Wacharee Seeherunvong

ORCID: 0000-0003-0485-5762
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About
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Research Areas
  • Parathyroid Disorders and Treatments
  • Dialysis and Renal Disease Management
  • Renal Diseases and Glomerulopathies
  • Chronic Kidney Disease and Diabetes
  • Pediatric Urology and Nephrology Studies
  • Renal Transplantation Outcomes and Treatments
  • Systemic Lupus Erythematosus Research
  • Renal and related cancers
  • Pharmacological Effects and Toxicity Studies
  • Birth, Development, and Health
  • Hemoglobinopathies and Related Disorders
  • Vitamin D Research Studies
  • Blood Pressure and Hypertension Studies
  • Magnesium in Health and Disease
  • Liver Diseases and Immunity
  • Pregnancy and Medication Impact
  • Acute Kidney Injury Research
  • Genetic Syndromes and Imprinting
  • Hepatitis Viruses Studies and Epidemiology
  • Polyomavirus and related diseases
  • Diabetes and associated disorders
  • Neonatal Health and Biochemistry
  • Complementary and Alternative Medicine Studies
  • Hemodynamic Monitoring and Therapy
  • Iron Metabolism and Disorders

University of Miami
2014-2025

Miami Transplant Institute
2024-2025

Clinical Pharmacology of Miami
2024

University of Miami Hospital
2009-2024

Jackson Memorial Hospital
2001-2023

Jackson Health System
2013-2019

Memorial Medical Center
2012

Pediatric Nephrology of Alabama
2011

Anhui Provincial Children's Hospital
2010

Ramathibodi Hospital
2006

Rituximab (RTX), an anti-CD20 monoclonal antibody, has been proposed for use in the therapy of systemic lupus erythematosus (SLE). We present initial long-term experience safety and efficacy rituximab treatment SLE children. Eighteen patients (mean age 14 ± 3 years) with severe were treated after demonstrating resistance or toxicity to conventional regimens. There was a predominance female (16/18) ethnic African (13/18) patients. All had nephritis [World Health Organization (WHO) classes...

10.1007/s00467-007-0694-9 article EN cc-by-nc Pediatric Nephrology 2007-12-18

Childhood-onset lupus nephritis (LN) carries a worse renal prognosis compared with adults. Controlled treatment trials in children are lacking. We and patient survival cohort of pediatric patients followed over 3 decades.

10.2215/cjn.00910111 article EN Clinical Journal of the American Society of Nephrology 2011-07-29

Vitamin D attenuates uremic cardiac hypertrophy, possibly by suppressing the myocardial renin–angiotensin system (RAS) and fibroblast growth factors (FGFs). We compared suppression of hypertrophy expression RAS FGF receptor genes offered vitamin analog paricalcitol (Pc) or angiotensin-converting enzyme inhibitor enalapril (E) in experimental uremia. Rats with 5/6 nephrectomy received Pc E for 8 weeks. Renal function, systolic blood pressure, were evaluated. Myocardial genes, brain...

10.1093/ajh/hpt177 article EN American Journal of Hypertension 2013-09-26

Abstract Background Primary FSGS manifests with nephrotic syndrome and may recur following KT. Failure to respond conventional therapy after recurrence results in poor outcomes. Evaluation of podocyte B7-1 expression treatment abatacept (a antagonist) has shown promise but remains controversial. Methods From 2012 2020, twelve patients developed post-KT range proteinuria, failed therapy, were treated abatacept. Nine/twelve (< 21 years old) experienced recurrent FSGS; three adults de novo...

10.1007/s00467-022-05549-7 article EN cc-by Pediatric Nephrology 2022-05-04

Long-term survival of kidney allografts is limited by multiple factors, including nonadherence. High intrapatient variability in tacrolimus levels (≥30%) associated with de novo donor-specific antibody (dnDSA) formation, increased risk rejection and graft loss. We prospectively analyzed the association between nonadherence pediatric transplant recipients. derived a composite adherence score from 0 to 3 points based on (1) Basel Assessment Adherence Immunosuppressive Medical Scale©; (2)...

