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201 results on '"Zager, Philip G"'

1. Personalised cooler dialysate for patients receiving maintenance haemodialysis (MyTEMP): a pragmatic, cluster-randomised trial

Author

Garg, Amit X, Al-Jaishi, Ahmed A, Dixon, Stephanie N, Sontrop, Jessica M, Anderson, Sierra J, Bagga, Amit, Benjamin, Derek S, Berry, William AD, Blake, Peter G, Chambers, Laura C, Chan, Patricia CK, Delbrouck, Nicole F, Devereaux, Philip J, Goluch, Richard J, Gregor, Laura H, Grimshaw, Jeremy M, Hanson, Garth J, Illiescu, Eduard A, Jain, Arsh K, Killin, Lauren, Lok, Charmaine E, Luo, Bin, Mustafa, Reem A, Nathoo, Bharat C, Nesrallah, Gihad E, Oliver, Matt J, Pandeya, Sanjay, Parmar, Malvinder S, Perkins, David N, Presseau, Justin, Rabin, Elijah Z, Sasal, Joanna T, Shulman, Tanya S, Smith, D Michael, Sood, Manish, Steele, Andrew W, Tam, Paul YW, Tascona, Daniel J, Wadehra, Davinder B, Wald, Ron, Walsh, Michael, Watson, Paul A, Wodchis, Walter P, Zager, Philip G, Zwarenstein, Merrick, and McIntyre, Christopher W

Published
2022
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2. Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND).

Author

Iyengar, Sudha K, Sedor, John R, Freedman, Barry I, Kao, WH Linda, Kretzler, Matthias, Keller, Benjamin J, Abboud, Hanna E, Adler, Sharon G, Best, Lyle G, Bowden, Donald W, Burlock, Allison, Chen, Yii-Der Ida, Cole, Shelley A, Comeau, Mary E, Curtis, Jeffrey M, Divers, Jasmin, Drechsler, Christiane, Duggirala, Ravi, Elston, Robert C, Guo, Xiuqing, Huang, Huateng, Hoffmann, Michael Marcus, Howard, Barbara V, Ipp, Eli, Kimmel, Paul L, Klag, Michael J, Knowler, William C, Kohn, Orly F, Leak, Tennille S, Leehey, David J, Li, Man, Malhotra, Alka, März, Winfried, Nair, Viji, Nelson, Robert G, Nicholas, Susanne B, O'Brien, Stephen J, Pahl, Madeleine V, Parekh, Rulan S, Pezzolesi, Marcus G, Rasooly, Rebekah S, Rotimi, Charles N, Rotter, Jerome I, Schelling, Jeffrey R, Seldin, Michael F, Shah, Vallabh O, Smiles, Adam M, Smith, Michael W, Taylor, Kent D, Thameem, Farook, Thornley-Brown, Denyse P, Truitt, Barbara J, Wanner, Christoph, Weil, E Jennifer, Winkler, Cheryl A, Zager, Philip G, Igo, Robert P, Hanson, Robert L, Langefeld, Carl D, and Family Investigation of Nephropathy and Diabetes (FIND)

Subjects
Family Investigation of Nephropathy and Diabetes, Humans, Diabetic Nephropathies, Diabetes Mellitus, Type 2, Genetic Predisposition to Disease, RNA-Binding Proteins, African Americans, Indians, North American, European Continental Ancestry Group, Hispanic Americans, United States, Genome-Wide Association Study, Diabetes, Genetics, Human Genome, Clinical Research, Kidney Disease, American Indian or Alaska Native, Prevention, 2.1 Biological and endogenous factors, Metabolic and endocrine, Renal and urogenital, Developmental Biology
Abstract

