K. J. Friston < K. Jellinger < K. Joh-O

Facettes :

List of bibliographic references indexed by K. Jellinger

Number of relevant bibliographic references: 9.

Ident.	Authors (with country if any)	Title
001C49 (2000)	C. Scherfler [Autriche] ; Z. Puschban [Autriche] ; I. Ghorayeb [France] ; G. P Goebel [Autriche] ; F. Tison [France] ; K. Jellinger [Autriche] ; Werner Poewe [Autriche] ; G. K Wenning [Autriche]	Complex motor disturbances in a sequential double lesion rat model of striatonigral degeneration (multiple system atrophy)
002767 (1990)	P. Fischer [Autriche] ; G. Gatterer [Autriche] ; M. Simanyi [Autriche] ; K. Jellinger [Autriche] ; A. Marterer [Autriche] ; K. Danielczyk [Autriche] ; W. Danielczyk [Autriche]	Memory deficits in advanced Parkinson's disease
002783 (1990)	K. Jellinger ; W. Danielczyk ; P. Fischer ; E. Gabriel	Clinicopathological analysis of dementia disorders in the elderly
002787 (1990)	K. Jellinger [Autriche] ; W. Paulus [Autriche] ; I. Grundke-Iqbal [États-Unis] ; P. Riederer [Allemagne] ; H. Youdim [Israël]	Brain iron and ferritin in Parkinson's and Alzheimer's diseases
002A84 (1983)	P. Riederer [Autriche] ; K. Jellinger [Autriche]	Neurochemical insights into monoamine oxidase inhibitors, with special reference to deprenyl (selegiline)
002B62 (1980)	K. Jellinger ; H. Flament ; P. Riederer ; H. Schmid ; L. Ambrozi	Levodopa in the treatment of (PRE) senile dementia
002C82 (1973)	H. Bernheimer ; W. Birkmayer ; O. Hornykiewicz ; K. Jellinger ; F. Seitelberger	Brain dopamine and the syndromes of Parkinson and Huntington Clinical, morphological and neurochemical correlations
002C93 (1972)	K. Jellinger [Autriche] ; E. Neumayer [Autriche]	Unusual late-onset type of Hallervorden-Spatz disease
002D33 (1968)	K. Jellinger [Autriche] ; W. Danielczyk [Autriche]	„Striato-nigrale Degeneration”

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List of associated KwdEn.i

Nombre de documents	Descripteur
1	6-OHDA, 6-hydroxydopamine
1	6-hydroxydopamine
1	AChE, acetylcholinesterase
1	Alzheimer disease
1	Clinicopathological correlations
1	DAB, diaminobenzidine tetrahydrochloride
1	Dementia
1	GCI, glial cytoplasmic inclusion
1	GFAP, glial fibrillary acidic protein
1	HD, Huntington’s disease
1	HE, hematoxylin–eosin
1	MFB, medial forebrain bundle
1	MSA, multiple system atrophy
1	MSA-P, MSA-Parkinson subtype
1	Mixed type of dementia
1	PBS, phosphate-buffered saline
1	PD, Parkinson’s disease
1	Parkinson's disease
1	QA, quinolinic acid
1	SND, striatonigral degeneration
1	SNc, substantia nigra pars compacta
1	TH, tyrosine hydroxylase
1	Vascular dementia
1	balance test
1	deprenyl (selegiline)
1	glia
1	monoamine oxidase
1	neuroprotection
1	quinolinic acid
1	staircase test
1	stepping test

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