Michelle A. Baum, MD
Co-Director, Kidney Stone Program: Nephrologist, Division of Nephrology
Associate Professor of Pediatrics, Harvard Medical School
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Michelle A. Baum, MD
Co-Director, Kidney Stone Program: Nephrologist, Division of Nephrology
Associate Professor of Pediatrics, Harvard Medical School
Medical Services
Languages
English
Education
Undergraduate School
Northwestern University
1987
Evanston
IL
Medical School
Northwestern University Medical School
1989
Chicago
IL
Internship
Pediatrics
Children's Memorial Hospital
1990
Chicago
IL
Residency
Pediatrics
Children's Memorial Hospital
1992
Chicago
IL
Fellowship
Pediatric Nephrology
Boston Children's Hospital
1996
Boston
MA
Certifications
American Board of Pediatrics (Nephrology)
Therapeutic Pharmaceutical Agents (TPA)
Publications
Understanding Rare Kidney Stone Diseases: A Review. View Abstract
Trio exome sequencing in individuals with CAKUT identifies de novo variants in potential novel candidate genes in 19.62. View Abstract
Global access to management of primary hyperoxaluria: a survey on behalf of OxalEurope, G&K working group of the ERA, and ESPN. View Abstract
Diagnostic Odyssey in a Child with Red-Colored Urine and Proteinuria. View Abstract
Diagnostic Test Characteristics of Ultrasound-Based Hydronephrosis for Chronic Kidney Disease in Children and Adolescents With Myelomeningocele: Results From the UMPIRE and National Spina Bifida Patient Registry Cohort Studies. View Abstract
The role of double heterozygotes of SLC3A1 and SLC7A9 in the prevalence of cystine stones. View Abstract
The evolving landscape of monogenic nephrolithiasis and therapeutic innovations. View Abstract
Opportunities in Primary and Enteric Hyperoxaluria at the Cross-Roads Between the Clinic and Laboratory. View Abstract
Diagnosis and management of primary hyperoxalurias: best practices. View Abstract
OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis. View Abstract
PHYOX2: a pivotal randomized study of nedosiran in primary hyperoxaluria type 1 or 2. View Abstract
Treatment of primary hyperoxaluria type 1. View Abstract
Dietary Risk Factors for Pediatric Kidney Stones: A Case-Control Study. View Abstract
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models. View Abstract
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT. View Abstract
Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease. View Abstract
Safety, pharmacodynamics, and exposure-response modeling results from a first-in-human phase 1 study of nedosiran (PHYOX1) in primary hyperoxaluria. View Abstract
Urodynamic characteristics of neurogenic bladder in newborns with myelomeningocele and refinement of the definition of bladder hostility: Findings from the UMPIRE multi-center study. View Abstract
Incidence of Urinary Tract Infections in Newborns with Spina Bifida-Is Antibiotic Prophylaxis Necessary? View Abstract
Pathophysiology and Treatment of Enteric Hyperoxaluria. View Abstract
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. View Abstract
Pharmacological Dilutional Therapy Using the Vasopressin Antagonist Tolvaptan for Young Patients With Cystinuria: A Pilot Investigation. View Abstract
Evaluation and Medical Management of Patients with Cystine Nephrolithiasis: A Consensus Statement. View Abstract
Kidney Function Surveillance in the National Spina Bifida Patient Registry: A Retrospective Cohort Study. View Abstract
Urologic guidelines for the care and management of people with spina bifida. View Abstract
Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis. View Abstract
Baseline Urinary Tract Imaging in Infants Enrolled in the UMPIRE Protocol for Children with Spina Bifida. View Abstract
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients. View Abstract
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. View Abstract
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ˜43% of 35 Families With Midaortic Syndrome. View Abstract
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome. View Abstract
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. View Abstract
Suppression of microRNA Activity in Kidney Collecting Ducts Induces Partial Loss of Epithelial Phenotype and Renal Fibrosis. View Abstract
Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center. View Abstract
Imaging in the diagnosis of pediatric urolithiasis. View Abstract
Design and Methodological Considerations of the Centers for Disease Control and Prevention Urologic and Renal Protocol for the Newborn and Young Child with Spina Bifida. View Abstract
Mutations in SLC26A1 Cause Nephrolithiasis. View Abstract
Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or Nephrocalcinosis. View Abstract
Imaging and surgical utilization for pediatric cystinuria patients: A single-institution cohort study. View Abstract
Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis. View Abstract
Characteristics and survival of patients with end stage renal disease and spina bifida in the United States renal data system. View Abstract
Continuous renal replacement therapy for children =10 kg: a report from the prospective pediatric continuous renal replacement therapy registry. View Abstract
Nonrenal indications for continuous renal replacement therapy: A report from the Prospective Pediatric Continuous Renal Replacement Therapy Registry Group. View Abstract
Prenatal programming of rat cortical collecting tubule sodium transport. View Abstract
Nucleotide sequence of the Na+/H+ exchanger-8 in patients with congenital sodium diarrhea. View Abstract
Fluid overload and mortality in children receiving continuous renal replacement therapy: the prospective pediatric continuous renal replacement therapy registry. View Abstract
Protein and calorie prescription for children and young adults receiving continuous renal replacement therapy: a report from the Prospective Pediatric Continuous Renal Replacement Therapy Registry Group. View Abstract
Continuous renal replacement therapy (CRRT) after stem cell transplantation. A report from the prospective pediatric CRRT Registry Group. View Abstract
Demographic characteristics of pediatric continuous renal replacement therapy: a report of the prospective pediatric continuous renal replacement therapy registry. View Abstract
Outcome of renal transplantation for Wilms' tumor and Denys-Drash syndrome: a report of the North American Pediatric Renal Transplant Cooperative Study. View Abstract
Multi-centre evaluation of anticoagulation in patients receiving continuous renal replacement therapy (CRRT). View Abstract
Pediatric patients with multi-organ dysfunction syndrome receiving continuous renal replacement therapy. View Abstract
Outcomes after renal transplantation for FSGS in children. View Abstract
Localization of Mg2+-sensing shark kidney calcium receptor SKCaR in kidney of spiny dogfish, Squalus acanthias. View Abstract
Calpain-mediated AQP2 proteolysis in inner medullary collecting duct. View Abstract
Outcome of renal transplantation in adolescents with focal segmental glomerulosclerosis. View Abstract
AQP2 is a substrate for endogenous PP2B activity within an inner medullary AKAP-signaling complex. View Abstract
Loss of living donor renal allograft survival advantage in children with focal segmental glomerulosclerosis. View Abstract
The role of the graft endothelium in transplant rejection: evidence that endothelial activation may serve as a clinical marker for the development of chronic rejection. View Abstract
Recent insights into the coordinate regulation of body water and divalent mineral ion metabolism. View Abstract
The perinatal expression of aquaporin-2 and aquaporin-3 in developing kidney. View Abstract
Vasopressin-elicited water and urea permeabilities are altered in IMCD in hypercalcemic rats. View Abstract
Renovascular hypertension in Marfan syndrome. View Abstract
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