Diabetic kidney disease (DKD) is the most common etiology of chronic kidney disease (CKD) in the industrialized world and accounts for much of the excess mortality in patients with diabetes mellitus. Approximately 45% of U.S. patients with incident end-stage kidney disease (ESKD) have DKD. Independent of glycemic control, DKD aggregates in families and has higher incidence rates in African, Mexican, and American Indian ancestral groups relative to European populations. The Family Investigation of Nephropathy and Diabetes (FIND) performed a genome-wide association study (GWAS) contrasting 6,197 unrelated individuals with advanced DKD with healthy and diabetic individuals lacking nephropathy of European American, African American, Mexican American, or American Indian ancestry. A large-scale replication and trans-ethnic meta-analysis included 7,539 additional European American, African American and American Indian DKD cases and non-nephropathy controls. Within ethnic group meta-analysis of discovery GWAS and replication set results identified genome-wide significant evidence for association between DKD and rs12523822 on chromosome 6q25.2 in American Indians (P = 5.74x10-9). The strongest signal of association in the trans-ethnic meta-analysis was with a SNP in strong linkage disequilibrium with rs12523822 (rs955333; P = 1.31x10-8), with directionally consistent results across ethnic groups. These 6q25.2 SNPs are located between the SCAF8 and CNKSR3 genes, a region with DKD relevant changes in gene expression and an eQTL with IPCEF1, a gene co-translated with CNKSR3. Several other SNPs demonstrated suggestive evidence of association with DKD, within and across populations. These data identify a novel DKD susceptibility locus with consistent directions of effect across diverse ancestral groups and provide insight into the genetic architecture of DKD.

Published
2015

3. Troponin I and NT-proBNP and the Association of Systolic Blood Pressure With Outcomes in Incident Hemodialysis Patients: The Choices for Healthy Outcomes in Caring for ESRD (CHOICE) Study

Author

Shafi, Tariq, Zager, Philip G, Sozio, Stephen M, Grams, Morgan E, Jaar, Bernard G, Christenson, Robert H, Boulware, L Ebony, Parekh, Rulan S, Powe, Neil R, and Coresh, Josef

Subjects
Biomedical and Clinical Sciences, Clinical Sciences, Bioengineering, Cardiovascular, Prevention, Kidney Disease, Heart Disease, Clinical Research, Good Health and Well Being, Biomarkers, Blood Pressure, Female, Humans, Kidney Failure, Chronic, Male, Middle Aged, Natriuretic Peptide, Brain, Peptide Fragments, Prognosis, Prospective Studies, Renal Dialysis, Troponin I, End-stage renal disease, hypertension, troponin I, N-terminal pro-brain natriuretic peptide, dialysis, epidemiology, hemodialysis, mortality, outcomes, systolic blood pressure, Public Health and Health Services, Urology & Nephrology, Clinical sciences
Abstract

Background: There is uncertainty regarding treatment of hypertension in hemodialysis patients due to the observed J-shaped association between blood pressure (BP) and death. We hypothesized that this association reflects confounding by cardiovascular disease (CVD) and that stratification by CVD biomarkers, cardiac troponin I (cTnI) and N-terminal fragment of prohormone brain natriuretic peptide (NT-proBNP), might change this association. Study Design: National prospective cohort study. Setting & Participants: 446 incident hemodialysis patients. Predictor: Predialysis systolic BP. Outcomes: Mortality (all-cause and CVD) and first CVD event assessed using Cox regression adjusted for demographics, comorbid conditions, and clinical factors. Measurements: Participants with cTnI level ≥ 0.1 ng/mL or NT-proBNP level ≥ 9,252 pg/mL were classified as the high-biomarker group; remaining participants were included in the low-biomarker group. Results: Participants in the high-biomarker group (n = 138 [31%]) were older (61 vs 57 years) and had a higher prevalence of CVD (67% vs 23%), but similar baseline BPs (152 vs 153 mm Hg). There were 323 deaths (143 from CVD) and 271 CVD events. The high-biomarker group had a higher risk of mortality than the low-biomarker group (HR, 1.75; 95% CI, 1.37-2.24). The association between BP and outcomes differed between the 2 biomarker groups (P for interaction = 0.01, 0.2, and 0.07 for all-cause mortality, CVD mortality, and first CVD event, respectively). In the low-biomarker group, BP was associated with greater risk of outcomes: HR per 10 mm Hg higher BP was 1.07 (95% CI, 1.01-1.14), 1.10 (95% CI, 0.96-1.25), and 1.04 (95% CI, 0.96-1.13) for all-cause mortality, CVD mortality, and first CVD event, respectively. Importantly, lower BP was not associated with increased risk of outcomes in stratified models, including for those in high biomarker group. Limitations: BP measurements not standardized. Conclusions: The observed J-shaped association between BP and outcomes in hemodialysis patients is due to confounding by subclinical CVD. A stratification approach based on cTnI and NT-proBNP levels has the potential to inform BP treatment in hemodialysis patients. © 2014 National Kidney Foundation, Inc.

