronic kidney disease: Answers by Petri, Cassandra A., Perez, Yalile, Heidenreich, Leah S., Cramer, Carl H., Olson, Timothy M., Hull, Nathan C., Hanna, Christian

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New-onset cough and fever in a toddler with stage 5 chronic kidney disease: Questions by Petri, Cassandra A., Perez, Yalile, Heidenreich, Leah S., Cramer, Carl H., Olson, Timothy M., Hull, Nathan C., Hanna, Christian

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Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations by Hoskins, Bethan E., Cramer, Carl H., Tasic, Velibor, Kehinde, Elijah O., Ashraf, Shazia, Bogdanovic, Radovan, Hoefele, Julia, Pohl, Martin, Hildebrandt, Friedhelm

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Growth hormone deficiency in a child with branchio‐oto‐renal spectrum disorder: Clinical evidence of EYA1 in pituitary development and a recommendation for pituitary function surveillance by Muthusamy, Karthik, Hanna, Christian, Johnson, Derek R., Cramer, Carl H., Tebben, Peter J., Libi, Sharon E., Poling, Gayla L., Lanpher, Brendan C., Morava, Eva, Schimmenti, Lisa A.

“…Branchio‐oto‐renal spectrum disorder (BORSD) is a rare autosomal dominant condition characterized by ear abnormalities with hard of hearing/deafness, second…”
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Transcription Factor SIX5 Is Mutated in Patients with Branchio-Oto-Renal Syndrome by Hoskins, Bethan E., Cramer, Carl H., Silvius, Derek, Zou, Dan, Raymond, Richard M., Orten, Dana J., Kimberling, William J., Smith, Richard J.H., Weil, Dominique, Petit, Christine, Otto, Edgar A., Xu, Pin-Xian, Hildebrandt, Friedhelm

“…Branchio-oto-renal syndrome (BOR) is an autosomal dominant developmental disorder characterized by the association of branchial arch defects, hearing loss, and…”
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Clinical presentation and outcome in a cohort of paediatric patients with membranous lupus nephritis by Cramer, Carl H., Mills, Michelle, Valentini, Rudolph P., Smoyer, William E., Haftel, Hillary, Brophy, Patrick D.

“…Background. Membranous glomerulopathy accounts for 28% of the biopsy-proven systemic lupus erythematosus nephritis in paediatric patients at the time of first…”
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Using a Modified CPD Blood Bag to Store Blood from either ECMO or RRT Circuit Blood in Pediatric Patients by Neal, James R, Friedrich, Tammy P, Schears, Gregory J, Cramer, Carl H

“…By adapting a citrate phosphate dextrose (CPD) whole blood storage bag, residual blood from a renal replacement therapy (RRT) circuit can be saved in pediatric…”
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Discontinuation of dialysis with eculizumab therapy in a pediatric patient with dense deposit disease by Tran, Cheryl L., Sethi, Sanjeev, Murray, David, Cramer, Carl H., Sas, David J., Willrich, Maria, Smith, Richard J., Fervenza, Fernando C.

“…Background Dense deposit disease (DDD) is a rare glomerular disease caused by an uncontrolled activation of the alternative complement pathway leading to…”
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Abdominal Pain, Flank Pain, Blurry Vision, and Lower Extremity Weakness in a 16‐Year‐Old Female by Mao, Michael A., Wu, YiFan, Fidler, Mary E., Cramer, Carl H., Bower, Thomas C., Qian, Qi

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Charcoal hemoperfusion in the treatment of medically refractory pruritus in cholestatic liver disease by Kittanamongkolchai, Wonngarm, El-Zoghby, Ziad M., Eileen Hay, J., Wiesner, Russell H., Kamath, Patrick S., LaRusso, Nicholas F., Watt, Kymberly D., Cramer, Carl H., Leung, Nelson

“…Background Pruritus is a distressing symptom in a considerable proportion of cholestatic patients and a few of them do not respond to conventional treatment…”
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Empiric switch from calcineurin inhibitor to sirolimus-based immunosuppression in pediatric heart transplantation recipients by Loar, Robert W., Driscoll, David J., Kushwaha, Sudhir S., Cramer, Carl H., O'Leary, Patrick W., Daly, Richard C., Mauriello, Daniel A., Johnson, Jonathan N.

“…Sirolimus is used in heart transplant patients with CAV and CNI‐induced nephropathy. However, little is known regarding the tolerability, rejection rate, and…”
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Correlation of Blood Pressure Readings From 6‐Hour Intervals With the Daytime Period of 24‐Hour Ambulatory Blood Pressure Monitoring in Pediatric Patients by King‐Schultz, Leslie, Weaver, Amy L., Cramer, Carl H.

“…J Clin Hypertens (Greenwich). 2012; 14:396–400. ©2012 Wiley Periodicals, Inc. Shorter‐interval (6‐hour) ambulatory blood pressure monitoring (ABPM) has been…”
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11 year old with proximal tubule subnuclear vacuoles by Juskewitch, Justin E., M.D. Ph.D, Cramer, Carl H., M.D, Alexander, Mariam P., M.D

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Gastrointestinal Symptoms of Henoch‐Schönlein Purpura Treated with Mycophenolate Mofetil by Martin, Scott, Cramer, Carl H., Heikenen, Janice, Gitomer, Jeremy J.

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Genetic Insights into Pediatric Polycystic Kidney Disease: FR-PO674 by Hanna, Christian, Yang, Hana, Schauer, Rachel S., Sas, David J., Tran, Cheryl L., Cramer, Carl H., Harris, Peter C.

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