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

Index « ISSN » - entrée « 0148-7299 »
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0148-639X < 0148-7299 < 0149-2918  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 16.
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
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
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
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
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
001739 (1997) Alain Verloes ; Martial Massin ; Jacques Lombet ; Bettina Grattagliano ; Daniel Soyeur ; Jacques Rigo ; Lucien Koulischer ; François Van HoofNosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form
001B49 (1999) Pierre Chagnon ; Mark Gee ; Mario Filion ; Yves Robitaille ; Majid Belouchi ; Denis GauvreauPhylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French‐Canadian founder population
002311 (1997) Paola Costa ; Harvey Checkoway ; Drew Levy ; Terri Smith-Weller ; Gary M. Franklin ; Phillip D. Swanson ; Lucio G. CostaAssociation of a polymorphism in intron 13 of the monoamine oxidase B gene with Parkinson disease
002807 (1999) Deborah E. Schuback ; Evan L. Mulligan ; Katherine B. Sims ; Elizabeth A. Tivol ; Benjamin D. Greenberg ; Shu-Fen Chang ; Show-Lin Yang ; Yi-Chien Mau ; Chen-Yang Shen ; Mei-Shang Ho ; Nan-Hua Yang ; Merlin G. Butler ; Stephen Fink ; Charles E. Schwartz ; F. Berlin ; Xandra O. Breakefield ; Dennis L. Murphy ; Yun-Pung Paul HsuScreen for MAOA mutations in target human groups
002A18 (1995) John HardyApolipoprotein E in the genetics and epidemiology of Alzheimer's disease
002E87 (1995) Campion ; M. Martinez ; D. Hannequin ; A. Brice ; C. Thomas-Anterion ; A. Michon ; M. C. Babron ; B. Dubois ; Y. Goas ; A. Jaillard-Serradt ; F. Ledoze ; F. Pasquier ; M. Puel ; M. A. Zimmerman ; M. Bellis ; J. Mallet ; Y. Agid ; F. Clerget-DarpouxCharacteristics of familial aggregation in early‐onset Alzheimer's disease: Evidence of subgroups

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