Published
2014

5. A Genome-Wide Search for Linkage of Estimated Glomerular Filtration Rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND)

Author

Thameem, Farook, Igo, Robert P, Freedman, Barry I, Langefeld, Carl, Hanson, Robert L, Schelling, Jeffrey R, Elston, Robert C, Duggirala, Ravindranath, Nicholas, Susanne B, Goddard, Katrina A. B, Divers, Jasmin, Guo, Xiuqing, Ipp, Eli, Kimmel, Paul L, Meoni, Lucy A, Shah, Vallabh O, Smith, Michael W, Winkler, Cheryl A, Zager, Philip G, Knowler, William C, Nelson, Robert G, Pahl, Madeline V, Parekh, Rulan S, Kao, W. H. Linda, Rasooly, Rebekah S, Adler, Sharon G, Abboud, Hanna E, Iyengar, Sudha K, Sedor, John R, and Cai, Tao

Subjects
Chronic Kidney-Disease, Renal-Function, Mexican-Americans, Genetic-Variants, Serum Creatinine, Identifies 6, Association, Loci, Albuminuria, Traits
Published
2013

6. Genomewide linkage scan for diabetic renal failure and albuminuria: the FIND study.

Author

Igo, Robert P, Jr, Iyengar, Sudha K, Nicholas, Susanne B, Goddard, Katrina A B, Langefeld, Carl D, Hanson, Robert L, Duggirala, Ravindranath, Divers, Jasmin, Abboud, Hanna, Adler, Sharon G, Arar, Nedal H, Horvath, Amanda, Elston, Robert C, Bowden, Donald W, Guo, Xiuqing, Ipp, Eli, Kao, W H Linda, Kimmel, Paul L, Knowler, William C, Meoni, Lucy A, Molineros, Julio, Nelson, Robert G, Pahl, Madeline V, Parekh, Rulan S, Rasooly, Rebekah S, Schelling, Jeffrey R, Shah, Vallabh O, Smith, Michael W, Winkler, Cheryl A, Zager, Philip G, Sedor, John R, and Freedman, Barry I

Subjects
Aged, Albuminuria: genetics, metabolism, Chromosome Mapping, Diabetic Nephropathies: genetics, metabolism, Ethnic Groups, Female, Genetic Linkage, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Middle Aged, Pedigree, Polymorphism, Single Nucleotide, Renal Insufficiency: genetics, metabolism, Risk, Time Factors
Abstract

Diabetic nephropathy (DN) is a leading cause of mortality and morbidity in patients with type 1 and type 2 diabetes. The multicenter FIND consortium aims to identify genes for DN and its associated quantitative traits, e.g. the urine albumin:creatinine ratio (ACR). Herein, the results of whole-genome linkage analysis and a sparse association scan for ACR and a dichotomous DN phenotype are reported in diabetic individuals.A genomewide scan comprising more than 5,500 autosomal single nucleotide polymorphism markers (average spacing of 0.6 cM) was performed on 1,235 nuclear and extended pedigrees (3,972 diabetic participants) ascertained for DN from African-American (AA), American-Indian (AI), European-American (EA) and Mexican-American (MA) populations.Strong evidence for linkage to DN was detected on chromosome 6p (p = 8.0 × 10(-5), LOD = 3.09) in EA families as well as suggestive evidence for linkage to chromosome 7p in AI families. Regions on chromosomes 3p in AA, 7q in EA, 16q in AA and 22q in MA displayed suggestive evidence of linkage for urine ACR. The linkage peak on chromosome 22q overlaps the MYH9/APOL1 gene region, previously implicated in AA diabetic and nondiabetic nephropathies.These results strengthen the evidence for previously identified genomic regions and implicate several novel loci potentially involved in the pathogenesis of DN.

Published
2011

9. Antihypertensive medications and risk of death and hospitalizations in US hemodialysis patients: Evidence from a cohort study to inform hypertension treatment practices

Author

Shafi, Tariq, Sozio, Stephen M., Luly, Jason, Bandeen-Roche, Karen J., St. Peter, Wendy L., Ephraim, Patti L., McDermott, Aidan, Herzog, Charles A., Crews, Deidra C., Scialla, Julia J., Tangri, Navdeep, Miskulin, Dana C., Michels, Wieneke M., Jaar, Bernard G., Zager, Philip G., Meyer, Klemens B., Wu, Albert W., and Boulware, L. Ebony

Published
2017
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10. Comparison of Dialysis Unit and Home Blood Pressures: An Observational Cohort Study

