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There are 5670 results for: content related to: Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia

  1. How well do caregivers detect mild cognitive change in Parkinson's disease?

    Movement Disorders

    Volume 26, Issue 1, January 2011, Pages: 161–164, Sharon L. Naismith, Marilia Pereira, James M. Shine and Simon J.G. Lewis

    Article first published online : 3 SEP 2010, DOI: 10.1002/mds.23331

  2. Silent saliva aspiration in Parkinson's disease

    Movement Disorders

    Volume 26, Issue 1, January 2011, Pages: 138–141, Bernardo Rodrigues, Ana Caline Nóbrega, Marília Sampaio, Natalie Argolo and Ailton Melo

    Article first published online : 16 NOV 2010, DOI: 10.1002/mds.23301

  3. Cerebrospinal fluid tau and phosphorylated tau protein are elevated in corticobasal syndrome

    Movement Disorders

    Volume 26, Issue 1, January 2011, Pages: 169–173, M.B. Aerts, R.A.J. Esselink, B.R. Bloem and M.M. Verbeek

    Article first published online : 10 SEP 2010, DOI: 10.1002/mds.23341

  4. Tardive dyskinesia and other movement disorders secondary to aripiprazole

    Movement Disorders

    Volume 26, Issue 1, January 2011, Pages: 147–152, Maria Sierra Peña, Toby C. Yaltho and Joseph Jankovic

    Article first published online : 3 SEP 2010, DOI: 10.1002/mds.23402

  5. Apomorphine effect on pain threshold in Parkinson's disease: A clinical and positron emission tomography study

    Movement Disorders

    Volume 26, Issue 1, January 2011, Pages: 153–157, Estelle Dellapina, Angélique Gerdelat-Mas, Fabienne Ory-Magne, Laure Pourcel, Monique Galitzky, Fabienne Calvas, Marion Simonetta-Moreau, Claire Thalamas, Pierre Payoux and Christine Brefel-Courbon

    Article first published online : 19 OCT 2010, DOI: 10.1002/mds.23406

  6. Use of smell test identification in Parkinson's disease in Mexico: A matched case-control study

    Movement Disorders

    Volume 26, Issue 1, January 2011, Pages: 173–176, Mayela Rodríguez-Violante, Andrew J. Lees, Amin Cervantes-Arriaga, Teresa Corona and Laura Silveira-Moriyama

    Article first published online : 14 SEP 2010, DOI: 10.1002/mds.23354

  7. Reduced but not oxidized cerebrospinal fluid glutathione levels are lowered in Lewy body diseases

    Movement Disorders

    Volume 26, Issue 1, January 2011, Pages: 176–181, Walter Maetzler, Stefan P. Schmid, Isabel Wurster, Inga Liepelt, Alexandra Gaenslen, Thomas Gasser and Daniela Berg

    Article first published online : 14 SEP 2010, DOI: 10.1002/mds.23358

  8. Estimation of skeletal muscle energy metabolism in Machado-Joseph disease using 31P-MR spectroscopy

    Movement Disorders

    Volume 26, Issue 1, January 2011, Pages: 165–168, Ichiro Yabe, Khin K. Tha, Takashi Yokota, Kazunori Sato, Hiroyuki Soma, Asako Takei, Satoshi Terae, Koichi Okita and Hidenao Sasaki

    Article first published online : 3 SEP 2010, DOI: 10.1002/mds.23335

  9. Regional cortical grey matter loss in Parkinson's disease without dementia is independent from visual hallucinations

    Movement Disorders

    Volume 26, Issue 1, January 2011, Pages: 142–147, Anne Marthe Meppelink, Bauke M. de Jong, Laura K. Teune and Teus van Laar

    Article first published online : 4 OCT 2010, DOI: 10.1002/mds.23375

  10. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S1–S523,

    Article first published online : 19 JUN 2012, DOI: 10.1002/mds.25051

  11. Chronic Hyperphenylalaninemia Produces Cerebral Hyperglycinemia in Immature Rats

    Journal of Neurochemistry

    Volume 36, Issue 1, January 1981, Pages: 34–43, Gerald A. Dienel

    Article first published online : 5 OCT 2006, DOI: 10.1111/j.1471-4159.1981.tb02374.x

  12. The frequency of PKU and hyperphenylalaninemia in Sweden - a study in institutions for the mentally retarded as well as in neonates

    Clinical Genetics

    Volume 10, Issue 5, November 1976, Pages: 313–318, Gösta Holmgren, Agne Larsson, Hans Palmstierna and Jan Alm

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1976.tb00054.x

  13. Dominant negative allele (N47D) in a compound heterozygote for a variant of 6-pyruvoyltetrahydropterin synthase deficiency causing transient hyperphenylalaninemia

    Human Mutation

    Volume 13, Issue 4, 1999, Pages: 286–289, Tanja Scherer-Oppliger, Ana Matasovic, Stephanie Laufs, Harvey L. Levy, Elisabeth J. Quackenbush, Nenad Blau and Beat Thöny

    Article first published online : 31 MAR 1999, DOI: 10.1002/(SICI)1098-1004(1999)13:4<286::AID-HUMU4>3.0.CO;2-C

  14. Maternal hyperphenylalaninemia: An experimental model in rats

    Developmental Psychobiology

    Volume 9, Issue 2, March 1976, Pages: 157–166, Arnold Andersen

    Article first published online : 13 OCT 2004, DOI: 10.1002/dev.420090208

  15. PERSISTENT HYPERPHENYLALANINEMIA

    Acta Paediatrica

    Volume 61, Issue 3, May 1972, Pages: 321–328, F. GÜTTLER and E. WAMBERG

    Article first published online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1972.tb16107.x

  16. Effect of α-Methylphenylalanine and Phenylalanine on Brain Polyribosomes and Protein Synthesis

    Journal of Neurochemistry

    Volume 36, Issue 4, April 1981, Pages: 1476–1484, Patricia A Binek, Terry C Johnson and Chester J Kelly

    Article first published online : 5 OCT 2006, DOI: 10.1111/j.1471-4159.1981.tb00589.x

  17. 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

    Article first published online : 12 NOV 2008, DOI: 10.1111/j.1469-8749.1969.tb01515.x

  18. You have free access to this content
    Mutation spectrum in Taiwanese patients with phenylalanine hydroxylase deficiency and a founder effect for the R241C mutation

    Human Mutation

    Volume 23, Issue 2, February 2004, Page: 206, Yin-Hsiu Chien, Shu-Chuan Chiang, Aichu Huang, Shi-Ping Chou, Szu-San Tseng, Yuan-Te Huang and Wuh-Liang Hwu

    Article first published online : 8 JAN 2004, DOI: 10.1002/humu.9215

  19. Transient Neonatal Hyperphenylalaninemia due to Immature Development of 7, 8-Dihydrobiopterin Synthesis

    Pediatrics International

    Volume 26, Issue 4, December 1984, Pages: 561–564, Yoshitomo Sawada, Haruo Shintaku, Gen Isshiki, Yutaka Hase, Tsuneo Tsuruhara and Toshiaki Oura

    Article first published online : 9 OCT 2007, DOI: 10.1111/j.1442-200X.1984.tb01863.x

  20. Mutations in the phenylalanine hydroxylase gene: genetic determinants for the phenotypic variability of hyperphenylalaninemia

    Acta Paediatrica

    Volume 83, Issue s407, December 1994, Pages: 49–56, F Güttler and P Guldberg

    Article first published online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1994.tb13451.x