Serveur d'exploration sur la maladie de Parkinson - Corpus (Accueil)

Index « ISSN » - entrée « Am. J. Med. Genet. »
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Am. J. Ind. Med. < Am. J. Med. Genet. < Ann Biomed Eng  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 49.
[0-20] [0 - 20][0 - 49][20-40]
Ident.Authors (with country if any)Title
000008 (2002) Sepideh Zareparsi ; Richard Camicioli ; Gary Sexton ; Thomas Bird ; Phillip Swanson ; Jeffrey Kaye ; John Nutt ; Haydeh PayamiAge at onset of Parkinson disease and apolipoprotein E genotypes
000137 (2002) N. E. Maher ; L. J. Currie ; A. M. Lazzarini ; J. B. Wilk ; C. A. Taylor ; M. H. Saint-Hilaire ; R. G. Feldman ; L. I. Golbe ; G. F. Wooten ; R. H. MyersSegregation analysis of Parkinson disease revealing evidence for a major causative gene
000202 (1996) G. Lucotte ; J. Turpin ; N. Gérard ; S. Panserat ; R. KrishnamoorthyMutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in families
000213 (2002) Guomei Tang ; Huijun Xie ; Lin Xu ; Yixin Hao ; Dayu Lin ; Daming RenGenetic study of Apolipoprotein E gene, alpha‐1 antichymotrypsin gene in sporadic Parkinson disease
000529 (2006) Brad A. Racette ; Laura Good ; Jo Ann Antenor ; Lori Mcgee-Minnich ; Stephen M. Moerlein ; Tom O. Videen ; Joel S. Perlmutter[18F]FDOPA PET as an endophenotype for Parkinson's Disease linkage studies
000567 (2010) Yih-Ru Wu ; Chun-Hsien Wu ; Chih-Ying Chao ; Chun-Chieh Kuan ; Wan-Ling Zhang ; Cheng-Kuang Wang ; Chun-Yuh Chang ; Yi-Chun Chang ; Guey-Jen Lee-Chen ; Chung-Mei ChenGenetic analysis of Parkin in early onset Parkinson's disease (PD): Novel intron 9 g > a single nucleotide polymorphism and risk of Taiwanese PD
000896 (2008) Michael S. Hildebrand ; Jessica L. Sorensen ; Maren Jensen ; William J. Kimberling ; Richard J. H. SmithAutoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1
000972 (2011) Angela Scheuerle ; Kathleen WilsonPARK2 copy number aberrations in two children presenting with autism spectrum disorder: Further support of an association and possible evidence for a new microdeletion/microduplication syndrome
000A62 (2002) Andrew West ; Magali Periquet ; Sarah Lincoln ; Christoph B. Lücking ; David Nicholl ; Vincenzo Bonifati ; Nina Rawal ; Thomas Gasser ; Ebba Lohmann ; Jean-François Deleuze ; Demetrius Maraganore ; Allan Levey ; Nick Wood ; Alexandra Dürr ; John Hardy ; Alexis Brice ; Matt FarrerComplex relationship between Parkin mutations and Parkinson disease
000C02 (1999) C. A. Taylor ; M. H. Saint-Hilaire ; L. A. Cupples ; C. A. Thomas ; A. E. Burchard ; R. G. Feldman ; R. H. MyersEnvironmental, medical, and family history risk factors for Parkinson's disease: A New England‐based case control study
000C91 (2007) Chiung-Mei Chen ; I-Cheng Chen ; Kuo-Hsuan Chang ; Yi-Chun Chen ; Rong-Kuo Lyu ; Yen-Tzu Liu ; Fen-Ju Hu ; Chih-Ying Chao ; Guey-Jen Lee-Chen ; Yih-Ru WuNuclear receptor NR4A2 IVS6 +18insG and brain derived neurotrophic factor (BDNF) V66M polymorphisms and risk of Taiwanese parkinson's disease
000D19 (2011) Chiung-Mei Chen ; Chih-Hsin Lin ; Hsueh-Fen Juan ; Fen-Ju Hu ; Ya-Chin Hsiao ; Hsin-Yi Chang ; Chih-Ying Chao ; I-Cheng Chen ; Li-Ching Lee ; Tsu-Wei Wang ; Ya-Tang Chen ; Yi-Tsun Chen ; Guey-Jen Lee-Chen ; Yih-Ru WuATP13A2 variability in Taiwanese Parkinson's disease
000E38 (2003) Andrea Carmine ; Silvia Buervenich ; Dagmar Galter ; Erik G. Jönsson ; Göran C. Sedvall ; Lars Farde ; J. Petter Gustavsson ; Hans Bergman ; Kodavali V. Chowdari ; Vishwajit L. Nimgaonkar ; Maria Anvret ; Olof Sydow ; Lars OlsonNURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits
000E82 (2001) M. Orth ; A. H. V. SchapiraMitochondria and degenerative disorders
000F96 (1998) Sepideh Zareparsi ; Todd D. Taylor ; Emily L. Harris ; Haydeh PayamiSegregation analysis of Parkinson disease
001088 (2010) Stephan Klebe ; Sandra Thier ; Delia Lorenz ; Michael Nothnagel ; Stefan Schreiber ; Christine Klein ; Johann Hagenah ; Meike Kasten ; Daniela Berg ; Karin Srulijes ; Thomas Gasser ; Günther Deuschl ; Gregor Kuhlenb UmerLINGO1 is not associated with Parkinson's disease in German patients
001121 (1996) Michael D. Brown ; John M. Shoffner ; Yoon L. Kim ; Albert S. Jun ; Brett H. Graham ; Margaret F. Cabell ; Daniel S. Gurley ; Douglas C. WallaceMitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patients
001196 (2006) M. A. Slifer ; E. R. Martin ; P. G. Bronson ; C. Browning-Large ; P. M. Doraiswamy ; K. A. Welsh-Bohmer ; J. R. Gilbert ; J. L. Haines ; M. A. Pericak-VanceLack of association between UBQLN1 and Alzheimer disease
001319 (2002) P. Volders ; J. Van Hove ; R. J. U. Lories ; Ph. Vandekerckhove ; G. Matthijs ; R. De Vos ; M. T. Vanier ; M. F. Vincent ; R. Westhovens ; F. P. LuytenNiemann‐Pick disease type B: An unusual clinical presentation with multiple vertebral fractures
001326 (2003) Judit Várkonyi ; Hanna Rosenbaum ; Nicole Baumann ; Jennifer J. Mackenzie ; Zsuzsa Simon ; Judith Aharon-Peretz ; Jamie M. Walker ; Nahid Tayebi ; Ellen SidranskyGaucher disease associated with parkinsonism: Four further case reports
001425 (2008) Denise M. Kay ; Stewart A. Factor ; Ali Samii ; Donald S. Higgins ; Alida Griffith ; John W. Roberts ; Berta C. Leis ; John G. Nutt ; Jennifer S. Montimurro ; Robert G. Keefe ; April J. Atkins ; Dora Yearout ; Cyrus P. Zabetian ; Haydeh PayamiGenetic association between α‐synuclein and idiopathic parkinson's disease

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