Author

Miskulin, Dana C., primary, Jiang, Huan, additional, Gul, Ambreen, additional, Pankratz, V. Shane, additional, Paine, Susan S., additional, Gassman, Jennifer J., additional, Jhamb, Manisha, additional, Kwong, Raymond Y., additional, Negrea, Lavinia, additional, Ploth, David W., additional, Shaffi, Saeed Kamran, additional, Harford, Antonia M., additional, and Zager, Philip G., additional

Published
2021
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15. Coordinated increase in albumin, fibrinogen, and muscle protein synthesis during hemodialysis: role of cytokines

Author

Raj, Dominic S.C., Dominic, Elizabeth A., Wolfe, Robert, Shah, Vallabh O., Bankhurst, Arthur, Zager, Philip G., and Ferrando, Arny

Subjects
Hemodialysis -- Research, Biological sciences
Abstract

Raj, Dominic S. C., Elizabeth A. Dominic, Robert Wolfe, Vanabh O. Shah, Arthur Bankhurst, Philip G. Zager, and Arny Ferrando. Coordinated increase in albumin, fibrinogen, and muscle protein synthesis during hemodialysis: role of cytokines. Am J Physiol Endocrinol Metab 286: E658-E664, 2004. First published January 13, 2004; 10.1152/ajpendo.00444.2003.--Serum albumin, fibrinogen levels, and lean body mass are important predictors of outcome in end-stage renal disease (ESRD). We estimated the fractional synthesis rates of albumin (FSR-A), fibrinogen (FSR-F), and muscle protein (FSR-M) in nine ESRD patients and eight controls, using primed constant infusion of [L-[ring-.sup.13.C.sub.6]]phenylalanine. Cytokine profile and arteriovenous balance of amino acids were also measured. ESRD patients were studied before (Pre-HD) and during hemodialysis (HD). Plasma IL-6, IL-10, and C-reactive protein increased significantly during HD. Despite a decrease in the delivery of amino acids to the leg, the outflow of the amino acids increased during HD. The net balance of amino acids became more negative during HD, indicating release from the muscle. HD increased leg muscle protein synthesis (45%) and catabolism (108%) but decreased whole body proteolysis (15%). FSR-A during HD ([9.7 [+ or -] 0.9%/day) was higher than pre-HD (6.5 [+ or -] 0.9%/day) and controls (5.8 [+ or -] 0.5%/day, P < 0.01). FSR-F increased during HD (19.7 [+ or -] 2.6%/day vs. 11.8 [+ or -] 0.6%/day, P < 0.01), but it was not significantly different from that of controls (14.4 [+ or -] 1.4%/day). FSR-M intradialysis (1.77 [+ or -] 0.19%/day) was higher than pre-HD (1.21 [+ or -] 0.25%/day) and controls (1.30 [+ or -] 0.32%/ day, P < 0.001). Pre-HD FSR-A, FSR-F, and FSR-M values were comparable to those of controls. There was a significant and positive correlation between plasma IL-6 and the FSRs. Thus, in ESRD patients without metabolic acidosis, the fractional synthesis rates of albumin, fibrinogen, and muscle protein are not decreased pre-HD. However, HD increases the synthesis of albumin, fibrinogen, and muscle protein. The coordinated increase in the FSRs is facilitated by constant delivery of amino acids derived from the muscle catabolism and intradialytic increase in IL-6. protein catabolism; protein turnover; inflammation: amino acid; endstage renal disease

Published
2004

20. Genome-Wide Scan for Estimated Glomerular Filtration Rate in Multi-Ethnic Diabetic Populations: The Family Investigation of Nephropathy and Diabetes (FIND)

Author

Schelling, Jeffrey R., Abboud, Hanna E., Nicholas, Susanne B., Pahl, Madeleine V., Sedor, John R., Adler, Sharon G., Arar, Nedal H., Bowden, Donald W., Elston, Robert C., Freedman, Barry I., Goddard, Katrina A.B., Guo, Xiuqing, Hanson, Robert L., Ipp, Eli, Iyengar, Sudha K., Jun, Gyungah, Kao, W. H. Linda, Kasinath, Balakuntalam S., Kimmel, Paul L., Klag, Michael J., Knowler, William C., Nelson, Robert G., Parekh, Rulan S., Quade, Shannon R., Rich, Stephen S., Saad, Mohammed F., Scavini, Marina, Smith, Michael W., Taylor, Kent, Winkler, Cheryl A., Zager, Philip G., and Shah, Vallabh O.

