DÜRR (A.) < DÜRR (Alexandra) < DÜRRAFILLER (Nick)

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 23.
[0-20] [0 - 20][0 - 23][20-22][20-40]

Ident.	Authors (with country if any)	Title
000132 (2000)	Alexandra Dürr ; Christoph Lücking ; Alexis Brice	La maladie de Parkinson due aux mutations de la parkine
000197 (2001)	Magali Periquet ; Christoph B. Lücking ; Jenny R. Vaughan ; Vincenzo Bonifati ; Alexandra Dürr ; Giuseppe De Michele ; Martin W. Horstink ; Matt Farrer ; Sergei N. Illarioshkin ; Pierre Pollak ; Michel Borg ; Christine Brefel-Courbon ; Patrice Denefle ; Giuseppe Meco ; Thomas Gasser ; Monique M. B. Breteler ; Nick W. Wood ; Yves Agid ; Alexis Brice	Origin of the mutations in the parkin gene in Europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects
000277 (2002)	Enza Maria Valente ; Francesco Brancati ; Alessandro Ferraris ; Elizabeth A. Graham ; Mary B. Davis ; Monique M. B. Breteler ; Thomas Gasser ; Vincenzo Bonifati ; Anna Rita Bentivoglio ; Giuseppe De Michele ; Alexandra Dürr ; Pietro Cortelli ; Dietmar Wassilowsky ; Biswadjiet S. Harhangi ; Nina Rawal ; Viviana Caputo ; Alessandro Filla ; Giuseppe Meco ; Ben A. Oostra ; Alexis Brice ; Alberto Albanese ; Bruno Dallapiccola ; Nicholas W. Wood	PARK6-linked parkinsonism occurs in several European families
000369 (2002)	Andrew West ; Magali Periquet ; Sarah Lincoln ; Christoph B. Lücking ; David Nicholl ; Vincenzo Bonifati ; Nina Rawal ; Thomas Gasser ; Ebba Lohmann ; Jean-Francois Deleuze ; Demetrius Maraganore ; Allan Levey ; Nick Wood ; Alexandra Dürr ; John Hardy ; Alexis Brice ; Matt Farrer	Complex relationship between Parkin mutations and Parkinson disease
000450 (2002)	Nina Rawal ; Magali Periquet ; Alexandra Dürr ; Giuseppe De Michele ; Vincenzo Bonifati ; Helio A. Teive ; Salmo Raskin ; Joao Guimaraes ; Yves Agid ; Alexis Brice	Exclusion of the Nurr1 gene in autosomal recessive Parkinson's disease
000457 (2003)	Thomas Gasser ; Susan Bressman ; Alexandra Dürr ; Joseph Higgins ; Thomas Klockgether ; Richard H. Myers	Molecular diagnosis of inherited movement disorders. Movement disorders Society Task Force on Molecular Diagnosis
000516 (2003)	Stéphane Thobois ; Maria-Joao Ribeiro ; Ebba Lohmann ; Alexandra Dürr ; Pierre Pollak ; Olivier Rascol ; Stéphane Guillouet ; Elizabeth Chapoy ; Nicolas Costes ; Yves Agid ; Philippe Remy ; Alexis Brice ; Emmanuel Broussolle	Young-onset Parkinson disease with and without parkin gene mutations: A fluorodopa F 18 positron emission tomography study
000569 (2003)	Christoph-Burkhard Lücking ; Véronique Chesneau ; Ebba Lohmann ; Patrice Verpillat ; Cyprien Dulac ; Anne-Marie Bonnet ; Francesca Gasparini ; Yves Agid ; Alexandra Dürr ; Alexis Brice	Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease
000642 (2002)	Claire Borie ; Francesca Gasparini ; Patrice Verpillat ; Anne-Marie Bonnet ; Yves Agid ; Gilles Hetet ; Alexis Brice ; Alexandra Dürr ; Bernard Grandchamp	Association study between iron-related genes polymorphisms and Parkinson's disease
000762 (2005)	Maria Martinez ; Alexis Brice ; Jenny R. Vaughan ; Alexander Zimprich ; Monique M. B. Breteler ; Giuseppe Meco ; Alessandro Filla ; Matthew J. Fatter ; Christine Betard ; Andrew Singleton ; John Hardy ; Giuseppe De Michele ; Vincenzo Bonifati ; Ben A. Oostra ; Thomas Gasser ; Nick W. Wood ; Alexandra Dürr	Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease
000839 (2006)	Pablo Ibanez ; Suzanne Lesage ; Ebba Lohmann ; Stéphane Thobois ; Giuseppe De Michele ; Michel Borg ; Yves Agid ; Alexandra Dürr ; Alexis Brice	Mutational analysis of the PINK I gene in early-onset parkinsonism in Europe and North Africa
