MaryZellerStuyMD

Developmental-Behavioral Pediatrics, Medical Genetics

Clinical Assistant Professor of Pediatrics Department of Medical and Molecular Genetics IU School of Medicine

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Indiana University School of MedicineResidency, Pediatrics, 1989 - 1992
University of Texas Health Science Center San Antonio Joe and Teresa Lozano Long School of MedicineResidency, Pediatrics, 1982 - 1985
SUNY Upstate Medical UniversityClass of 1982

PubMed

50 citations
Evidence- and consensus-based recommendations for the use of pegvaliase in adults with phenylketonuria
Nicola Longo, David Dimmock, Harvey L. Levy, Krista Viau, Heather Bausell, Deborah A. Bilder, Barbara K. Burton, Christel Gross, Hope Northrup, Fran Rohr, Stephanie Sa...> ;Genetics in Medicine. 2019 Aug 1
48 citations
Pegvaliase for the treatment of phenylketonuria: A pivotal, double-blind randomized discontinuation Phase 3 clinical trial.
Cary O. Harding, R. Stephen Amato, Mary Stuy, Nicola Longo, Barbara K. Burton, John Posner, Haoling H. Weng, Markus Merilainen, Zhonghua Gu, Joy Jiang, Jerry Vockley, ...> ;Molecular Genetics and Metabolism. 2018 May 1
2 citations
Intermediate MCAD Deficiency Associated with a Novel Mutation of the ACADM Gene: c.1052C>T
Holli M. Drendel, Jason E. Pike, Katherine L. Schumacher, Karen J. Ouyang, Jing Wang, Mary Stuy, Stephen R. Dlouhy, Shaochun Bai> ;Case Reports in Genetics. 2015 Dec 22
31 citations
Mudd’s disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes
Yin-Hsiu Chien, Jose E. Abdenur, Federico Baronio, Allison Anne Bannick, Fernando J. Corrales, María L. Couce, Markus G. Donner, Can Ficicioglu, Cynthia Freehauf, Debo...> ;Orphanet Journal of Rare Diseases. 2015 Aug 20
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