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Neuropathologic heterogeneity in HDDD1 : A familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and Progranulin mutation

Author
BEHRENS, Maria I1 2 ; MUKHERJEE, Odity1 3 ; CHAKRAVERTY, Sumi1 3 ; GOATE, Alison M1 3 ; MORRIS, John C1 4 7 ; CAIRNS, Nigel J1 4 ; TU, Pang-Hsien1 4 ; LISCIC, Rajka M1 5 ; TENENHOLZ GRINBERG, Lea1 4 6 ; CARTER, Deborah1 4 ; PAULSMEYER, Katherine1 4 ; TAYLOR-REINWALD, Lisa1 4 ; GITCHO, Michael1 7 ; NORTON, Joanne B1 3
[1] Alzheimer's Disease Research Center, Washington University School of Medicine, St Louis, MO, United States
[2] Departamento de Neurologia y Neurocirugia, Hospital Clínico Universidad de Chile and Clínica Alemana, Santiago, Chile
[3] Department of Psychiatry, Washington University School of Medicine, St Louis, MO, United States
[4] Departments of Pathology and Immunology, Washington University School of Medicine, St Louis, MO, United States
[5] Institute for Medical Research and Occupational Health, Zagreb, Croatia
[6] Department of Pathology, University of Sao Paulo Medical School, Sao Paulo, Brazil
[7] Department of Neurology, Washington University School of Medicine, St Louis, MO, United States
Source

Alzheimer disease and associated disorders. 2007, Vol 21, Num 1, pp 1-7, 7 p ; ref : 38 ref

CODEN
ADADE2
ISSN
0893-0341
Scientific domain
Neurology; Psychophysiology; Psychology, psychopathology, psychiatry
Publisher
Lippincott Williams & Wilkins, Hagerstown, MD
Publication country
United States
Document type
Article
Language
English
Author keyword
Alzheimer disease FTLD-U HDDD1 frontotemporal lobar degeneration progranulin mutation
Keyword (fr)
Diagnostic Dysphasie Dégénérescence Démence Alzheimer Démence Dépendance Etude cas Frontal Histopathologie Hétérogénéité Immunohistochimie Mutation Mémoire Structure neurofibrillaire Système nerveux pathologie Trouble cognition Trouble langage Trouble mémoire Trouble personnalité Ubiquitine Encéphale pathologie Maladie dégénérative Système nerveux central pathologie Trouble communication
Keyword (en)
Diagnosis Dysphasia Degeneration Alzheimer disease Dementia Dependence Case study Frontal Histopathology Heterogeneity Immunohistochemistry Mutation Memory Neurofibrillary tangle Nervous system diseases Cognitive disorder Language disorder Memory disorder Personality disorder Ubiquitin Cerebral disorder Degenerative disease Central nervous system disease Communication disorder
Keyword (es)
Diagnóstico Disfasia Degeneración Demencia Alzheimer Demencia Dependencia Estudio caso Frontal Histopatología Heterogeneidad Inmunohistoquímica Mutación Memoria Estructura neurofibrilar Sistema nervioso patología Trastorno cognitivo Trastorno lenguaje Trastorno memoria Trastorno personalidad Ubiquitina Encéfalo patología Enfermedad degenerativa Sistema nervosio central patología Trastorno comunicación
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B12 Cardiology. Vascular system / 002B12B Blood and lymphatic vessels / 002B12B01 Atherosclerosis (general aspects, experimental research)

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17A Nervous system (semeiology, syndromes) / 002B17A03 Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy

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
Cardiology. Circulatory system Neurology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
18604198

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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