has been cited by the following articles in journals that are participating in CrossRef's forward linking service: |
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| Sapropterin dihydrochloride, 6-R-L-erythro-5,6,7,8-tetrahydrobiopterin, in the treatment of phenylketonuria Kimberlee Michals-Matalon Expert Opinion on Investigational Drugs (2008) 17: 245 Link to Article |
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| Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency Marcel R. Zurflüh, Johannes Zschocke, Martin Lindner, François Feillet, Céline Chery, Alberto Burlina, Raymond C. Stevens, Beat Thöny, and Nenad Blau Human Mutation (2008) 29: 167 Link to Article |
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| Identification of pharmacological chaperones as potential therapeutic agents to treat phenylketonuria Angel L. Pey, Ming Ying, Nunilo Cremades, Adrian Velazquez-Campoy, Tanja Scherer, Beat Thöny, Javier Sancho, and Aurora Martinez Journal of Clinical Investigation (2008) 118: 2858 Link to Article |
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| Genotype–phenotype correlations analysis of mutations in the phenylalanine hydroxylase (PAH) gene Dani Bercovich, Arava Elimelech, Joel Zlotogora, Sigal Korem, Tal Yardeni, Nurit Gal, Nurit Goldstein, Bela Vilensky, Roni Segev, and Smadar Avraham Journal of Human Genetics (2008) 53: 407 Link to Article |
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| What we know that could influence future treatment of phenylketonuria C. N. Sarkissian, A. Gámez, and C. R. Scriver Journal of Inherited Metabolic Disease (2008) Link to Article |
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| Methylmalonic acidaemia: Examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation
group B. Merinero, B. Pérez, C. Pérez-Cerdá, A. Rincón, L. R. Desviat, M. A. Martínez, P. Ruiz Sala, M. J. García, L. Aldamiz-Echevarría, and J. Campos Journal of Inherited Metabolic Disease (2008) 31: 55 Link to Article |
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| Classifying tetrahydrobiopterin responsiveness in the hyperphenylalaninaemias U. Langenbeck Journal of Inherited Metabolic Disease (2008) 31: 67 Link to Article |
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| Mutations in the Regulatory Domain of Phenylalanine Hydroxylase and Response to Tetrahydrobiopterin Lin Wang, Sankar Surendran, Kimberlee Michals-Matalon, Gita Bhatia, Susan Tanskley, Richard Koch, James Grady, Stephen K. Tyring, Raymond C. Stevens, and Flemming Guttler Genetic Testing (2007) 11: 174 Link to Article |
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| ThePAH gene, phenylketonuria, and a paradigm shift Charles R. Scriver Human Mutation (2007) 28: 831 Link to Article |
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| Double blind placebo control trial of large neutral amino acids in treatment of PKU: Effect on blood phenylalanine R. Matalon, M. Giovannini, E. Grechanina, P. Novikov, K. Michals-Matalon, G. Bhatia, A. B. Burlina, A. P. Burlina, C. Braga, and L. Fiori Journal of Inherited Metabolic Disease (2007) 30: 153 Link to Article |
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| Predicted Effects of Missense Mutations on Native-State Stability Account for Phenotypic Outcome in Phenylketonuria, a Paradigm
of Misfolding Diseases A PEY, F STRICHER, L SERRANO, and A MARTINEZ The American Journal of Human Genetics (2007) 81: 1006 Link to Article |
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| B6-responsive disorders: A model of vitamin dependency Peter T. Clayton Journal of Inherited Metabolic Disease (2006) 29: 317 Link to Article |
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| Large neutral amino acids in the treatment of phenylketonuria (PKU) R. Matalon, K. Michals-Matalon, G. Bhatia, E. Grechanina, P. Novikov, J. D. McDonald, J. Grady, S. K. Tyring, and F. Guttler Journal of Inherited Metabolic Disease (2006) 29: 732 Link to Article |
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| Characterization of wild-type and mutant forms of human tryptophan hydroxylase�2 Ingeborg Winge, Jeffrey A. McKinney, Per M. Knappskog, and Jan Haavik Journal of Neurochemistry (2006) 0: 070209222715074 Link to Article |
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