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Association between conformational mutations in neuroserpin and onset and severity of dementia

Author
DAVIS, Richard L1 ; SHRIMPTON, Antony E1 ; PICCARDO, Pedro9 ; TAKAO, Masaki9 ; LACBAWAN, Felicitas10 11 ; MUENKE, Maximilian11 ; SIFERS, Richard N12 ; BRADSHAW, Charles B13 ; KENT, Paul F13 ; COLLINS, George H1 ; LAROCCA, Daria14 ; HOLOHAN, Peter D14 ; CARRELL, Robin W2 ; LOMAS, David A2 3 ; GERHARD, Lieselotte4 ; BAUMANN, Bruno5 ; LAWRENCE, Daniel A6 ; YEPES, Manuel6 7 ; TAI SEUNG KIM8 ; GHETTI, Bernardino9
[1] Department of Pathology, Upstate Medical University, Syracuse, NY, United States
[2] Department of Haematology, University of Cambridge, Cambridge, United Kingdom
[3] Department of Medicine, University of Cambridge, Cambridge Institute for Medical Research, Cambridge, United Kingdom
[4] Institute for Clinical Neurosurgery, University of Witten-Herdecke, Germany
[5] Department of Psychiatry, University of Magdeburg, Magdeburg, Germany
[6] Department of Vascular Biology, American Red Cross Holland Laboratory, Rockville, MD, United States
[7] Department of Neurology, Georgetown University Medical Center, Washington, DC, United States
[8] Department of Pathology, Yonsei University College of Medicine, Seoul, Korea, Republic of
[9] Alzheimer Disease Center, Division of Neuropathology, Indiana University School of Medicine, Indianapolis, IN, United States
[10] Department of Medical Genetics, Children's National Medical Center, Washington, DC, United States
[11] Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States
[12] Department of Pathology, Baylor College of Medicine, Houston, TX, United States
[13] Department of Neurology, Upstate Medical University, Syracuse, NY, United States
[14] Department of Pharmacology, Upstate Medical University, Syracuse, NY, United States
Source

Lancet (British edition). 2002, Vol 359, Num 9325, pp 2242-2247 ; ref : 33 ref

CODEN
LANCAO
ISSN
0140-6736
Scientific domain
General medicine general surgery
Publisher
Lancet, London
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Conformation Corps inclusion Démence Déterminisme génétique Encéphalopathie Etude familiale Génétique Homme Maladie familiale Mutation Pathogénie Protéine Corps Collins Neuroserpine Encéphale pathologie Maladie dégénérative Système nerveux central pathologie Système nerveux pathologie
Keyword (en)
Conformation Inclusion body Dementia Genetic determinism Encephalopathy Family study Genetics Human Familial disease Mutation Pathogenesis Protein Cerebral disorder Degenerative disease Central nervous system disease Nervous system diseases
Keyword (es)
Conformación Cuerpo inclusión Demencia Determinismo genético Encefalopatía Estudio familiar Genética Hombre Enfermedad familiar Mutación Patogenia Proteína Encéfalo patología Enfermedad degenerativa Sistema nervosio central patología Sistema nervioso patología
Classification
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
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
13737829

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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