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

Index « Auteurs » - entrée « B. Ghetti »
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B. G. Landwehrmeyer < B. Ghetti < B. Giebels  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 4.
Ident.Authors (with country if any)Title
000659 (2006) A.-M. Shiarli [Royaume-Uni] ; R. Jennings [Royaume-Uni] ; J. Shi [Royaume-Uni, République populaire de Chine] ; K. Bailey [Royaume-Uni] ; Y. Davidson [Royaume-Uni] ; J. Tian [Royaume-Uni, République populaire de Chine] ; E. H. Bigio [États-Unis] ; B. Ghetti [États-Unis] ; J. R. Murrell [États-Unis] ; M. B. Delisle [France] ; S. Mirra [États-Unis] ; B. Crain [États-Unis] ; P. Zolo [Italie] ; K. Arima [Japon] ; E. Iseki [Japon] ; S. Murayama [Japon] ; H. Kretzschmar ; M. Neumann ; C. Lippa ; G. Halliday ; J. Mackenzie ; N. Khan ; R. Ravid ; D. Dickson ; Z. Wszolek ; T. Iwatsubo ; S. M. Pickering-Brown [Royaume-Uni] ; D. M. A. Mann [Royaume-Uni]Comparison of extent of tau pathology in patients with frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease
000768 (2002) Y. Tsuboi [États-Unis] ; M. Baker ; M L Hutton ; R J Uitti ; O. Rascol ; M-B Delisle ; X. Soulages ; J R Murrell ; B. Ghetti ; M. Yasuda ; O. Komure ; S. Kuno ; K. Arima ; N. Sunohara ; T. Kobayashi ; Y. Mizuno ; Z K WszolekClinical and genetic studies of families with the tau N279K mutation (FTDP-17).
000838 (1999) S S Mirra [États-Unis] ; J R Murrell ; M. Gearing ; M G Spillantini ; M. Goedert ; R A Crowther ; A I Levey ; R. Jones ; J. Green ; J M Shoffner ; B H Wainer ; M L Schmidt ; J Q Trojanowski ; B. GhettiTau pathology in a family with dementia and a P301L mutation in tau.
000916 (1995) L. C. Triarhou [États-Unis] ; C. Solà [Espagne] ; G. Mengod [Espagne] ; F. J. Garcia-Ladona [France] ; B. Landwehrmeyer [Suisse] ; B. Ghetti [États-Unis] ; J. M. Palacios [Espagne]Ventral mesencephalic grafts in the neostriatum of the weaver mutant mouse: Structural molecule and receptor studies

List of associated KwdEn.i

Nombre de
documents		Descripteur
2Dementia (genetics)
2France
2Humans
2Male
2Parkinson Disease (genetics)
2tau Proteins (genetics)
1Adult
1Alzheimer disease
1Anatomic pathology
1Antiparkinson Agents (therapeutic use)
1Atrophy
1Blotting, Western
1Canada
1Chromosome 17
1Chromosomes, Human, Pair 17 (genetics)
1Comparative study
1DNA (genetics)
1DNA Mutational Analysis
1DNA Probes
1Degeneration
1Dementia (pathology)
1Dementia (physiopathology)
1Early
1Epitopes (genetics)
1Family Health
1Female
1Founder Effect
1Frontal Lobe
1Frontal Lobe (pathology)
1Frontotemporal dementia
1Gene
1Human
1Japan
1Levodopa (therapeutic use)
1Microsatellite Repeats (genetics)
1Microscopy, Electron
1Microtubule associated protein
1Middle Aged
1Molecular Biology
1Mutation (genetics)
1Nerve Degeneration (genetics)
1Nervous system diseases
1Neurofibrillary Tangles (chemistry)
1Neurofibrillary Tangles (ultrastructure)
1Neurofibrillary tangle
1Neurons (chemistry)
1Neurons (pathology)
1Parietal Lobe (pathology)
1Parkinson Disease (pathology)
1Parkinson Disease (physiopathology)
1Parkinson disease
1Parkinsonism
1Pedigree
1Penetrance
1Pick body
1Point Mutation
1Polymerase Chain Reaction
1Restriction Mapping
1Solubility
1Tau protein
1Temporal Lobe
1Temporal Lobe (pathology)
1United States
1tau Proteins (analysis)

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