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There are 14094 results for: content related to: Inhibition by l -Phenylalanine of Tyrosine Transport by Synaptosomal Plasma Membrane Vesicles: Implications in the Pathogenesis of Phenylketonuria

  1. Heterozygote detection in phenylketonuria

    Clinical Genetics

    Volume 11, Issue 2, February 1977, Pages: 137–146, Flemming Güttler and Gert Hansen

    Version of Record online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1977.tb01291.x

  2. You have free access to this content
    The PAH gene, phenylketonuria, and a paradigm shift

    Human Mutation

    Volume 28, Issue 9, September 2007, Pages: 831–845, Charles R. Scriver

    Version of Record online : 18 APR 2007, DOI: 10.1002/humu.20526

  3. Another Population of Phenylketonuria? Studies on Atypical Phenylketonurias

    Developmental Medicine & Child Neurology

    Volume 11, Issue 6, December 1969, Pages: 718–729, Paul Dyken and William Culley

    Version of Record online : 12 NOV 2008, DOI: 10.1111/j.1469-8749.1969.tb01515.x

  4. REFERENCES

    Acta Paediatrica

    Volume 69, Issue S280, April 1980, Pages: 74–80,

    Version of Record online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1980.tb06211.x

  5. Disorders of Amino Acid Metabolism, Organic Acidaemias and Urea Cycle Defects

    Clinical Paediatric Dietetics, Third Edition

    Anita MacDonald, Marjorie Dixon, Fiona White, Pages: 310–389, 2008

    Published Online : 15 APR 2008, DOI: 10.1002/9780470692004.ch17

  6. The Metabolism of Indole-Compounds in Phenylketonuria

    Developmental Medicine & Child Neurology

    Volume 3, Issue 3, June 1961, Pages: 237–243, DAVID YI-YUNG HSIA and IRENE HUANG

    Version of Record online : 12 NOV 2008, DOI: 10.1111/j.1469-8749.1961.tb10374.x

  7. 5-Hydroxyindole Levels in the Blood and CSF in Down's Syndrome, Phenylketonuria and Severe Mental Retardation

    Developmental Medicine & Child Neurology

    Volume 14, Issue 4, August 1972, Pages: 457–466, Junbi Tu and M. W. Partington

    Version of Record online : 12 NOV 2008, DOI: 10.1111/j.1469-8749.1972.tb02618.x

  8. Phenylketonuria 1967

    Developmental Medicine & Child Neurology

    Volume 9, Issue 5, October 1967, Pages: 531–540, David Yi-Yung Hsia

    Version of Record online : 12 NOV 2008, DOI: 10.1111/j.1469-8749.1967.tb02321.x

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    Sapropterin dihydrochloride for phenylketonuria

    Intervention Review

    The Cochrane Library

    Usha Rani Somaraju and Marcus Merrin

    Published Online : 27 MAR 2015, DOI: 10.1002/14651858.CD008005.pub4

  10. The Phenylalanine Hydroxylase Locus: A Marker for the History of Phenylketonuria and Human Genetic Diversity

    Ciba Foundation Symposium 197 - Variation in the Human Genome

    Charles R. Scriver, Susan Byck, Lynne Prevost, Liem Hoang, Pages: 73–96, 2007

    Published Online : 28 SEP 2007, DOI: 10.1002/9780470514887.ch5

  11. Effectiveness of Dietary Treatment in Phenylketonuria: What is the Proof?

    Developmental Medicine & Child Neurology

    Volume 9, Issue 4, August 1967, Pages: 411–418, Phyllis W. Herman, Harry A. Waisman and Frances K. Graham.

    Version of Record online : 12 NOV 2008, DOI: 10.1111/j.1469-8749.1967.tb02293.x

  12. Phenylketonuria as a balanced polymorphism: the nature of the heterozygote advantage

    Annals of Human Genetics

    Volume 38, Issue 4, May 1975, Pages: 461–469, L. I. WOOLF, M. S. McBEAN, F. M. WOOLF and S. F. CAHALANF

    Version of Record online : 28 SEP 2007, DOI: 10.1111/j.1469-1809.1975.tb00635.x

  13. METABOLIC DISORDERS

    Developmental Medicine & Child Neurology

    Volume 13, Issue s23, February 1971, Pages: 76–83,

    Version of Record online : 12 NOV 2008, DOI: 10.1111/j.1469-8749.1971.tb03084.x

  14. Biochemical markers associated with executive function in adolescents with early and continuously treated phenylketonuria

    Clinical Genetics

    Volume 75, Issue 2, February 2009, Pages: 169–174, R Sharman, K Sullivan, R Young and J McGill

    Version of Record online : 30 DEC 2008, DOI: 10.1111/j.1399-0004.2008.01101.x

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    PHENYLKETONURIA: DATA ON FORTY-SEVEN BRITISH FAMILIES

    Annals of Eugenics

    Volume 14, Issue 1, January 1947, Pages: 60–88, T. A. MUNRO

    Version of Record online : 13 APR 2011, DOI: 10.1111/j.1469-1809.1947.tb02379.x

  16. PHENYLKETONURIA:

    Journal of Intellectual Disability Research

    Volume 1, Issue 1, July 1957, Pages: 53–65, DAVID YI-YUNG HSIA, RICHMOND S. PAINE and KATHLEEN W. DRISCOLL

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1365-2788.1957.tb00280.x

  17. Repeated adverse fetal outcome in pregnancy complicated by uncontrolled maternal phenylketonuria

    Journal of Paediatrics and Child Health

    Volume 35, Issue 5, October 1999, Pages: 499–502, GJ Kesby

    Version of Record online : 19 JUN 2002, DOI: 10.1046/j.1440-1754.1999.355370.x

  18. Factors affecting cognitive, motor, behavioral and executive functioning in children with phenylketonuria

    Acta Paediatrica

    Volume 87, Issue 5, May 1998, Pages: 565–570, GL Arnold, BM Kramer, RS Kirby, PB Plumeau, EM Blakely, LS Sanger Cregan and PW Davidson

    Version of Record online : 2 JAN 2007, DOI: 10.1111/j.1651-2227.1998.tb01505.x

  19. FOLLOW-UP NOTE ON AN ATYPICAL CASE OF PHENYLKETONURIA

    Journal of Intellectual Disability Research

    Volume 2, Issue 2, December 1958, Pages: 55–58, VALERIE COWIE and M. W. GILLIAN BRANDON

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1365-2788.1958.tb00386.x

  20. You have free access to this content
    Phenylketonuria mutations in Europe

    Human Mutation

    Volume 21, Issue 4, April 2003, Pages: 345–356, Johannes Zschocke

    Version of Record online : 19 MAR 2003, DOI: 10.1002/humu.10192