La maladie de Parkinson en France (serveur d'exploration) - Analysis (UK)

Index « Auteurs » - entrée « Giuseppe De Michele »
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Giuseppe Capovilla < Giuseppe De Michele < Giuseppe Demichele  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 8.
Ident.Authors (with country if any)Title
000503 (2005) Maria Martinez [France] ; Alexis Brice [France] ; Jenny R. Vaughan [Royaume-Uni] ; Alexander Zimprich [Allemagne] ; Monique M. B. Breteler [Pays-Bas] ; Giuseppe Meco [Italie] ; Alessandro Filla [Italie] ; Matthew J. Farrer [États-Unis] ; Christine Bétard [France] ; Andrew Singleton [États-Unis] ; John Hardy [États-Unis] ; Giuseppe De Michele [Italie] ; Vincenzo Bonifati [Italie] ; Ben A. Oostra [Pays-Bas] ; Thomas Gasser [Allemagne] ; Nick W. Wood [Royaume-Uni] ; Alexandra Dürr [France]Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease
000513 (2005) Maria Martinez [France] ; Alexis Brice [France] ; Jenny R. Vaughan [Royaume-Uni] ; Alexander Zimprich [Allemagne] ; Monique M. B. Breteler [Pays-Bas] ; Giuseppe Meco [Italie] ; Alessandro Filla [Italie] ; Matthew J. Fatter [États-Unis] ; Christine Betard [France] ; Andrew Singleton [États-Unis] ; John Hardy [États-Unis] ; Giuseppe De Michele [Italie] ; Vincenzo Bonifati [Italie] ; Ben A. Oostra [Pays-Bas] ; Thomas Gasser [Allemagne] ; Nick W. Wood [Royaume-Uni] ; Alexandra Dürr [France]Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease
000544 (2003) Magali Periquet ; Morwena Latouche ; Ebba Lohmann ; Nina Rawal ; Giuseppe De Michele ; Sylvain Ricard ; He Lio Teive ; Vale Rie Fraix ; Marie Vidailhet ; David Nicholl ; Paolo Barone ; Nick W. Wood [Royaume-Uni] ; Salmo Raskin ; Jean-Franc Ois Deleuze ; Yves Agid [France] ; Alexandra Du Rr ; Alexis BriceParkin mutations are frequent in patients with isolated early‐onset parkinsonism
000546 (2003) Ebba Lohmann [France] ; Magali Periquet [France] ; Vincenzo Bonifati [Italie] ; Nick W. Wood [Royaume-Uni] ; Giuseppe De Michele [Italie] ; Anne-Marie Bonnet [France] ; Valérie Fraix [France] ; Emmanuel Broussolle [France] ; Martin W. I. M. Horstink [Pays-Bas] ; Marie Vidailhet [France] ; Patrice Verpillat [France] ; Thomas Gasser [Allemagne] ; David Nicholl [Royaume-Uni] ; Hélio Teive [Brésil] ; Salmo Raskin [Brésil] ; Olivier Rascol ; Alain Destée [France] ; Merle Ruberg [France] ; Francesca Gasparini [France] ; Giuseppe Meco [Italie] ; Yves Agid [France] ; Alexandra Durr [France] ; Alexis Brice [France]How much phenotypic variation can be attributed to parkin genotype?
000553 (2002) Enza Maria Valente [Italie, Royaume-Uni] ; Francesco Brancati [Italie] ; Alessandro Ferraris [Italie] ; Elizabeth A. Graham [Royaume-Uni] ; Mary B. Davis [Royaume-Uni] ; Monique M. B. Breteler [Pays-Bas] ; Thomas Gasser [Allemagne] ; Vincenzo Bonifati [Italie] ; Anna Rita Bentivoglio [Italie] ; Giuseppe De Michele [Italie] ; Alexandra Dürr [France] ; Pietro Cortelli [Italie] ; Dietmar Wassilowsky [Allemagne] ; Biswadjiet S. Harhangi [Pays-Bas] ; Nina Rawal [France] ; Viviana Caputo [Italie] ; Alessandro Filla [Italie] ; Giuseppe Meco [Italie] ; Ben A. Oostra [Pays-Bas] ; Alexis Brice [France] ; Alberto Albanese [Italie] ; Bruno Dallapiccola [Italie] ; Nicholas W. Wood [Royaume-Uni]Park6‐linked parkinsonism occurs in several european families
000615 (1999) Nacer Abbas [France] ; Christoph B. Lücking [France] ; Sylvain Ricard [France] ; Alexandra Dürr [France] ; Vincenzo Bonifati [Italie] ; Giuseppe De Michele [Italie] ; Sandrine Bouley [France] ; Jenny R. Vaughan [Royaume-Uni] ; Thomas Gasser [Allemagne] ; Roberto Marconi [Italie] ; Emmanuel Broussolle [France] ; Christine Brefel-Courbon [France] ; Biswadjiet S. Harhangi [Pays-Bas] ; Ben A. Oostra [Pays-Bas] ; Edito Fabrizio [Italie] ; Georg A. Böhme [France] ; Laurent Pradier [France] ; Nick W. Wood [Royaume-Uni] ; Alessandro Filla [Italie] ; Giuseppe Meco [Italie] ; Patrice Denefle [France] ; Yves Agid [France] ; Alexis Brice [France]A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe
000617 (1999) B. Sanjay Harhangi [Pays-Bas] ; Matthew J. Farrer [États-Unis] ; Sarah Lincoln [États-Unis] ; Vincenzo Bonifati [Italie] ; Giuseppe Meco [Italie] ; Giuseppe De Michele [Italie] ; Alexis Brice [France] ; Alexandra Dürr [France] ; Maria Martinez [France] ; Thomas Gasser [Allemagne] ; Benjamin Bereznai [Allemagne] ; Jenny R. Vaughan [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] ; John Hardy [États-Unis] ; Ben A. Oostra [Pays-Bas] ; Monique M. B. Breteler [Pays-Bas]The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease
000634 (1998) Jenny Vaughan [Royaume-Uni] ; Alexandra Durr [France] ; Johann Tassin [France] ; Benjamin Bereznai [Allemagne] ; Thomas Gasser [Allemagne] ; Vincenzo Bonifati [Italie] ; Giuseppe De Michele [Italie] ; Edito Fabrizio [Italie] ; Gianpiero Volpe [Italie] ; O. Bandmann [Royaume-Uni] ; William G. Johnson [États-Unis] ; Lawrence I. Golbe [États-Unis] ; Monique Breteler [Pays-Bas] ; Giuseppe Meco [France] ; Yves Agid [France] ; Alexis Brice [Royaume-Uni] ; C. David Marsden [Royaume-Uni] ; C. David Wood [Royaume-Uni]The α‐synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases

