Age Factors < Age of Onset < Aged

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 251.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000078 (1999)	O. Joost [États-Unis] ; C A Taylor ; C A Thomas ; L A Cupples ; M H Saint-Hilaire ; R G Feldman ; C T Baldwin ; R H Myers	Absence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's disease.
000091 (1999)	C. Kamm [Allemagne] ; E. Castelon-Konkiewitz ; M. Naumann ; F. Heinen ; M. Brack ; A. Nebe ; A. Ceballos-Baumann ; T. Gasser	GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany.
000094 (1999)	S. Frucht [États-Unis] ; S. Fahn	Paroxysmal kinesigenic dyskinesia in infancy.
000332 (2000)	J P Larsen [Norvège] ; K. Karlsen ; E. Tandberg	Clinical problems in non-fluctuating patients with Parkinson's disease: a community-based study.
000349 (2000)	L. Vercueil [France] ; A. Hammouti ; M L Andriantseheno ; M. Mohr ; C. Tranchant ; P. Maquet ; C. Marescaux ; F. Sellal	Pallido-Luysio-Nigral atrophy revealed by rapidly progressive hemidystonia: a clinical, radiologic, functional, and neuropathologic study.
000350 (2000)	A. Münchau [Royaume-Uni] ; E M Valente ; M B Davis ; V. Stinton ; N W Wood ; N P Quinn ; K P Bhatia	A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia.
000366 (2000)	S N Illarioshkin [Russie] ; I A Ivanova-Smolenskaya ; R A Rahmonov ; E D Markova ; G. Stevanin ; A. Brice	Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan.
000375 (2000)	M. Farrer [États-Unis] ; T. Destée ; E. Becquet ; F. Wavrant-De Vrièze ; V. Mouroux ; F. Richard ; L. Defebvre ; S. Lincoln ; J. Hardy ; P. Amouyel ; M C Chartier-Harlin	Linkage exclusion in French families with probable Parkinson' s disease.
000391 (2000)	E Y Uc [États-Unis] ; D A Wenger ; Joseph Jankovic [États-Unis]	Niemann-Pick disease type C: two cases and an update.
000402 (2000)	A. Filla [Italie] ; G. De Michele ; G. Coppola ; A. Federico ; G. Vita ; A. Toscano ; A. Uncini ; P. Pisanelli ; P. Barone ; V. Scarano ; A. Perretti ; L. Santoro ; A. Monticelli ; F. Cavalcanti ; G. Caruso ; S. Cocozza	Accuracy of clinical diagnostic criteria for Friedreich's ataxia.
000424 (2001)	H. Ujike [Japon] ; M. Yamamoto ; A. Kanzaki ; K. Okumura ; M. Takaki ; S. Kuroda	Prevalence of homozygous deletions of the parkin gene in a cohort of patients with sporadic and familial Parkinson's disease.
000425 (2001)	J. Shahed [États-Unis] ; Joseph Jankovic [États-Unis]	Re-emergence of childhood stuttering in Parkinson's disease: a hypothesis.
000502 (2001)	J E Ahlskog [États-Unis] ; M D Muenter	Frequency of levodopa-related dyskinesias and motor fluctuations as estimated from the cumulative literature.
000508 (2001)	P C Jedynak [France] ; C. Tranchant ; D Z De Beyl	Prospective clinical study of writer's cramp.
000515 (2001)	M H Saint-Hilaire [États-Unis] ; J M Saint-Hilaire	Jumping Frenchmen of Maine.
000594 (2001)	P J Hand [Australie] ; R J Gardner ; M A Knight ; S M Forrest ; E. Storey	Clinical features of a large Australian pedigree with episodic ataxia type 1.
000606 (2001)	A R Bentivoglio [Italie] ; P. Cortelli ; E M Valente ; T. Ialongo ; A. Ferraris ; A. Elia ; P. Montagna ; A. Albanese	Phenotypic characterisation of autosomal recessive PARK6-linked parkinsonism in three unrelated Italian families.
000607 (2001)	S. Bostantjopoulou [Grèce] ; Z. Katsarou ; A. Papadimitriou ; V. Veletza ; G. Hatzigeorgiou ; A. Lees	Clinical features of parkinsonian patients with the alpha-synuclein (G209A) mutation.
000627 (2001)	B A Racette [États-Unis] ; A. Perry ; G. D'Avossa ; J S Perlmutter	Late-onset neurodegeneration with brain iron accumulation type 1: expanding the clinical spectrum.
000628 (2001)	D O Mcdaniel [États-Unis] ; B. Keats ; V V Vedanarayanan ; S H Subramony	Sequence variation in GAA repeat expansions may cause differential phenotype display in Friedreich's ataxia.
000838 (2002)	Jian Wang [République populaire de Chine] ; Chun-Ying Zhao ; Yan-Mei Si ; Zhuo-Lin Liu ; Biao Chen ; Long Yu	ACT and UCH-L1 polymorphisms in Parkinson's disease and age of onset.

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