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Biologics: Targets and Therapy Volume 4, 2010 - Issue

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New era in treatment for phenylketonuria: Pharmacologic therapy with sapropterin dihydrochloride

Cary O HardingDepartments of Molecular and Medical Genetics and Pediatrics, Oregon Health & Science University, Portland, Oregon, USACorrespondence[email protected]

Pages 231-236 | Published online: 06 Aug 2010

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Articles from other publishers (7)

María Conde-Giménez, Juan José Galano-Frutos, María Galiana-Cameo, Alejandro Mahía, Bruno L. Victor, Sandra Salillas, Adrián Velázquez-Campoy, Rui M. M. Brito, José Antonio Gálvez, María D. Díaz-de-Villegas & Javier Sancho. (2022) Alchemical Design of Pharmacological Chaperones with Higher Affinity for Phenylalanine Hydroxylase. International Journal of Molecular Sciences 23:9, pages 4502.
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María Conde-Giménez & Javier Sancho. (2021) Unravelling the Complex Denaturant and Thermal-Induced Unfolding Equilibria of Human Phenylalanine Hydroxylase. International Journal of Molecular Sciences 22:12, pages 6539.
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Tracy B. Lowe, Jane DeLuca & Georgianne Arnold. (2020) Neurocognitive, neuropsychiatric, and neurological outcomes associated with phenylalanine hydroxylase deficiency: Assessment considerations for nurse practitioners. Journal for Specialists in Pediatric Nursing 26:1.
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Alireza Azaripour & Hajar Abbasi. (2019) Effect of type and amount of modified corn starches on qualitative properties of low‐protein biscuits for phenylketonuria. Food Science & Nutrition 8:1, pages 281-290.
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Kathryn E. Coakley, Teresa D. Douglas, Michael Goodman, Usha Ramakrishnan, Steven F. Dobrowolski & Rani H. Singh. (2016) Modeling correlates of low bone mineral density in patients with phenylalanine hydroxylase deficiency. Journal of Inherited Metabolic Disease 39:3, pages 363-372.
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J. Belik, A. Weinmann & S. Unger. 2013. Handbook of dietary and nutritional aspects of human breast milk. Handbook of dietary and nutritional aspects of human breast milk 501 514 .

Cary O. Harding & Nenad Blau. (2010) Advances and challenges in phenylketonuria. Journal of Inherited Metabolic Disease 33:6, pages 645-648.
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