Alexandra Durr < Alexandra Dürr < Alexandra Furmston

Facettes :

List of bibliographic references indexed by Alexandra Dürr

Number of relevant bibliographic references: 4.

Ident.	Authors (with country if any)	Title
000967 (2009)	Nadège Limousin [France] ; Eric Konofal [France] ; Elias Karroum [France] ; Ebba Lohmann [France] ; Ioannis Theodorou [France] ; Alexandra Dürr [France] ; Isabelle Arnulf [France]	Restless legs syndrome, rapid eye movement sleep behavior disorder, and hypersomnia in patients with two parkin mutations
001083 (2007)	Suzanne Lesage [France] ; Periquet Magali [France] ; Ebba Lohmann [France] ; Lucette Lacomblez [France] ; Helio Teive [Brésil] ; Sabine Janin [France] ; Pierre-Yves Cousin [France] ; Alexandra Dürr [France] ; Alexis Brice [France]	Deletion of the parkin and PACRG gene promoter in early‐onset parkinsonism
001921 (2002)	Andrew West [États-Unis] ; Magali Periquet [France] ; Sarah Lincoln [États-Unis] ; Christoph B. Lücking [France, Allemagne] ; David Nicholl [Royaume-Uni] ; Vincenzo Bonifati ; Nina Rawal [France] ; Thomas Gasser [Allemagne] ; Ebba Lohmann [France] ; Jean-François Deleuze [France] ; Demetrius Maraganore [États-Unis] ; Allan Levey [Géorgie (pays)] ; Nick Wood [Royaume-Uni] ; Alexandra Dürr [France] ; John Hardy [États-Unis] ; Alexis Brice [France] ; Matt Farrer [États-Unis]	Complex relationship between Parkin mutations and Parkinson disease
001F21 (1998)	Johann Tassin ; Alexandra Dürr ; Thomas De Broucker [France] ; Nacer Abbas ; Vincenzo Bonifati ; Giuseppe De Michele ; Anne-Marie Bonnet ; Emmanuel Broussolle ; Pierre Pollak [France] ; Marie Vidailhet ; Michele De Mari ; Roberto Marconi [Italie] ; Soraya Medjbeur ; Allessandro Filla ; Giuseppe Meco ; Yves Agid [France] ; Alexis Brice [France]	Chromosome 6–Linked Autosomal Recessive Early-Onset Parkinsonism: Linkage in European and Algerian Families, Extension of the Clinical Spectrum, and Evidence of a Small Homozygous Deletion in One Family

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List of associated KwdEn.i

Nombre de documents	Descripteur
3	Parkinson disease
1	Autosomal recessive
1	Chromosome 6
1	Deletion
1	EOPD, early‐onset parkinsonism
1	Juvenile onset
1	Linkage
1	Parkin
1	Parkinson's disease
1	REM sleep behavior disorder
1	SOD2
1	haploinsufficiency
1	hypersomnia
1	inborn genetic diseases
1	neurodegeneration
1	parkin coregulated gene, PACRG
1	parkin, PARK2
1	promoter
1	restless legs syndrome

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