Conventional Phenylketonuria Treatment
作者： Guillén-López Sara , López-Mejía Lizbeth Alejandra , Ibarra-González Isabel , Vela-Amieva Marcela
关键词:
摘要: Phenylketonuria (PKU) is caused by a deficient activity of enzyme phenylalanine (Phe) hydroxylase, which results in high Phe blood concentration, toxic to the central nervous system. The f...
sagepub.com
core.ac.uk
doaj.org参考文章(44)
Horst Bickel, John Gerrard, EvelynM. Hickmans, Influence of phenylalanine intake on phenylketonuria. The Lancet. ,vol. 265, pp. 812- 813 ,(1953) , 10.1016/S0140-6736(53)90473-5
T. Bosdet, J. Branov, C. Selvage, M. Yousefi, S. Sirrs, Diet History Is a Reliable Predictor of Suboptimal Docosahexaenoic Acid Levels in Adult Patients with Phenylketonuria JIMD reports. ,vol. 21, pp. 97- 102 ,(2014) , 10.1007/8904_2014_399
S. Yannicelli, D. M. Medeiros, Elevated plasma phenylalanine concentrations may adversely affect bone status of phenylketonuric mice Journal of Inherited Metabolic Disease. ,vol. 25, pp. 347- 361 ,(2002) , 10.1023/A:1020191515173
G. P.A. Smit, M. van Rijn, T. van Dijk, H. S.A. Heymans, R. Berger, F. J. van Spronsen, D. J. Reijngoud, Plasma phenylalanine and tyrosine responses to different nutritional conditions (fasting/postprandial) in patients with phenylketonuria : effect of sample timing Pediatrics. ,vol. 92, pp. 570- 573 ,(1993)
J R Allen, J C McCauley, D L Waters, J O'Connor, D C Roberts, K J Gaskin, Resting energy expenditure in children with phenylketonuria The American Journal of Clinical Nutrition. ,vol. 62, pp. 797- 801 ,(1995) , 10.1093/AJCN/62.4.797
Vanesa Crujeiras, Luis Aldámiz-Echevarría, Jaime Dalmau, Isidro Vitoria, Fernando Andrade, Iria Roca, Rosaura Leis, Ana Fernandez-Marmiesse, María L. Couce, Vitamin and mineral status in patients with hyperphenylalaninemia Molecular Genetics and Metabolism. ,vol. 115, pp. 145- 150 ,(2015) , 10.1016/J.YMGME.2015.06.010
A. L. Sweeney, R. M. Roberts, J. M. Fletcher, Dietary Protein Counting as an Alternative Way of Maintaining Metabolic Control in Phenylketonuria JIMD reports. ,vol. 3, pp. 131- 139 ,(2012) , 10.1007/8904_2011_31
Judith J. Jans, Monique G.M. de Sain-van der Velden, Peter M. van Hasselt, Dorine T.A.M. van den Hurk, Frederic M. Vaz, Gepke Visser, Nanda M. Verhoeven-Duif, Supplementation with a powdered blend of PUFAs normalizes DHA and AA levels in patients with PKU Molecular Genetics and Metabolism. ,vol. 109, pp. 121- 124 ,(2013) , 10.1016/J.YMGME.2013.03.006
Piotr Adamczyk, Aurelia Morawiec-Knysak, Paweł Płudowski, Beata Banaszak, Jacek Karpe, Wojciech Pluskiewicz, Bone metabolism and the muscle–bone relationship in children, adolescents and young adults with phenylketonuria Journal of Bone and Mineral Metabolism. ,vol. 29, pp. 236- 244 ,(2011) , 10.1007/S00774-010-0216-X
Szimonetta Lohner, Katalin Fekete, Tamás Decsi, Lower n-3 long-chain polyunsaturated fatty acid values in patients with phenylketonuria: a systematic review and meta-analysis. Nutrition Research. ,vol. 33, pp. 513- 520 ,(2013) , 10.1016/J.NUTRES.2013.05.003