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Publications of P. Heutink
Articles in journal or book chapters
  1. C. F. Lippa, J. E. Duda, M. Grossman, H. I. Hurtig, D. Aarsland, B. F. Boeve, D. J. Brooks, D. W. Dickson, B. Dubois, M. Emre, S. Fahn, J. M. Farmer, D. Galasko, J. E. Galvin, C. G. Goetz, J. H. Growdon, K. A. Gwinn-Hardy, J. Hardy, P. Heutink, T. Iwatsubo, K. Kosaka, V. M. Lee, J. B. Leverenz, E. Masliah, I. G. McKeith, R. L. Nussbaum, C. W. Olanow, B. M. Ravina, A. B. Singleton, C. M. Tanner, J. Q. Trojanowski, and Z. K. Wszolek. DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers. Neurology, 68(11):812-9, 2007. Note: DLB/PDD Working GroupAG09215/AG/United States NIAAG10124/AG/United States NIANS054546-01/NS/United States NINDSJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, N.I.H., IntramuralResearch Support, Non-U.S. Gov'tReviewUnited States. [WWW] Keyword(s): Biological Markers/*metabolism, Humans, Lewy Body Disease/*diagnosis/metabolism/pathology/*therapy, Parkinson Disease/*diagnosis/metabolism/pathology/*therapy.


  2. V. Bonifati, P. Rizzu, F. Squitieri, E. Krieger, N. Vanacore, J. C. van Swieten, A. Brice, C. M. van Duijn, B. Oostra, G. Meco, and P. Heutink. DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism. Neurol Sci, 24(3):159-60, 2003. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tItalyofficial journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. [WWW] Keyword(s): *Chromosomes, Human, Pair 1, DNA Mutational Analysis, Family Health, Humans, Intracellular Signaling Peptides and Proteins, Mutation, Oncogene Proteins/*genetics, Parkinsonian Disorders/*genetics.


  3. V. Bonifati, P. Rizzu, M. J. van Baren, O. Schaap, G. J. Breedveld, E. Krieger, M. C. Dekker, F. Squitieri, P. Ibanez, M. Joosse, J. W. van Dongen, N. Vanacore, J. C. van Swieten, A. Brice, G. Meco, C. M. van Duijn, B. A. Oostra, and P. Heutink. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science, 299(5604):256-9, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Alleles, Amino Acid Sequence, Amino Acid Substitution, Animals, Base Sequence, Brain/metabolism, COS Cells, Cell Nucleus/metabolism, Chromosomes, Human, Pair 1, Cloning, Molecular, Cytoplasm/metabolism, DNA, Complementary, Exons, Genes, Recessive, Humans, Intracellular Signaling Peptides and Proteins, Molecular Sequence Data, *Mutation, Oncogene Proteins/chemistry/*genetics/metabolism, Oxidative Stress, PC12 Cells, Parkinsonian Disorders/*genetics/metabolism, Pedigree, Physical Chromosome Mapping, Point Mutation, Protein Structure, Secondary, Rats, Reverse Transcriptase Polymerase Chain Reaction, Sequence Deletion, Transfection.


  4. P. Ibanez, G. De Michele, V. Bonifati, E. Lohmann, S. Thobois, P. Pollak, Y. Agid, P. Heutink, A. Durr, and A. Brice. Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism. Neurology, 61(10):1429-31, 2003. Note: French Parkinson's Disease Genetics Study GroupNs41723-01a1/ns/nindsJournal ArticleResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.United States. [WWW] Keyword(s): Adolescent, Adult, Age of Onset, Aged, Child, DNA Mutational Analysis, Female, Gene Frequency, Genetic Predisposition to Disease, Humans, Intracellular Signaling Peptides and Proteins, Male, Middle Aged, *Mutation, Oncogene Proteins/*genetics, Parkinsonian Disorders/diagnosis/*genetics.



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