Published
2008

22. Genome-Wide Scans for Diabetic Nephropathy and Albuminuria in Multiethnic Populations: The Family Investigation of Nephropathy and Diabetes (FIND)

Author

Iyengar, Sudha K., Abboud, Hanna E., Goddard, Katrina A.B., Saad, Mohammed F., Adler, Sharon G., Arar, Nedal H., Bowden, Donald W., Duggirala, Ravi, Elston, Robert C., Hanson, Robert L., Ipp, Eli, Kao, W. H. Linda, Kimmel, Paul L., Klag, Michael J., Knowler, William C., Meoni, Lucy A., Nelson, Robert G., Nicholas, Susanne B., Pahl, Madeleine V., Parekh, Rulan S., Quade, Shannon R.E., Rich, Stephen S., Rotter, Jerome I., Scavini, Marina, Schelling, Jeffrey R., Sedor, John R., Sehgal, Ashwini R., Shah, Vallabh O., Smith, Michael W., Taylor, Kent D., Winkler, Cheryl A., Zager, Philip G., and Freedman, Barry I.

Published
2007

25. Kidney disease among the Zuni Indians: The Zuni Kidney Project

Author

SCAVINI, MARINA, SHAH, VALLABH O., STIDLEY, CHRISTINE A., TENTORI, FRANCESCA, PAINE, SUSAN S., HARFORD, ANTONIA M., NARVA, ANDREW S., KESSLER, DAVID S., BOBELU, ARLENE, ALBERT, CARLETON P., BOBELU, JEANETTE, JAMON, EUNICE, NATACHU, KATHY, NEHA, DONICA, WELTY, THOMAS K., MACCLUER, JEAN W., and ZAGER, PHILIP G.

Published
2005

28. Prevalence of Diabetes Is Higher Among Female than Male Zuni Indians

Author

Scavini, Marina, Stidley, Christine A., Shah, Vallabh O., Narva, Andrew S., Tentori, Francesca, Kessler, David S., Bobelu, Arlene, Albert, Carleton P., Bobelu, Jeanette, Jamon, Eunice, Natachu, Kathy, Neha, Donica, Waikaniwa, Mildred, Welty, Thomas K., MacCluer, Jean W., and Zager, Philip G.

Published
2003

36. Satisfaction with Care of Patients on Hemodialysis

Author

Richardson, Michelle M., primary, Paine, Susan S., additional, Grobert, Megan E., additional, Stidley, Christine A., additional, Gabbay, Ezra, additional, Harford, Antonia M., additional, Zager, Philip G., additional, Miskulin, Dana C., additional, and Meyer, Klemens B., additional

Published
2015
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37. Genetics of kidney disease and related cardiometabolic phenotypes in Zuni Indians: the Zuni Kidney Project

Author

Laston, Sandra L., primary, Voruganti, V. Saroja, additional, Haack, Karin, additional, Shah, Vallabh O., additional, Bobelu, Arlene, additional, Bobelu, Jeanette, additional, Ghahate, Donica, additional, Harford, Antonia M., additional, Paine, Susan S., additional, Tentori, Francesca, additional, Cole, Shelley A., additional, MacCluer, Jean W., additional, Comuzzie, Anthony G., additional, and Zager, Philip G., additional

Published
2015
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38. Predialysis Systolic BP Variability and Outcomes in Hemodialysis Patients

Author

Shafi, Tariq, primary, Sozio, Stephen M., additional, Bandeen-Roche, Karen J., additional, Ephraim, Patti L., additional, Luly, Jason R., additional, St. Peter, Wendy L., additional, McDermott, Aidan, additional, Scialla, Julia J., additional, Crews, Deidra C., additional, Tangri, Navdeep, additional, Miskulin, Dana C., additional, Michels, Wieneke M., additional, Jaar, Bernard G., additional, Herzog, Charles A., additional, Zager, Philip G., additional, Meyer, Klemens B., additional, Wu, Albert W., additional, and Boulware, L. Ebony, additional

Published
2014
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40. Heritability of serum sodium concentration: evidence for sex- and ethnic-specific effects

