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List of bibliographic references indexed by novo

Number of relevant bibliographic references: 32.
[0-20] [0 - 20][0 - 32][20-31][20-40]

Ident.	Authors (with country if any)	Title
000145 (2015)	Roberto Erro [Italie] ; Marina Picillo ; Marianna Amboni ; Marcello Moccia ; Carmine Vitale ; Katia Longo ; Maria Teresa Pellecchia ; Gabriella Santangelo ; Pablo Martinez-Martin ; K Ray Chaudhuri ; Paolo Barone	Nonmotor predictors for levodopa requirement in de novo patients with Parkinson's disease.
000277 (2015)	Zhong-Bin Zhang [République populaire de Chine] ; Mao-Qiang Tian [République populaire de Chine] ; Kai Gao [République populaire de Chine] ; Yu-Wu Jiang [République populaire de Chine] ; Ye Wu [République populaire de Chine]	De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay.
000284 (2015)	Tanya Simuni [États-Unis] ; Chelsea Caspell-Garcia [États-Unis] ; Christopher Coffey [États-Unis] ; Lama M. Chahine [États-Unis] ; Shirley Lasch [États-Unis] ; Wolfgang H. Oertel [Allemagne] ; Geert Mayer ; Birgit Högl [Autriche] ; Ron Postuma [Canada] ; Aleksandar Videnovic [États-Unis] ; Amy Willis Amara [États-Unis] ; Ken Marek [États-Unis]	Correlates of excessive daytime sleepiness in de novo Parkinson's disease: A case control study.
000352 (2015)	Raphael Carapito [France] ; Nicodème Paul ; Meiggie Untrau ; Marion Le Gentil ; Louise Ott ; Ghada Alsaleh ; Pierre Jochem ; Mirjana Radosavljevic ; Cédric Le Caignec ; Albert David ; Philippe Damier ; Bertrand Isidor ; Seiamak Bahram	A de novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystonia.
000609 (2014)	Valerija Dobri I [Allemagne] ; Nikola Kresojevi ; Ana Westenberger ; Marina Svetel ; Aleksandra Tomi ; Vesna Rali ; Igor Petrovi ; Milica Je Menica Luki ; Katja Lohmann ; Ivana Novakovi ; Christine Klein ; Vladimir S. Kosti	De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient.
000632 (2014)	Françoise J. Siepel [Norvège] ; Kolbj Rn S. Br Nnick ; Jan Booij ; Bernard M. Ravina ; Alexander V. Lebedev ; Joana B. Pereira ; Renate Grüner ; Dag Aarsland	Cognitive executive impairment and dopaminergic deficits in de novo Parkinson's disease.
000A37 (2013)	Eugenia Storti ; Francesca Cortese ; Roberto Di Fabio ; Chiara Fiorillo ; Alberto Pierallini ; Alessandra Tessa ; Annamaria Valleriani ; Francesco Pierelli ; Filippo M. Santorelli ; Carlo Casali	De novo FTL mutation: a clinical, neuroimaging, and molecular study.
000A38 (2013)	Athanasia Alexoudi [Allemagne] ; Susanne A. Schneider	De Novo mutations in the β-tubulin gene TUBB4: from DYT4 to leukoencephalopathy with hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC syndrome).
000B34 (2013)	Judith Van Gaalen [Pays-Bas] ; Sascha Vermeer ; Marjon Van Veluw ; Bart P C. Van De Warrenburg ; Dennis Dooijes	A de novo SCA14 mutation in an isolated case of late-onset cerebellar ataxia.
000D11 (2012)	Michele Poletti ; Daniela Frosini ; Roberto Ceravolo ; Ubaldo Bonuccelli	Mild cognitive impairment in De Novo Parkinson's disease according to movement disorder guidelines.
