George A Diaz

ORCID

Publication Activity (10 Years)

Years Active: 2014-2022
Publications (10 Years): 11

Top Venues

Orphanet journal of rare diseases

Genetics in medicine : official journal of the American College of Medical Genetics

Journal of inherited metabolic disease

Journal of medical economics

This page only lists publications with an associated author ORCID identifier.

Publications

George A Diaz, Roberto Giugliani, Nathalie Guffon, Simon A Jones, Eugen Mengel, Maurizio Scarpa, Peter Witters, Abhimanyu Yarramaneni, Jing Li, Nicole M Armstrong, Yong Kim, Catherine Ortemann-Renon, Monica Kumar
Long-term safety and clinical outcomes of olipudase alfa enzyme replacement therapy in pediatric patients with acid sphingomyelinase deficiency: two-year results. Orphanet journal of rare diseases 17 (1) (2022)
George A Diaz, Joslyn Crowe, Justin Hopkin
Health insurance literacy and health services access barriers in Niemann-Pick disease: the patient and caregiver voice. Orphanet journal of rare diseases 17 (1) (2022)
George A Diaz, Roberto Giugliani, Nathalie Guffon, Simon A Jones, Eugen Mengel, Maurizio Scarpa, Peter Witters, Abhimanyu Yarramaneni, Jing Li, Nicole M Armstrong, Yong Kim, Catherine Ortemann-Renon, Monica Kumar
Long-term safety and clinical outcomes of olipudase alfa enzyme replacement therapy in pediatric patients with acid sphingomyelinase deficiency: two-year results. Orphanet journal of rare diseases 17 (1) (2022)
George A Diaz, Roberto Giugliani, Nathalie Guffon, Simon A Jones, Eugen Mengel, Maurizio Scarpa, Peter Witters, Abhimanyu Yarramaneni, Jing Li, Nicole M Armstrong, Yong Kim, Catherine Ortemann-Renon, Monica Kumar
Long-term safety and clinical outcomes of olipudase alfa enzyme replacement therapy in pediatric patients with acid sphingomyelinase deficiency: two-year results. Orphanet journal of rare diseases 17 (1) (2022)
George A Diaz, Roberto Giugliani, Nathalie Guffon, Simon A Jones, Eugen Mengel, Maurizio Scarpa, Peter Witters, Abhimanyu Yarramaneni, Jing Li, Nicole M Armstrong, Yong Kim, Catherine Ortemann-Renon, Monica Kumar
Long-term safety and clinical outcomes of olipudase alfa enzyme replacement therapy in pediatric patients with acid sphingomyelinase deficiency: two-year results. Orphanet journal of rare diseases 17 (1) (2022)
George A Diaz, Roberto Giugliani, Nathalie Guffon, Simon A Jones, Eugen Mengel, Maurizio Scarpa, Peter Witters, Abhimanyu Yarramaneni, Jing Li, Nicole M Armstrong, Yong Kim, Catherine Ortemann-Renon, Monica Kumar
Long-term safety and clinical outcomes of olipudase alfa enzyme replacement therapy in pediatric patients with acid sphingomyelinase deficiency: two-year results. Orphanet journal of rare diseases 17 (1) (2022)
Aseel Bin Sawad, John Jackimiec, Mark Bechter, Michael Hull, Jason Yeaw, Yi Wang, George A Diaz
Health care resource utilization in the management of patients with Arginase 1 Deficiency in the US: a retrospective, observational, claims database study. Journal of medical economics 25 (1) (2022)
George A Diaz, Roberto Giugliani, Nathalie Guffon, Simon A Jones, Eugen Mengel, Maurizio Scarpa, Peter Witters, Abhimanyu Yarramaneni, Jing Li, Nicole M Armstrong, Yong Kim, Catherine Ortemann-Renon, Monica Kumar
Long-term safety and clinical outcomes of olipudase alfa enzyme replacement therapy in pediatric patients with acid sphingomyelinase deficiency: two-year results. Orphanet journal of rare diseases 17 (1) (2022)
George A Diaz, Simon A Jones, Maurizio Scarpa, Karl Eugen Mengel, Roberto Giugliani, Nathalie Guffon, Isabela Batsu, Patricia A Fraser, Jing Li, Qi Zhang, Catherine Ortemann-Renon
One-year results of a clinical trial of olipudase alfa enzyme replacement therapy in pediatric patients with acid sphingomyelinase deficiency. Genetics in medicine : official journal of the American College of Medical Genetics 23 (8) (2021)
George A Diaz, Andreas Schulze, Markey C McNutt, Elisa Leão-Teles, J Lawrence Merritt, Gregory M Enns, Spyros Batzios, Allison Bannick, Roberto T Zori, Leslie S Sloan, Susan L Potts, Gillian Bubb, Anthony G Quinn
Clinical effect and safety profile of pegzilarginase in patients with arginase 1 deficiency. Journal of inherited metabolic disease 44 (4) (2021)
Saskia C Sanderson, Michael D Linderman, Randi Zinberg, Ali Bashir, Andrew Kasarskis, Micol Zweig, Sabrina Suckiel, Hardik Shah, Milind Mahajan, George A Diaz, Eric E Schadt
How do students react to analyzing their own genomes in a whole-genome sequencing course?: outcomes of a longitudinal cohort study. Genetics in medicine : official journal of the American College of Medical Genetics 17 (11) (2015)
Brendan Lee, George A Diaz, William Rhead, Uta Lichter-Konecki, Annette Feigenbaum, Susan A Berry, Cindy Le Mons, James A Bartley, Nicola Longo, Sandesh C Nagamani, William Berquist, Renata Gallagher, Dennis Bartholomew, Cary O Harding, Mark S Korson, Shawn E McCandless, Wendy E Smith, Stephen Cederbaum, Derek Wong, J Lawrence Merritt, Andreas Schulze, Jerry Vockley, Gerard Vockley, David Kronn, Roberto Zori, Marshall L Summar, Douglas A Milikien, Miguel Marino, Dion F Coakley, Masoud Mokhtarani, null null, Bruce F Scharschmidt
Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorder. Genetics in medicine : official journal of the American College of Medical Genetics 17 (7) (2014)

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Publication Activity (10 Years)

Top Topics

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George A Diaz