Author

Wilmot, Beth, primary, Voruganti, V. Saroja, additional, Chang, Yen-Pei C., additional, Fu, Yi, additional, Chen, Zhan, additional, Taylor, Herman A., additional, Wilson, James G., additional, Gipson, Teresa, additional, Shah, Vallabh O., additional, Umans, Jason G., additional, Flessner, Michael F., additional, Hitzemann, Robert, additional, Shuldiner, Alan R., additional, Comuzzie, Anthony G., additional, McWeeney, Shannon, additional, Zager, Philip G., additional, MacCluer, Jean W., additional, Cole, Shelley A., additional, and Cohen, David M., additional

Published
2012
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41. Heritability of Measures of Kidney Disease Among Zuni Indians: The Zuni Kidney Project

Author

MacCluer, Jean W., primary, Scavini, Marina, additional, Shah, Vallabh O., additional, Cole, Shelley A., additional, Laston, Sandra L., additional, Voruganti, V. Saroja, additional, Paine, Susan S., additional, Eaton, Alfred J., additional, Comuzzie, Anthony G., additional, Tentori, Francesca, additional, Pathak, Dorothy R., additional, Bobelu, Arlene, additional, Bobelu, Jeanette, additional, Ghahate, Donica, additional, Waikaniwa, Mildred, additional, and Zager, Philip G., additional

Published
2010
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43. Genome‐wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations—significant evidence for linkage on chromosome 4q in African Americans: the Family Investigation of Nephropathy and Diabetes Research Group

Author

Malhotra, Alka, primary, Igo Jr, Robert P., additional, Thameem, Farook, additional, Kao, W. H. Linda, additional, Abboud, Hanna E., additional, Adler, Sharon G., additional, Arar, Nedal H., additional, Bowden, Donald W., additional, Duggirala, Ravindranath, additional, Freedman, Barry I., additional, Goddard, Katrina A. B., additional, Ipp, Eli, additional, Iyengar, Sudha K., additional, Kimmel, Paul L., additional, Knowler, William C., additional, Kohn, Orly, additional, Leehey, David, additional, Meoni, Lucy A., additional, Nelson, Robert G., additional, Nicholas, Susanne B., additional, Parekh, Rulan S., additional, Rich, Stephen S., additional, Chen, Yii‐Der I., additional, Saad, Mohammed F., additional, Scavini, Marina, additional, Schelling, Jeffrey R., additional, Sedor, John R., additional, Shah, Vallabh O., additional, Taylor, Kent D., additional, Thornley‐Brown, Denyse, additional, Zager, Philip G., additional, Horvath, Amanda, additional, and Hanson, Robert L., additional

Published
2009
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46. Heritability of the Severity of Diabetic Retinopathy: The FIND-Eye Study

Author

Arar, Nedal H., primary, Freedman, Barry I., additional, Adler, Sharon G., additional, Iyengar, Sudha K., additional, Chew, Emily Y., additional, Davis, Mathew D., additional, Satko, Scott G., additional, Bowden, Donald W., additional, Duggirala, Ravi, additional, Elston, Robert C., additional, Guo, Xiuxing, additional, Hanson, Robert L., additional, Igo, Robert P., additional, Ipp, Eli, additional, Kimmel, Paul L., additional, Knowler, William C., additional, Molineros, Julio, additional, Nelson, Robert G., additional, Pahl, Madeleine V., additional, Quade, Shannon R. E., additional, Rasooly, Rebekah S., additional, Rotter, Jerome I., additional, Saad, Mohammed F., additional, Scavini, Marina, additional, Schelling, Jeffrey R., additional, Sedor, John R., additional, Shah, Vallabh O., additional, Zager, Philip G., additional, and Abboud, Hanna E., additional

Published
2008
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49. Which Targets in Clinical Practice Guidelines Are Associated with Improved Survival in a Large Dialysis Organization?

Author

Tentori, Francesca, primary, Hunt, William C., additional, Rohrscheib, Mark, additional, Zhu, Min, additional, Stidley, Christine A., additional, Servilla, Karen, additional, Miskulin, Dana, additional, Meyer, Klemens B., additional, Bedrick, Edward J., additional, Johnson, H. Keith, additional, and Zager, Philip G., additional

Published
2007
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50. The Burden of Chronic Kidney Disease among the Zuni Indians

Author

Scavini, Marina, primary, Stidley, Christine A., additional, Paine, Susan S., additional, Shah, Vallabh O., additional, Tentori, Francesca, additional, Bobelu, Arlene, additional, Welty, Thomas K., additional, MacCluer, Jean W., additional, and Zager, Philip G., additional

Published
2007
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