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RÉTROSPECTIVE, PROSPECTIVE, OU PRÉDICTIVE Consultation de génétique de l'adulte: le risque d'une maladie génétique = Genetic counseling for adults: the risk of late-onset inherited diseasesDÜRR, Alexandra; FEINGOLD, Josué.La Revue du praticien (Paris). 2011, Vol 61, Num 4, pp 535-538, issn 0035-2640, 4 p.Article

LRRK2, gène majeur de la maladie de parkinson dans les pays du Maghreb = LRRK2 is a major gene in North Zfrican parkinsonismLESAGE, Suzanne; DÜRR, Alexandra; BRICE, Alexis et al.MS. Médecine sciences. 2006, Vol 22, Num 5, pp 470-471, issn 0767-0974, 2 p.Article

La maladie de Parkinson due aux mutations de la parkine = Parkin gene mutations and Parkinson's diseaseDÜRR, Alexandra; LÜCKING, Christoph; BRICE, Alexis et al.MS. Médecine sciences. 2000, Vol 16, Num 10, pp 1112-1115, issn 0767-0974Article

Les tests présymptomatiques en neurogénétique = Predictive testing : presymptomatic diagnosis in neurogenetic disordersDüRR, Alexandra; GARGIULO, Marcela; FEINGOLD, Josué et al.MS. Médecine sciences. 2005, Vol 21, Num 11, pp 934-939, issn 0767-0974, 6 p.Article

C9orf72 repeat expansions are a rare genetic cause of parkinsonismLESAGE, Suzanne; LE BER, Isabelle; ROULEAU, Guy A et al.Brain. 2013, Vol 136, pp 385-391, issn 0006-8950, 7 p., 2Article

Parkin mutations are frequent in patients with isolated early-onset parkinsonismPERIQUET, Magali; LATOUCHE, Morwena; BARONE, Paolo et al.Brain. 2003, Vol 126, pp 1271-1278, issn 0006-8950, 8 p., 6Article

CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxiaFUJIGASAKI, Hiroto; MARTIN, Jean-Jacques; DE DEYN, Peter Paul et al.Brain. 2001, Vol 124, pp 1939-1947, issn 0006-8950, 10Article

Restless Legs Syndrome, Rapid Eye Movement Sleep Behavior Disorder, and Hypersomnia in Patients with Two Parkin MutationsLIMOUSIN, Nadège; KONOFAL, Eric; KARROUM, Elias et al.Movement disorders. 2009, Vol 24, Num 13, pp 1970-1976, issn 0885-3185, 7 p.Article

Molecular diagnosis of inherited movement disorders. Movement disorders Society Task Force on Molecular DiagnosisGASSER, Thomas; BRESSMAN, Susan; DÜRR, Alexandra et al.Movement disorders. 2003, Vol 18, Num 1, pp 3-18, issn 0885-3185, 16 p.Article

TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairmentDELPLANQUE, Jérôme; DEVOS, David; BUEE, Luc et al.Brain. 2014, Vol 137, pp 2657-2663, issn 0006-8950, 7 p., 10Article

PRRT2 mutations: A major cause of paroxysmal kinesigenic dyskinesia in the European populationMENERET, Aurélie; GRABLI, David; ANHEIM, Mathieu et al.Neurology. 2012, Vol 79, Num 2, pp 170-174, issn 0028-3878, 5 p.Article

LINGO1 Polymorphisms Are Associated with Essential Tremor in EuropeansTHIER, Sandra; LORENZ, Delia; NOTHNAGEL, Michael et al.Movement disorders. 2010, Vol 25, Num 6, pp 717-723, issn 0885-3185, 7 p.Article

Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patientsLORENZ, Delia; KLEBE, Stephan; BRICE, Alexis et al.European journal of human genetics. 2009, Vol 17, Num 6, pp 766-773, issn 1018-4813, 8 p.Article

Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patientsLE BER, Isabelle; BOUSLAM, Naima; AGID, Yves et al.Brain. 2004, Vol 127, pp 759-767, issn 0006-8950, 9 p., 4Article

Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2pSTEVANIN, Giovanni; BOUSLAM, Naima; THOBOIS, Stéphane et al.Annals of neurology. 2004, Vol 55, Num 1, pp 97-104, issn 0364-5134, 8 p.Article

Atlastinl mutations are frequent in young-onset autosomal dominant spastic paraplegiaDÜRR, Alexandra; CAMUZAT, Agnès; RUBERG, Merle et al.Archives of neurology (Chicago). 2004, Vol 61, Num 12, pp 1867-1872, issn 0003-9942, 6 p.Article

Young-onset Parkinson disease with and without parkin gene mutations: A fluorodopa F 18 positron emission tomography studyTHOBOIS, Stéphane; RIBEIRO, Maria-Joao; REMY, Philippe et al.Archives of neurology (Chicago). 2003, Vol 60, Num 5, pp 713-718, issn 0003-9942, 6 p.Article

Exclusion of the Nurr1 gene in autosomal recessive Parkinson's diseaseRAWAL, Nina; PERIQUET, Magali; DÜRR, Alexandra et al.Journal of neurology. 2002, Vol 249, Num 8, pp 1127-1129, issn 0340-5354, 3 p.Article

Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6REETZ, Kathrin; COSTA, Ana S; GRISOLI, Marina et al.Brain. 2013, Vol 136, pp 905-917, issn 0006-8950, 13 p., 3Article

Rating disease progression of Friedreich's ataxia by the International Cooperative Ataxia Rating Scale: analysis of a 603-patient databaseMETZ, Günther; COPPARD, Nicholas; MEIER, Thomas et al.Brain. 2013, Vol 136, pp 259-268, issn 0006-8950, 10 p., 1Article

Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's diseaseTOUT, Julie C; JONES, Rebecca; HART, Ellen P et al.Journal of neurology, neurosurgery and psychiatry. 2012, Vol 83, Num 7, pp 687-694, issn 0022-3050, 8 p.Article

Self-Rated Health Status in Spinocerebellar Ataxia—Results from a European Multiceriter StudySCHMITZ-HÜBSCH, Tanja; COUDERT, Mathieu; RIBAI, Pascale et al.Movement disorders. 2010, Vol 25, Num 5, pp 587-595, issn 0885-3185, 9 p.Article

Asian origin for the worldwide-spread mutational event in machado-joseph diseaseMARTINS, Sandra; CALAFELL, Francesc; SOONG, Bing-Wen et al.Archives of neurology (Chicago). 2007, Vol 64, Num 10, pp 1502-1508, issn 0003-9942, 7 p.Article

Spectrin mutations cause spinocerebellar ataxia type 5IKEDA, Yoshio; DICK, Katherine A; BRENT CLARK, H et al.Nature genetics. 2006, Vol 38, Num 2, pp 184-190, issn 1061-4036, 7 p.Article

Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3AABEL, Annette; FONKNECHTEN, Nuria; HAZAN, Jamilé et al.Neurogenetics (Oxford. Print). 2004, Vol 5, Num 4, pp 239-243, issn 1364-6745, 5 p.Article

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