Christine Höft < Christine Klein < Christine L. Jones

Facettes :

List of bibliographic references indexed by Christine Klein

Number of relevant bibliographic references: 24.
[20-40] [0 - 20][0 - 24]

Ident.	Authors (with country if any)	Title
001652 (2004)	Katja Hedrich [Allemagne] ; Cordula Eskelson [Allemagne] ; Beth Wilmot [États-Unis] ; Karen Marder [États-Unis] ; Juliette Harris [États-Unis] ; Jennifer Garrels [Allemagne] ; Helen Meija-Santana [États-Unis] ; Peter Vieregge [Allemagne] ; Helfried Jacobs [Allemagne] ; Susan B. Bressman [États-Unis] ; Anthony E. Lang [Canada] ; Martin Kann [Allemagne] ; Giovanni Abbruzzese [Italie] ; Paolo Martinelli [Italie] ; Eberhard Schwinger [Allemagne] ; Laurie J. Ozelius [États-Unis] ; Peter P. Pramstaller [Italie, États-Unis] ; Christine Klein [Allemagne] ; Patricia Kramer [États-Unis]	Distribution, type, and origin of Parkin mutations: Review and case studies
001658 (2004)	Ana Djarmati [Allemagne, Serbie] ; Katja Hedrich [Allemagne] ; Marina Svetel [Serbie] ; Nora Sch Fer [Allemagne] ; Vladislava Juric [Serbie] ; Slobodanka Vukosavic [Serbie] ; Robert Hering [Serbie] ; Olaf Riess [Allemagne] ; Stanka Romac [Serbie] ; Christine Klein [Allemagne] ; Vladimir Kostic [Serbie]	Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early‐onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients
001B91 (2000)	Christine Klein [États-Unis, Allemagne] ; Peter P. Pramstaller [Italie] ; Bernhard Kis [Allemagne, Italie] ; Curtis C. Page [États-Unis] ; Martin Kann [États-Unis] ; Joanne Leung [États-Unis] ; Heather Woodward [États-Unis] ; Claudio C. Castellan [Italie] ; Monika Scherer [Italie] ; Peter Vieregge [Allemagne] ; Xandra O. Breakefield [États-Unis] ; Patricia L. Kramer [États-Unis] ; Laurie J. Ozelius [États-Unis]	Parkin deletions in a family with adult‐onset, tremor‐dominant parkinsonism: Expanding the phenotype
001E62 (1998)	Christine Klein [États-Unis] ; Laurie J. Ozelius [États-Unis] ; Johann Hagenah [Allemagne] ; Xandra O. Breakefield [États-Unis] ; Neil J. Risch ; Peter Vieregge [Allemagne]	Search for a Founder Mutation in Idiopathic Focal Dystonia from Northern Germany

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List of associated KwdEn.i

Nombre de documents	Descripteur
9	Parkinson's disease
2	genetics
2	recurrent mutations
1	ATP13A2 mutations
1	CAG repeat
1	Chromosome 18p
1	DJ1
1	DJ1, PARK7
1	DNA methylation
1	DRD3 Ser9Gly
1	EOPD
1	Early‐onset Parkinson disease
1	Focal dystonia
1	Gaucher disease
1	German Competence Network on Parkinson's disease
1	Hardy-Weinberg analysis
1	Huntington's disease
1	LINGO1
1	LRRK2
1	Linkage disequilibrium
1	PARK
1	PARK7
1	PINK1 gene
1	Parkin
1	Parkin, PARK2
1	Parkin, Parkinson's disease
1	Parkinson
1	Parkinson disease
1	Parkinson disease, autosomal recessive, early onset
1	Serbia
1	association study
1	break point analysis
1	camptocormia
1	chip
1	classification
1	color discrimination
1	compensation
1	crystallization
1	data protection
1	distribution
1	dopa‐responsive dystonia
1	dyskinesia
1	dystonia
1	early‐onset Parkinson's disease
1	exon rearrangements
1	functional imaging
1	functional magnetic resonance imaging
1	gene bank
1	genetic epidemiology
1	genetic testing
1	genotyping array
1	glucocerebrosidase mutations transcranial sonography
1	head drop syndrome
1	idiopathic basal ganglia calcification
1	juvenile Parkinsonism
1	lenticular nucleus
1	levodopa
1	linkage analysis
1	linkage disequilibrium
1	minimyoclonus
1	mitochondria
1	monogenic parkinsonism
1	motor complications
1	motor cortex
1	multiplex ligation‐dependent probe amplification
1	mutation
1	myoclonus‐dystonia
1	myopathy
1	olfaction
1	onset age
1	origin
1	parkin gene
1	parkinsonism
1	phenocopy
1	presymptomatic parkinsonism
1	protein‐surplus myopathy
1	remote data entry system
1	saccadic pursuit
1	sense of smell
1	standardized documentation
1	transcranial sonography

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