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Original Article

Effect of experimental hyperphenylalaninemia on myelin metabolism at later stages of brain development

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Pages 217-227 | Received 06 Jan 1983, Published online: 07 Jul 2009

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Lili Liang, Xuefan Gu, Duan Li & Lihua Lu. (2011) The Expression and Phosphorylation of Acid Sensing Ion Channel 1a in the Brain of a Mouse Model of Phenylketonuria. International Journal of Neuroscience 121:7, pages 399-404.
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Articles from other publishers (21)

Valentina Rovelli & Nicola Longo. (2023) Phenylketonuria and the brain. Molecular Genetics and Metabolism 139:1, pages 107583.
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Mariana B. M. de Moraes, Hygor M. R. de Souza, Maria L. C. de Oliveira, Roy W. A. Peake, Fernanda B. Scalco & Rafael Garrett. (2023) Combined targeted and untargeted high-resolution mass spectrometry analyses to investigate metabolic alterations in pompe disease. Metabolomics 19:4.
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Alina A. Ushakova, Helena A. Gubkina, Victoria A. Kachur & Eugene A. Lepekhin. (1998) Effect of experimental hyperphenylalaninemia on the postnatal rat brain. International Journal of Developmental Neuroscience 15:1, pages 29-36.
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J H Walter. (1995) Late effects of phenylketonuria.. Archives of Disease in Childhood 73:6, pages 485-486.
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Maureen A. Cleary, John H. Walter, James E. Wraith, Fiona White, Kathryn Tyler & Jeremy P.R. Jenkins. (1995) Magnetic resonance imaging in phenylketonuria: Reversal of cerebral white matter change. The Journal of Pediatrics 127:2, pages 251-255.
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FA Hommes. (1994) Loss of neurotransmitter receptors by hyperphenylalaninemia in the HPH-5 mouse brain. Acta Paediatrica 83:s407, pages 120-121.
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M.A Cleary, J.H Walter, J.E Wraith, S.M Alani, D Whittle, J.P.R Jenkins & K Tyler. (1994) Magnetic resonance imaging of the brain in phenylketonuria. The Lancet 344:8915, pages 87-90.
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U. Bick, K. Ullrich, U. Stöber, H. Möller, G. Schuierer, A. C. Ludolph, C. Oberwittler, J. Weglage & U. Wendel. (1993) White matter abnormalities in patients with treated hyperphenylalaninaemia: Magnetic resonance relaxometry and proton spectroscopy findings. European Journal of Pediatrics 152:12, pages 1012-1020.
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F. A. Hommes. (1993) The effect of hyperphenylalaninaemia on the muscarinic acetylcholine receptor in the HPH‐5 mouse brain. Journal of Inherited Metabolic Disease 16:6, pages 962-974.
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F. A. Hommes & L. Moss. (1991) Myelin turnover in hyperphenylalaninaemia. A re‐evaluation with the HPH‐5 mouse. Journal of Inherited Metabolic Disease 15:2, pages 243-251.
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Frits A. Hommes. (1991) On the mechanism of permanent brain dysfunction in hyperphenylalaninemia. Biochemical Medicine and Metabolic Biology 46:3, pages 277-287.
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FRITS A. HOMMES. (1990) Demyelination in Hyperphenylalaninemia. Annals of the New York Academy of Sciences 605:1 Myelination a, pages 449-452.
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F. A. Hommes. (1988) The role of the blood‐brain barrier in the aetiology of permanent brain dysfunction in hyperphenylalaninaemia. Journal of Inherited Metabolic Disease 12:1, pages 41-46.
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Kiyosato Matsuo & Frits A. Hommes. (1988) The development of the muscarinic acetylcholine receptor in normal and hyperphenylalaninemic rat cerebrum. Neurochemical Research 13:9, pages 867-870.
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Frits A. Hommes & Kiyosato Matsuo. 1988. Dietary Phenylalanine and Brain Function. Dietary Phenylalanine and Brain Function 238 243 .
K. Matsuo, L. Moss & F. A. Hommes. (1987) Properties of the 3?-phosphoadenosine-5?-phosphosulfate (PAPS) synthesizing systems of brain and liver. Neurochemical Research 12:4, pages 345-349.
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K. Matsuo & F. Hommes. (1986) Regional distribution of the phenylalanine‐sensitive ATP‐sulphurylase in brain. Journal of Inherited Metabolic Disease 10:1, pages 62-65.
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J. Schröter, K. ‐J. Schott, M. ‐A. Purtill & V. Neuhoff. (1986) Lysosomal protein degradation in experimental hyperphenylalaninaemia. Journal of Inherited Metabolic Disease 9:3, pages 273-282.
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Shusuke Hirano, Yoshio Takagi, Tomoyuki Kanamatsu & Kenji Nakai. (1985) Effects of hyperphenylalaninemia in the fetal stage on the postnatal development of fetal rat brain. Neurochemical Research 10:8, pages 1071-1081.
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F. A. Hommes. (1985) Amino acidaemias and brain maturation: Interference with sulphate activation and myelin metabolism. Journal of Inherited Metabolic Disease 8:S2, pages 121-122.
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F. A. Hommes. 1985. Inherited Disorders of Vitamins and Cofactors. Inherited Disorders of Vitamins and Cofactors 121 122 .

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