Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra
- Author
- AKBAS, Nilgtin1 ; HOCHSTRASSER, Helmine1 ; DEPLAZES, Joelle1 ; TOMIUK, Jürgen2 ; BAUER, Peter1 ; WALTER, Uwe3 ; BEHNKE, Stefanie4 ; RIESS, Olaf1 ; BERG, Daniela5
[1] Institute of Medical Genetics, University of Tuebingen, Tuebingen, Germany
[2] Institute for Anthropology and Human Genetics, University of Tuebingen, Tuebingen, Germany
[3] Department of Neurology, University of Rostock, Rostock, Germany
[4] Department of Neurology, University of Homburg/Saar, Homburg/Saar, Germany
[5] Hertie Institue for Clinical Brain Research, University of Tuebingen, Hoppe-Seyler-Str. 3, Tuebingen 72076, Germany - Source
Neuroscience letters. 2006, Vol 407, Num 1, pp 16-19, 4 p ; ref : 22 ref
- CODEN
- NELED5
- ISSN
- 0304-3940
- Scientific domain
- Neurology; Physiology, morphology
- Publisher
- Elsevier, Shannon
- Publication country
- Ireland
- Document type
- Article
- Language
- English
- Author keyword
- Hemochromatosis gene (HFE) Iron metabolism Mutational screening Parkinson's disease Transcranial sonography
- Keyword (fr)
- Dépistage Fer Gène Homme Locus niger Mutation Métabolisme Parkinson maladie Déterminisme génétique Encéphale pathologie Extrapyramidal syndrome Génétique Maladie dégénérative Système nerveux central pathologie Système nerveux central Système nerveux pathologie
- Keyword (en)
- Medical screening Iron Gene Human Locus niger Mutation Metabolism Parkinson disease Genetic determinism Cerebral disorder Extrapyramidal syndrome Genetics Degenerative disease Central nervous system disease Central nervous system Nervous system diseases
- Keyword (es)
- Descubrimiento Hierro Gen Hombre Locus níger Mutación Metabolismo Parkinson enfermedad Determinismo genético Encéfalo patología Extrapiramidal síndrome Genética Enfermedad degenerativa Sistema nervosio central patología Sistema nervioso central Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A25 Vertebrates: nervous system and sense organs
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
- Discipline
- Neurology Vertebrates : nervous system and sense organs
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18176372
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/j.neulet.2006.07.070 
https://dx.doi.org/10.1016/j.neulet.2006.07.070
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