000906 (2006)	Anne-Louise Leutenegger ; Mustafa A. M. Salih ; Pablo Ibanez ; Maowia M. Mukhtar ; Suzanne Lesage ; All Arabi ; Ebba Lohmann ; Alexandra Dürr ; Ammar E. M. Ahmed ; Alexis Brice	Juvenile-onset parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1
000910 (2006)	Suzanne Lesage ; Alexandra Dürr ; Alexis Brice	LRRK2, gène majeur de la maladie de parkinson dans les pays du Maghreb
000960 (2007)	Michael Schüpbach ; Ebba Lohmann ; Mathieu Anheim ; Suzanne Lesage ; Virginie Czernecki ; Sadek Yaici ; Yulia Worbe ; Perrine Charles ; Marie-Laure Welter ; Pierre Pollak ; Alexandra Dürr ; Yves Agid ; Alexis Brice	Subthalamic nucleus stimulation is efficacious in patients with parkinsonism and LRRK2 mutations
000971 (2007)	Suzanne Lesage ; Sabine Janin ; Ebba Lohmann ; Anne-Louise Leutenegger ; Laurence Leclere ; Francois Viallet ; Pierre Pollak ; Franck Durif ; Stephane Thobois ; Valérie Layet ; Marie Vidailhet ; Yves Agid ; Alexandra Dürr ; Alexis Brice	LRRK2 exon 41 mutations in sporadic parkinson disease in europeans
000978 (2007)	Anne Grünewald ; Guido J. Breedveld ; Katja Lohmann-Hedrich ; Christan F. Rohe ; Inke R. König ; Johann Hagenah ; Nicola Vanacore ; Giuseppe Meco ; Angelo Antonini ; Stefano Goldwurm ; Suzanne Lesage ; Alexandra Dürr ; Ferdinand Binkofski ; Hartwig Siebner ; Alexander Münchau ; Alexis Brice ; Ben A. Oostra ; Christine Klein ; Vincenzo Bonifati	Biological effects of the PINK1 c.1366C>T mutation : implications in Parkinson disease pathogenesis
000A99 (2008)	Corinne Lautier ; Stefano Goldwurm ; Alexandra Dürr ; Barbara Giovannone ; William G. Tsiaras ; Gianni Pezzoli ; Alexis Brice ; Robert J. Smith	Mutations in the GIGYF2 (TNRC15) Gene at the PARK11 Locus in Familial Parkinson Disease
000B95 (2009)	Pablo Ibanez ; LESAGE ; Sabine Janin ; Ebba Lohmann ; Frank Durif ; Alain Destee ; Anne-Marie Bonnet ; Christine Brefel-Courbon ; Simon Heath ; Diana Zelenika ; Yves Agid ; Alexandra Dürr ; Alexis Brice	α-Synuclein Gene Rearrangements in Dominantly Inherited Parkinsonism : Frequency, Phenotype, and Mechanisms
000B96 (2008)	Agnès Camuzat ; Marc Romana ; Alexandra Dürr ; Josué Feingold ; Alexis Brice ; Merle Ruberg ; Annie Lannuzel	The PSP-Associated MAPT H1 Subhaplotype in Guadeloupean Atypical Parkinsonism
000D16 (2009)	Nadège Limousin ; Eric Konofal ; Elias Karroum ; Ebba Lohmann ; Ioannis Theodorou ; Alexandra Dürr ; Isabelle Amulf	Restless Legs Syndrome, Rapid Eye Movement Sleep Behavior Disorder, and Hypersomnia in Patients with Two Parkin Mutations
000D89 (2010)	Suzanne Lesage ; Etienne Patin ; Christel Condroyer ; Anne-Louise Leutenegger ; Ebba Lohmann ; Nir Giladi ; Anat Bar-Shira ; Soraya Belarbi ; Nassima Hecham ; Pierre Pollak ; Anne-Marie Ouvrard-Hernandez ; Soraya Bardien ; Jonathan Carr ; Traki Benhassine ; Hiroyuki Tomiyama ; Caroline Pirkevi ; Tarik Hamadouche ; Cécile Cazeneuve ; A. Nazli Basak ; Nobutaka Hattori ; Alexandra Dürr ; Meriem Tazir ; Avi Orr-Urtreger ; Lluis Quintana-Murci ; Alexis Brice	Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

---

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/ParkinsonFranceV1/Data/PascalFrancis/Merge

HfdIndexSelect -h $EXPLOR_AREA/Data/PascalFrancis/Merge/FA11s1.i -k "DÜRR (Alexandra)" 

HfdIndexSelect -h $EXPLOR_AREA/Data/PascalFrancis/Merge/FA11s1.i  \
                -Sk "DÜRR (Alexandra)" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/PascalFrancis/Merge/biblio.hfd 

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    ParkinsonFranceV1
   |flux=    PascalFrancis
   |étape=   Merge
   |type=    indexItem
   |index=    FA11s1.i
   |clé=    DÜRR (Alexandra)
}}

---

This area was generated with Dilib version V0.6.29. Data generation: Wed May 17 19:46:39 2017. Site generation: Mon Mar 4 15:48:15 2024