List of associated KwdEn.i

Nombre de
documents
Descripteur
6Human
6Parkinson disease
4Humans
4Mutation
4Parkinson Disease (genetics)
3Female
3Genetics
3Genotype
3Male
3Phenotype
2Aged
2Exons (genetics)
2Family Health
2Family study
2Gene
2Genetic determinism
2Middle Aged
2Parkinson's disease
2Point Mutation
1Abbreviations: PCR = polymerase chain reaction
1Adolescent
1Adult
1Age of Onset
1Age of onset
1Aged, 80 and over
1Alleles
1Amino Acid Substitution
1Antiparkinson Agents (therapeutic use)
1Apolipoprotein E
1Apolipoprotein E4
1Apolipoproteins E (genetics)
1Autosomal character
1Binding Sites
1Candidate gene
1Chromosome C6
1Chromosome F19
1Chromosomes, Human, Pair 19 (genetics)
1DNA Primers
1Disease Progression
1Dystonia
1Etiopathogenesis
1Europe
1European
1European Continental Ancestry Group (genetics)
1Exons
1Exploration
1Family studies
1France
1Gene Deletion
1Gene Frequency
1Genes, Recessive (genetics)
1Genetic Linkage
1Genetic Variation (genetics)
1Genetic linkage
1Genetic mapping
1Germany
1Haplotype
1Heterozygote
1Homozygosity
1Idiopathic
1Italy
1Keywords: parkin; mutation frequency; isolated early‐onset parkinsonism
1Levodopa (therapeutic use)
1Ligases
1Linkage Disequilibrium
1Lod Score
1Microsatellite Repeats
1Molecular biology
1Mutation (genetics)
1Mutation, Missense (genetics)
1Nerve Tissue Proteins (genetics)
1Netherlands
1Nuclear Family
1Parkinson Disease (drug therapy)
1Parkinson Disease (enzymology)
1Parkinson Disease (physiopathology)
1Parkinsonism
1Pathogenesis
1Pathophysiology
1Pedigree
1Polymerase Chain Reaction
1Polymerase chain reaction
1Polymorphism
1Polymorphism, Genetic
1Proteins (genetics)
1Recessive character
1Siblings
1Sporadic
1Thiolester Hydrolases (chemistry)
1Thiolester Hydrolases (genetics)
1Ubiquitin Thiolesterase
1Ubiquitin thiolesterase
1Ubiquitin-Protein Ligases
1Ubiquitin-Protein Ligases (genetics)
1Ubiquitin-carboxy-terminal-hydrolase-L1
1apolipoprotein E
1genetics

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