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Connection

James A. Mastrianni to Phenotype

This is a "connection" page, showing publications James A. Mastrianni has written about Phenotype.
Connection Strength

0.301
  1. The prion diseases. J Geriatr Psychiatry Neurol. 2010 Dec; 23(4):277-98.
    View in: PubMed
    Score: 0.060
  2. A New Transgenic Mouse Model of Gerstmann-Straussler-Scheinker Syndrome Caused by the A117V Mutation of PRNP. J Neurosci. 2009 Aug 12; 29(32):10072-80.
    View in: PubMed
    Score: 0.056
  3. Prion protein codon 129 genotype prevalence is altered in primary progressive aphasia. Ann Neurol. 2005 Dec; 58(6):858-64.
    View in: PubMed
    Score: 0.043
  4. Inherited prion disease caused by the V210I mutation: transmission to transgenic mice. Neurology. 2001 Dec 26; 57(12):2198-205.
    View in: PubMed
    Score: 0.033
  5. The prion diseases. Semin Neurol. 2000; 20(3):337-52.
    View in: PubMed
    Score: 0.029
  6. IVIG Delays Onset in a Mouse Model of Gerstmann-Sträussler-Scheinker Disease. Mol Neurobiol. 2019 Apr; 56(4):2353-2361.
    View in: PubMed
    Score: 0.026
  7. The prion diseases: Creutzfeldt-Jakob, Gerstmann-Sträussler-Scheinker, and related disorders. J Geriatr Psychiatry Neurol. 1998; 11(2):78-97.
    View in: PubMed
    Score: 0.025
  8. Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype. Ann Neurol. 2011 Apr; 69(4):712-20.
    View in: PubMed
    Score: 0.016
  9. Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. Ann Neurol. 2010 Aug; 68(2):162-72.
    View in: PubMed
    Score: 0.015
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.