nov < novel < novelty

Facettes :

List of bibliographic references indexed by novel

Number of relevant bibliographic references: 133.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000011 (2015)	Roberto Erro [Italie]	VPS35 and EIF4G1 interactions and novel candidate genes for PD: from genes to pathways and back.
000085 (2015)	Michael Zech [Allemagne] ; Florian Castrop [Allemagne] ; Bernhard Haslinger [Allemagne] ; Juliane Winkelmann [Allemagne]	Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystonia.
000139 (2015)	Werner Poewe [Autriche] ; Angelo Antonini	Novel formulations and modes of delivery of levodopa.
000140 (2015)	Patricia De Carvalho Aguiar [Brésil] ; Vanderci Borges [Brésil] ; Henrique Ballalai Ferraz [Brésil] ; Laurie Jean Ozelius [États-Unis]	Novel compound heterozygous mutations in PRKRA cause pure dystonia.
000141 (2015)	Mafalda Raposo [Portugal] ; Conceição Bettencourt [Royaume-Uni] ; Patrícia Maciel [Portugal] ; Fuying Gao [États-Unis] ; Amanda Ramos [Portugal] ; Nadiya Kazachkova [Portugal] ; João Vasconcelos [Portugal] ; Teresa Kay [Portugal] ; Ana João Rodrigues [Portugal] ; Bruno Bettencourt [Portugal] ; Jácome Bruges-Armas [Portugal] ; Daniel Geschwind [États-Unis] ; Giovanni Coppola [États-Unis] ; Manuela Lima [Portugal]	Novel candidate blood-based transcriptional biomarkers of Machado-Joseph disease.
000175 (2015)	Marialuisa Quadri [Pays-Bas] ; Mahesh Kamate [Inde] ; Suvasini Sharma [Inde] ; Simone Olgiati [Pays-Bas] ; Josja Graafland [Pays-Bas] ; Guido J. Breedveld [Pays-Bas] ; Indu Kori [Inde] ; Virupaxi Hattiholi [Inde] ; Puneet Jain [Inde] ; Satinder Aneja [Inde] ; Atin Kumar [Inde] ; Parveen Gulati [Inde] ; Medha Goel [Inde] ; Bibek Talukdar [Inde] ; Vincenzo Bonifati [Pays-Bas]	Manganese transport disorder: novel SLC30A10 mutations and early phenotypes.
000177 (2015)	Uwe Walter [Allemagne] ; Jan-Uwe Müller [Allemagne] ; Johannes Rösche [Allemagne] ; Michael Kirsch [Allemagne] ; Annette Grossmann [Allemagne] ; Reiner Benecke [Allemagne] ; Matthias Wittstock [Allemagne] ; Alexander Wolters [Allemagne]	Magnetic resonance-transcranial ultrasound fusion imaging: A novel tool for brain electrode location.
000339 (2015)	Kishore Raj Kumar [Australie] ; Victor S C. Fung [Australie]	ADCY5 identified as a novel cause of benign hereditary chorea.
000346 (2015)	Samantha Slotnick [États-Unis] ; Yin Ding [États-Unis] ; Sofya Glazman [États-Unis] ; Mary Durbin [États-Unis] ; Shahnaz Miri [États-Unis] ; Ivan Selesnick [États-Unis] ; Jerome Sherman [États-Unis] ; Ivan Bodis-Wollner [États-Unis]	A novel retinal biomarker for Parkinson's disease: Quantifying the foveal pit with optical coherence tomography.
000353 (2015)	Diane Doummar [France] ; Cyril Mignot [France] ; Emmanuelle Apartis [France] ; Laurent Villard [France] ; Diana Rodriguez [France] ; Sandra Chantot-Bastauraud [France] ; Lydie Burglen [France]	A Novel Homozygous TBC1D24 Mutation Causing Multifocal Myoclonus With Cerebellar Involvement.
000354 (2015)	Janel O. Johnson [Royaume-Uni] ; Giovanni Stevanin ; Joyce Van De Leemput ; Dena G. Hernandez ; Sampath Arepalli ; Sylvie Forlani ; Reza Zonozi ; J Raphael Gibbs ; Alexis Brice ; Alexandra Durr ; Andrew B. Singleton	A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome.
000427 (2014)	Sheila M. Fleming [États-Unis] ; Alberto J. Espay	Ribosomal s15: A novel therapeutic target for Parkinson's disease.
000493 (2014)	Naomi P. Visanji [Canada]	Novel transgenic technology reveals several molecular adaptations and potential therapeutic targets in the direct pathway in levodopa-induced dyskinesia.
000494 (2014)	Geetanjali S. Rathore [États-Unis] ; Christian P. Schaaf ; Amber J. Stocco	Novel mutation of the WDR45 gene causing beta-propeller protein-associated neurodegeneration.
000495 (2014)	Julia Ziegan [Allemagne] ; Matthias Wittstock ; Ana Westenberger ; Valerija Dobri I ; Alexander Wolters ; Reiner Benecke ; Christine Klein ; Christoph Kamm	Novel GNAL mutations in two German patients with sporadic dystonia.
000557 (2014)	S. Tunc ; P. Capetian ; Alexander Münchau	Hope for Huntington's disease? A novel approach for disease modification.
000579 (2014)	Bettina Balint [Allemagne] ; Kailash P. Bhatia	Friend or foe? IgLON5 antibodies in a novel tauopathy with prominent sleep movement disorder, ataxia, and chorea.
000627 (2014)	Fu-Bo Cheng [République populaire de Chine] ; Jia-Chun Feng ; Ling-Yan Ma ; Jing Miao ; Thomas Ott ; Xin-Hua Wan ; Kathrin Grundmann	Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia.
000657 (2014)	E. Mulroy [Irlande (pays)] ; A. Mccarthy [Irlande (pays)] ; D. Costello [Irlande (pays)] ; Oa Ross [États-Unis] ; T. Lynch [Irlande (pays)]	Asymmetrical leg atrophy in Dopa Responsive Dystonia due to a novel GTP cyclohydrolase mutation
000684 (2014)	Eiichi Araki [Japon] ; Yoshio Tsuboi ; Justus Daechsel ; Austen Milnerwood ; Carles Vilarino-Guell ; Naoki Fujii ; Takayasu Mishima ; Takayuki Oka ; Hideo Hara ; Jiro Fukae ; Matthew J. Farrer	A novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy.
000794 (2013)	Darius Ebrahimi-Fakhari [Allemagne] ; Lara Wahlster	Restoring impaired protein metabolism in Parkinson's disease--TFEB-mediated autophagy as a novel therapeutic target.

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