10.3389/frtra.2025.1572928 article EN cc-by Frontiers in Transplantation 2025-03-17

Recent advances in the early diagnosis of fetal CAKUT with an increase surgical interventions have led to a growing number neonatal survivors born severe renal dysfunction. This, turn, has required development multi-disciplinary treatment paradigms individualized management these infants advanced stage kidney disease from birth. Early multi-modal includes directed towards establishing adequate urine flow, respiratory support assessment pulmonary hypoplasia, and metabolic control avoid need...

10.3389/fped.2019.00182 article EN cc-by Frontiers in Pediatrics 2019-05-14
Louis-Philippe Laurin Margaret E. Helmuth Salem Almaani Isabelle Ayoub Dhruti P. Chen and 95 more Leonela Villegas Cynthia C. Nast Bruce Robinson Vimal K. Derebail Meryl Waldman Andrew S. Bomback Wooin Ahn Gerald B. Appel Paul S. Appelbaum Revekka Babayev Andrew S. Bomback Pietro A. Canetta Brenda Chan Vivette D. D’Agati Samitri Dogra Hilda Fernández Ali G. Gharavi William H. Hines S. Ali Husain Namrata G. Jain Krzysztof Kiryluk Fangming Lin Maddalena Marasà Glen S. Markowitz Hila Milo Rasouly Sumit Mohan Nicola Mongera Jordan G. Nestor Thomas L. Nickolas Jai Radhakrishnan Maya K. Rao Simone Sanna‐Cherchi Shayan Shirazian Michael B. Stokes Natalie Uy Anthony M. Valeri Natalie Vena Bartosz Foroncewicz Barbara Moszczuk Krzysztof Mucha Agnieszka Perkowska‐Ptasińska Gian Marco Ghiggeri Francesca Lugani Josephine M. Ambruzs Helen Liapis Rossana Baracco Amrish Jain Isa Ashoor Diego Avilés Tarak Srivastava Sun-Young Ahn Prasad Devarajan Elif Erkan Donna Claes Hillarey Stone Sherene Mason Rasheed Gbadegesin Liliana Gomez-Mendez Larry A. Greenbaum Chia-shi Wang Hong Yin Yi Cai Goebel Jens Julia Steinke Donald J. Weaver Jerome C. Lane Carl H. Cramer Cindy Pan Neil J. Paloian Rajasree Sreedharan David T. Selewski Katherine Twombley Corinna Bowers Mary Dreher Mahmoud Kallash John D. Mahan Samantha Sharpe William E. Smoyer Amira Al‐Uzri Sandra Iragorri Myda Khalid Craig W. Belsha Joseph L. Alge Michael Braun Angela C. Gomez Scott E. Wenderfer Tetyana L. Vasylyeva Daniel I. Feig Gabriel Cara‐Fuentes Melisha Hannah Carla Nester Aftab S. Chishti Jon B. Klein Chryso Katsoufis Wacharee Seeherunvong

10.1016/j.ekir.2025.03.027 article EN cc-by-nc-nd Kidney International Reports 2025-03-01

BackgroundPediatric patients with chronic kidney disease (CKD) are at increased risk of early cardiovascular and premature death. Abnormalities in microvascular structure function may presage end-organ damage including vascular calcification myocardial ischemia associated disordered mineral metabolism. Early detection rarefaction (reduced density capillaries) identify at-risk prompt timely therapeutic interventions. Our objective was to study capillary pediatric hemodialysis (HD) determine...

10.1093/ckj/sfu106 article EN cc-by-nc Clinical Kidney Journal 2014-10-20

In uremic animals, vitamin D receptor (VDR) agonists like paricalcitol (Pc) attenuate cardiac hypertrophy, but this effect has not been replicated consistently in humans with chronic kidney disease. Elevated fibroblast growth factor 23 (FGF23) levels cause hypertrophy activation of the myocardial calcineurin/nuclear activated T cell (NFAT) axis and may antagonize cardioprotective effects VDR agonist therapy. We hypothesized that effectiveness Pc depend on prevailing circulating FGF23 could...