000D40 (2012)	Michele Poletti ; Daniela Frosini ; Claudio Lucetti ; Paolo Del Dotto ; Roberto Ceravolo ; Ubaldo Bonuccelli	Iowa Gambling Task in de novo Parkinson's disease: a comparison between good and poor performers.
001A17 (2010)	Patricia De Carvalho Aguiar [Brésil] ; Tania Fuchs [États-Unis] ; Vanderci Borges [Brésil] ; Kay-Marie Lamar [États-Unis] ; Sonia Maria Azevedo Silva [Brésil] ; Henrique Ballalai Ferraz [Brésil] ; Laurie Ozelius [États-Unis]	Screening of Brazilian families with primary dystonia reveals a novel THAP1 mutation and a de novo TOR1A GAG deletion
001C43 (2010)	Paola S. Denora [France, Italie] ; Knut Brockmann [Allemagne] ; Marianna Ciccolella [Italie] ; Jeremy Truchetto [France] ; Giovanni Stevanin [France, Italie] ; Filippo M. Santorelli [Italie]	Identification of a de novo mutation in SPG11
001D65 (2010)	Michele Poletti [Italie] ; Daniela Frosini [Italie] ; Claudio Lucetti [Italie] ; Paolo Del Dotto [Italie] ; Roberto Ceravolo [Italie] ; Ubaldo Bonuccelli [Italie]	Decision making in de novo Parkinson's disease
001D81 (2010)	Flavio Nobili [Italie] ; Claudio Campus [Italie] ; Dario Arnaldi [Italie] ; Fabrizio De Carli [Italie] ; Gaia Cabassi [Italie] ; Andrea Brugnolo [Italie] ; Barbara Dessi [Italie] ; Silvia Morbelli [Italie] ; Gianmario Sambuceti [Italie] ; Giovanni Abbruzzese [Italie] ; Guido Rodriguez [Italie]	Cognitive‐nigrostriatal relationships in de novo, drug‐naïve Parkinson's disease patients: A [I‐123]FP‐CIT SPECT study
001E30 (2010)	Janey Prodoehl [États-Unis] ; Mathew Spraker [États-Unis] ; Daniel Corcos [États-Unis] ; Cynthia Comella [États-Unis] ; David Vaillancourt [États-Unis]	Blood oxygenation level–dependent activation in basal ganglia nuclei relates to specific symptoms in de novo Parkinson's disease
002804 (2008)	Hoon-Chul Kang [Corée du Sud] ; Su Jeong You [Corée du Sud] ; Myung Jae Chey [Corée du Sud] ; Jong Sam Baik [Corée du Sud] ; Jong-Won Kim [Corée du Sud] ; Chang-Seok Ki [Corée du Sud]	Identification of a de novo Lys304Gln mutation in the glycine receptor α‐1 subunit gene in a Korean infant with hyperekplexia
002D11 (2007)	Vanderci Borges [Brésil] ; Patricia De Carvalho Aguiar [Brésil] ; Henrique Ballalai Ferraz [Brésil] ; Laurie J. Ozelius [États-Unis]	Novel and de novo mutations of the SGCE gene in Brazilian patients with myoclonus‐dystonia
003691 (2005)	Katherine Grosset [Royaume-Uni] ; Donald Grosset [Royaume-Uni] ; Andrew Lees (neurologue) [Royaume-Uni]	Trial of subtherapeutic pergolide in de novo Parkinson's disease
003995 (2005)	Stephane Thobois [Royaume-Uni, France] ; Stephen Tisch [Royaume-Uni] ; Jing Xie-Brustolin [France] ; Patrick Mertens [France] ; Marwan I. Hariz [Royaume-Uni] ; Isabelle Benatru [France] ; Emmanuel Broussolle [France] ; Patricia Limousin-Dowsey [Royaume-Uni]	Can chronic subthalamic nucleus stimulation induce de novo tremor in Parkinson's disease?
003D00 (2004)	Stuart J. Fellows ; Johannes Noth	Grip force abnormalities in de novo Parkinson's disease

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