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106 Possible Causes for westaway

  • Tuberculosis

    Westaway, MS, Wolmarans, L. Cognitive and affective reactions of black urban South Africans towards tuberculosis . Tuber Lung Dis 1994 ;75: 447 – 53 .[doi.org]

  • Hallervorden-Spatz Syndrome

    Ching KHL, Westaway SK, Levinson B, Higgins JJ, Hayflick SJ.[rarediseases.org] Zhou B, Westaway SK, Levinson B, Johnson MA, Gischier J, Hayflick SJ. A novel Pantothenate Kinase gene is defective in Hallervorden Spatz syndrome.[link.springer.com] Zhou B, Westaway SK, Levinson B, Johnson MA, Gitschier J, Hayflick SJ. A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome.[ghr.nlm.nih.gov]

  • Neurodegeneration with Brain Iron Accumulation

    Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome Hayflick SJ, Westaway SK, Levinson B, Zhou B, Johnson MA, Ching KH, Gitschier J.[disorders.eyes.arizona.edu] Nat Genet. 1995; 9 :267–72. [ PubMed : 7539672 ] Zhou B, Westaway SK, Levinson B, Johnson MA, Gitschier J, Hayflick SJ.[ncbi.nlm.nih.gov] Hayflick SJ, Westaway SK, Levinson B, Zhou B, Johnson MA, Ching KH, Gitschier J. Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome .[disorders.eyes.arizona.edu]

  • HARP Syndrome

    Westaway , J. Gitschier , J. J. Higgins , S. J. Hayflick First published June 11, 2002, DOI: This article requires a subscription to view the full text.[neurology.org]

  • Infantile Neuroaxonal Dystrophy

    Morgan, NV, Westaway, SK, Morton, JE. PLA2G6 , encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron .[doi.org] Hayflick, MD Shawn Westaway, PhD Publications provided by PubMed discussing infantile neuroaxonal dystrophy (INAD): PubMed: INAD[ohsu.edu] Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome Hayflick SJ, Westaway SK, Levinson B, Zhou B, Johnson MA, Ching KH, Gitschier J.[disorders.eyes.arizona.edu]

  • Schindler Disease

    Westaway SK, Gregory A, Hayflick SJ. Mutations in PLA2G6 and the riddle of Schindler disease. J Med Genet. 2007;44:e64. Morgan NV, Westaway SK, Morton JEV, et al.[rarediseases.org] Mutations in PLA2G6 and the riddle of Schindler disease S K Westaway , A Gregory , S J Hayflick 1 Departments of Molecular and Medical Genetics, School of Medicine, Oregon[jmg.bmj.com] […] enzymes associated with Fabry and Schindler diseases. ( 20444686 ) Tomasic I.B....Garman S.C. 2010 5 Mutations in PLA2G6 and the riddle of Schindler disease. ( 17209134 ) Westaway[malacards.org]

  • Mitochondrial Membrane Protein-Associated Neurodegeneration

    Hayflick SJ, Westaway SK, Levinson B, Zhou B, Johnson MA, Ching KH, et al . Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.[pediatricneurosciences.com] Ching KHL, Westaway SK, Levinson B, Higgins JJ, Hayflick SJ.[rarediseases.org] Westaway, Ph.D., Barbara Levinson, M.A., Bing Zhou, Ph.D., Monique A. Johnson, Ph.D., Katherine H.L. Ching, B.S., and Jane Gitschier, Ph.D.[nejm.org]

  • Infantile Neuroaxonal Dystrophy 1

    ., Mohandas, T, DeArmond, SJ, Westaway, D., Prusiner, SB, and Weiner, LP (1986). Assignment of the human and mouse prion protein genes to homologous chromosomes. ‎[books.google.de] Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome Hayflick SJ, Westaway SK, Levinson B, Zhou B, Johnson MA, Ching KH, Gitschier J.[disorders.eyes.arizona.edu] Morgan NV, Westaway SK, Morton JE, Gregory A, Gissen P, Sonek S, Cangul H, Coryell J, Canham N, Nardocci N, Zorzi G, Pasha S, Rodriguez D, Desguerre I, Mubaidin A, Bertini[ghr.nlm.nih.gov]

  • Schindler Disease, Type 1

    Westaway SK, Gregory A, Hayflick SJ. Mutations in PLA2G6 and the riddle of Schindler disease. J Med Genet. 2007;44:e64. Morgan NV, Westaway SK, Morton JEV, et al.[rarediseases.org]

  • ADan Amyloidosis

    ., Westaway D. and Kretzschmar H. (1997a) The cellular prion protein binds copper in vivo. ‎[books.google.de]

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