Frameshift Mutation < France < Free Radical Scavengers

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List of bibliographic references

Number of relevant bibliographic references: 140.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000006 (1999)	F. Boller [France] ; A. Ganansia-Ganem ; F. Lebert ; F. Pasquier	Neuropsychiatric afflictions of modern French presidents: Marechal Henri-Philippe Petain and Paul Deschanel.
000009 (1999)	N. Sabbagh [France] ; A. Brice ; D. Marez ; A. Dürr ; M. Legrand ; J M Lo Guidice ; A. Destée ; Yves Agid [France] ; F. Broly	CYP2D6 polymorphism and Parkinson's disease susceptibility.
000013 (1998)		Ropinirole: new preparation. Wait for more convincing data.
000017 (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. Ghetti	Tau pathology in a family with dementia and a P301L mutation in tau.
000025 (1999)	W J Holstein	Rewiring the brain. How a bright idea became an innovative medical device.
000054 (1999)	B S Harhangi [Pays-Bas] ; M J Farrer ; S. Lincoln ; V. Bonifati ; G. Meco ; G. De Michele ; A. Brice ; A. Dürr ; M. Martinez ; T. Gasser ; B. Bereznai ; J R Vaughan ; N W Wood ; J. Hardy ; B A Oostra ; M M Breteler	The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease.
000076 (1999)	C. Lepen [France] ; S. Wait ; F. Moutard-Martin ; M. Dujardin ; M. Ziégler	Cost of illness and disease severity in a cohort of French patients with Parkinson's disease.
000099 (????)		[Parkinson disease].
000100 (2000)	P. Haggard [Royaume-Uni] ; S. Rodgers	The movement disorder of Nicolas Poussin (1594-1665) [historical article].
000153 (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.
000191 (2001)	J L Montastruc [France] ; K. Desboeuf ; M. Lapeyre-Mestre ; J M Senard ; O. Rascol ; C. Brefel-Courbon	Long-term mortality results of the randomized controlled study comparing bromocriptine to which levodopa was later added with levodopa alone in previously untreated patients with Parkinson's disease.
000192 (2001)	C G Goetz [États-Unis] ; T A Chmura ; D J Lanska	Seminal figures in the history of movement disorders: Sydenham, Parkinson, and Charcot: Part 6 of the MDS-sponsored history of Movement Disorders exhibit, Barcelona, June 2000.
000197 (2001)	F. Maurel [France] ; H. Lilliu ; C. Le Pen	[Social and economic cost of L-Dopa-induced dyskinesias in patients with Parkinson's disease].
000206 (2001)	M. Peschanski	[10 years of substitution therapy for neurodegenerative diseases using fetal neuron grafts: a positive outcome but with questions for the future].
000215 (2001)	C. Levecque [France] ; A. Destée ; V. Mouroux ; E. Becquet ; L. Defebvre ; P. Amouyel ; M C Chartier-Harlin	No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease.
000242 (2002)	M. Bailbé ; S. Karolewicz ; J Ph Neau ; P. Dumas ; R. Gil	[Hallucinations, delusions, and nocturnal events in 152 Parkinson's patients: a regional survey].
000244 (2002)		Clozapine: new preparation. A last resort for parkinsonian patients with psychosis.
000269 (2002)	André Parent [Canada] ; Martin Parent ; Véronique Leroux-Hugon	Jules Bernard Luys: a singular figure of 19th century neurology.
000270 (2002)		Selegiline: a second look. Six years later: too risky in Parkinson's disease.
000296 (2002)	François Tison [France] ; Farid Yekhlef ; Eric Balestre ; Virginie Chrysostome ; Niall Quinn ; Gregor K. Wenning ; Werner Poewe [Autriche]	Application of the International Cooperative Ataxia Scale rating in multiple system atrophy.
000297 (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 Wszolek	Clinical and genetic studies of families with the tau N279K mutation (FTDP-17).

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