Dr. Muenzer is on Doximity
As a Doximity member you'll join over two million verified healthcare professionals in a private, secure network.
- Gain access to free telehealth tools, such as our “call shielding” and one-way patient texting.
- Connect with colleagues in the same hospital or clinic.
- Read the latest clinical news, personalized to your specialty.
Office
101 Manning Dr
Chapel Hill, NC 27514Phone+1 919-966-4131
Education & Training
- National Institutes of Health Clinical Center/Eunice Kennedy Shriver NICHDFellowship, Pediatric Endocrinology, 1982 - 1985
- University of Wisconsin Hospitals and ClinicsResidency, Pediatrics, 1979 - 1982
- Case Western Reserve University School of MedicineClass of 1979
Certifications & Licensure
- NC State Medical License 1993 - 2025
- MI State Medical License 1986 - 2002
- WI State Medical License 1980 - 1999
- MD State Medical License 1983 - 1985
- American Board of Medical Genetics and Genomics Clinical Biochemical/Molecular Genetics
- American Board of Pediatrics Pediatrics
Clinical Trials
- Extension of Study TKT024 Evaluating Long-Term Safety and Clinical Outcomes in MPS II Patients Receiving Idursulfase Start of enrollment: 2004 Sep 13
- A Safety and Dose Ranging Study of Idursulfase (Intrathecal) Administration Via an Intrathecal Drug Delivery Device in Pediatric Patients With Hunter Syndrome Who Have Central Nervous System Involvement and Are Receiving Treatment With Elaprase® Start of enrollment: 2009 Nov 18
- Screening Study to Identify Pediatric Patients With Hunter Syndrome Who Demonstrate Evidence of Central Nervous System (CNS) Involvement and Who Are Currently Receiving Treatment With Elaprase® Start of enrollment: 2009 Jul 02
- Join now to see all
Publications & Presentations
PubMed
- Genotype-phenotype findings in patients with mucopolysaccharidosis II from the Hunter Outcome Survey.Joseph Muenzer, Hernan Amartino, Barbara K Burton, Maurizio Scarpa, Anna Tylki-Szymańska
Molecular Genetics and Metabolism. 2024-09-10 - Evaluation of early treatment with intravenous idursulfase and intrathecal idursulfase-IT on cognitive function in siblings with neuronopathic mucopolysaccharidosis II.Joseph Muenzer, Barbara K Burton, Paul Harmatz, Luis González Gutiérrez-Solana, Matilde Ruiz-Garcia
Journal of Inherited Metabolic Disease. 2024-09-09 - Community consensus for Heparan sulfate as a biomarker to support accelerated approval in Neuronopathic Mucopolysaccharidoses.Joseph Muenzer, Carole Ho, Heather Lau, Mark Dant, Maria Fuller
Molecular Genetics and Metabolism. 2024-08-01
Press Mentions
- Family of NC 5-Year-Old with Rare Disease Searching for Hope After Drug Trial EndsMay 11th, 2021
- Applied Therapeutics to Host Virtual Rare Disease ForumMarch 16th, 2021
- Sangamo Shares Plunge After Interim Results for MPS Candidates Fall Short of Clinical BenefitFebruary 8th, 2019
- Join now to see all
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence: