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Serveur d'exploration sur les relations entre la France et l'Australie - Analysis (UK)

Index « Auteurs » - entrée « Alan Coulthard »
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Alan Cooper < Alan Coulthard < Alan Cowman  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 2.
Ident.Authors (with country if any)Title
002F63 (2007) Patrick F. Chinnery [Royaume-Uni] ; Douglas E. Crompton [Royaume-Uni] ; Daniel Birchall [Royaume-Uni] ; Margaret J. Jackson [Royaume-Uni] ; Alan Coulthard [Royaume-Uni, Australie] ; Anne Lombes [France] ; Niall Quinn [Royaume-Uni] ; Adrian Wills [Royaume-Uni] ; Nicholas Fletcher [Royaume-Uni] ; John P. Mottershead [Royaume-Uni] ; Paul Cooper [Royaume-Uni] ; Mark Kellett [Royaume-Uni] ; David Bates [Royaume-Uni] ; John Burn [Royaume-Uni]Clinical features and natural history of neuroferritinopathy caused by the FTLI 460InsA mutation
003043 (2006) Patrick F. Chinnery ; Douglas E. Crompton ; Daniel Birchall [Royaume-Uni] ; Margaret J. Jackson ; Alan Coulthard [Royaume-Uni, Australie] ; Anne Lombès [France] ; Niall Quinn [Royaume-Uni] ; Adrian Wills [Royaume-Uni] ; Nicholas Fletcher [Royaume-Uni] ; John P. Mottershead [Royaume-Uni] ; Paul Cooper [Royaume-Uni] ; Mark Kellett [Royaume-Uni] ; David Bates ; John BurnClinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation

List of associated KwdEn.i

Nombre de
documents		Descripteur
2Chorea
2Dystonia
2Ferritin
2Mutation
1Abnormal iron storage
1Ataxia
1Basal ganglia
1Brain imaging
1Brain iron stores
1Brisk tendon reflexes
1Case number
1Caudate nuclei
1Cerebellar signs
1Characteristic pattern
1Chinnery
1Clinical course
1Clinical features
1Clinical presentation
1Cognitive
1Cognitive impairment
1Common mutation
1Curtis
1Dentate nuclei
1Differential diagnosis
1Disease course
1Disease duration
1Disorder
1Dyskinesia
1Early case
1Early stages
1Ethnic origin
1Family history
1Ferritin light chain gene
1Fluency
1Focal dystonia
1Ftl1
1Ftl1 mutation
1Further cases
1Generalized dystonia
1Globi pallidi
1Globus pallidus
1Hereditary ferritinopathy
1High signal
1Idiopathic
1Idiopathic disease
1Idiopathic torsion dystonia
1Imaging
1Intermediate case
1Iron
1Iron deposition
1Late onset
1Mancuso
1Mineral deposition
1Mitochondrial
1Mitochondrial disease
1Mitochondrial disorders
1Movement disorder
1Movement disorders
1Muscle biopsy
1Natural history
1Nervous system diseases
1Neurodegenerative disease
1Neuroferritinopathy
1Neuroferritinopathy brain
1Neurol
1Neurol neurosurg psychiatry
1Orolingual dyskinesia speech
1Palatal tremor
1Pank2 deficiency
1Phenotype
1Phenotype bradykinesia table
1Psychiatric features
1Psychometry
1Range months
1Range years
1Reading frame
1Recessive choreoacanthocytosis
1Resonance imaging
1Respiratory chain
1Respiratory chain defects
1Same subjects
1Serum ferritin
1Serum ferritin levels
1Signal increase
1Signal loss
1Significant difference
1Skeletal muscle
1Spinocerebellar ataxia
1Substantia nigra
1Tremor
1Vast majority
1Verbal fluency
1Weighted images
1Wellcome trust

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