10.1093/ajh/hpy154 article EN American Journal of Hypertension 2018-10-13
Chia-shi Wang Dorey A. Glenn Margaret E. Helmuth Abigail R. Smith Andrew S. Bomback and 95 more Pietro A. Canetta Gaia Coppock Myda Khalid Katherine R. Tuttle Raed Bou-Matar Larry A. Greenbaum Bruce Robinson Lawrence B. Holzman William E. Smoyer Michelle N. Rheault Debbie S. Gipson Laura Mariani Wooin Ahn Gerald B. Appel Paul S. Appelbaum Revekka Babayev Brenda Chan Vivette D. D’Agati Samitri Dogra Hilda Fernández Ali G. Gharavi William H. Hines S. Ali Husain Namrata G. Jain Krzysztof Kiryluk Fangming Lin Maddalena Marasà Glen S. Markowitz Hila Milo Rasouly Sumit Mohan Nicola Mongera Jordan G. Nestor Thomas L. Nickolas Jai Radhakrishnan Maya K. Rao Simone Sanna‐Cherchi Shayan Shirazian Michael B. Stokes Natalie Uy Anthony M. Valeri Natalie Vena Bartosz Foroncewicz Barbara Moszczuk Krzysztof Mucha Agnieszka Perkowska‐Ptasińska Gian Marco Ghiggeri Francesca Lugani Josephine M. Ambruzs Helen Liapis Rossana Baracco Amrish Jain Isa Ashoor Diego Avilés Tarak Srivastava Sun-Young Ahn Prasad Devarajan Elif Erkan Donna Claes Hillarey Stone Sherene Mason Rasheed Gbadegesin Liliana Gomez-Mendez Hong Yin Yi Cai Goebel Jens Julia Steinke Donald J. Weaver Jerome C. Lane Carl H. Cramer Cindy Pan Neil J. Paloian Rajasree Sreedharan David T. Selewski Katherine Twombley Corinna Bowers Mary Dreher Mahmoud Kallash John D. Mahan Samantha Sharpe Amira Al‐Uzri Sandra Iragorri Craig W. Belsha Joseph L. Alge Michael Braun Angela C. Gomez Scott E. Wenderfer Tetyana L. Vasylyeva Daniel I. Feig Gabriel Cara‐Fuentes Melisha Hannah Carla Nester Aftab S. Chishti Jon B. Klein Chryso Katsoufis Wacharee Seeherunvong

10.1053/j.ajkd.2023.07.008 article EN publisher-specific-oa American Journal of Kidney Diseases 2023-08-31

Background Mutations of the Wilms tumor suppressor-1 gene ( WT1) are associated with life-threatening glomerulopathy, disorders sexual development, Wilm's tumor, and gonadal malignancies. Our objectives were to describe clinical presentations, age progression, onset complications WT1 mutation through a case series literature review. Methods A retrospective study included all patients followed at University Miami/Holtz Children's Hospital from January 2000 December 2020 diagnosis . review...

10.3389/fped.2022.847295 article EN cc-by Frontiers in Pediatrics 2022-04-15

10.1016/j.kint.2023.06.020 article EN publisher-specific-oa Kidney International 2023-06-29

Background The mechanisms responsible for the hyperphosphatemia in patients with sickle cell disease (SCD) and preserved glomerular filtration rate (GFR) are not fully understood. role of fibroblast growth factor 23 (FGF23), a phosphaturic hormone has been investigated SCD. Hence, we evaluated parameters renal tubular phosphorus handling their relation to prevailing FGF23 levels cohort young SCD patients. Methods Renal phosphate circulating various analytes including parathyroid (PTH) were...

10.1002/pbc.25188 article EN Pediatric Blood & Cancer 2014-08-17
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