Sporadique And NotDaniel G. Healy

List of bibliographic references

Number of relevant bibliographic references: 45.

Ident.	Authors (with country if any)	Title
000126	Kurt A. Jellinger [Autriche]	Neuropathology of Sporadic Parkinson's Disease: Evaluation and Changes of Concepts
000130	Brent L. Fogel [États-Unis] ; JI YONG LEE [États-Unis] ; Jessica Lane [États-Unis] ; Amanda Wahnich [États-Unis] ; Sandy Chan [États-Unis] ; Alden Huang [États-Unis] ; Greg E. Osborn [États-Unis] ; Eric Klein [États-Unis] ; Catherine Mamah [États-Unis] ; Susan Perlman [États-Unis] ; Daniel H. Geschwind [États-Unis] ; Giovanni Coppola [États-Unis]	Mutations in Rare Ataxia Genes Are Uncommon Causes of Sporadic Cerebellar Ataxia
000146	Kelly Del Tredici [Allemagne] ; Heiko Braak [Allemagne]	Lewy Pathology and Neurodegeneration in Premotor Parkinson's Disease
000257	Brent L. Fogel [États-Unis] ; Mochtar Pribadi [États-Unis] ; Sarah Pi [États-Unis] ; Susan L. Perlman [États-Unis] ; Daniel H. Geschwind [États-Unis] ; Giovanni Coppola [États-Unis]	C9ORF72 Expansion Is Not a Significant Cause of Sporadic Spinocerebellar Ataxia
000286	Elena V. Semenova [Russie] ; Maria I. Shadrina [Russie] ; Pyotr A. Slominsky [Russie] ; Irina A. Ivanova-Smolenskaya [Russie] ; Gulbakhar Bagyeva [Russie] ; Sergei N. Illarioshkin [Russie] ; Svetlana A. Limborska [Russie]	Analysis of PARK2 Gene Exon Rearrangements in Russian Patients with Sporadic Parkinson's Disease
000784	Ted M. Dawson [États-Unis] ; Valina L. Dawson [États-Unis]	The Role of Parkin in Familial and Sporadic Parkinson's Disease
000826	Alessandro Brussino [Italie] ; Claudio Graziano [Italie] ; Dario Giobbe [Italie] ; Marina Ferrone [Italie] ; Elisa Dragone [Italie] ; Carlo Arduino [Italie] ; Raffaele Lodi [Italie] ; Caterina Tonon [Italie] ; Anna Gabellini [Italie] ; Rita Rinaldi [Italie] ; Sara Miccoli [Italie] ; Enrico Grosso [Italie] ; Maria Cristina Bellati [Italie] ; Laura Orsi [Italie] ; Nicola Migone [Italie] ; Alfredo Brusco [Italie]	Spinocerebellar Ataxia Type 12 Identified in Two Italian Families May Mimic Sporadic Ataxia
000E57	Greg T. Sutherland [Australie] ; Gerhard A. Siebert [Australie] ; Jeremy R. B. Newman [Australie] ; Peter A. Silburn [Australie] ; Richard S. Boyle [Australie] ; John D. O'Sullivan [Australie] ; George D. Mellick [Australie]	Haplotype Analysis of the PARK 11 Gene, GIGYF2, in Sporadic Parkinson's Disease
000E69	Susanne A. Schneider [Royaume-Uni] ; Coro Paisan-Ruiz [Royaume-Uni] ; Ines Garcia-Gorostiaga [Royaume-Uni, Espagne] ; Niall P. Quinn [Royaume-Uni] ; Yvonne G. Weber [Allemagne] ; Holger Lerche [Allemagne] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]	GLUT1 Gene Mutations Cause Sporadic Paroxysmal Exercise-Induced Dyskinesias
000F11	Greg T. Sutherland [Australie] ; Glenda M. Halliday [Australie] ; Peter A. Silburn [Australie] ; Frank L. Mastaglia [Australie] ; Dominic B. Rowe [Australie] ; Richard S. Boyle [Australie] ; John D. O'Sullivan [Australie] ; Tina Ly [Australie] ; Steve D. Wilton [Australie] ; George D. Mellick [Australie]	Do Polymorphisms in the Familial Parkinsonism Genes Contribute to Risk for Sporadic Parkinson's Disease?
000F33	Helen Ling [Thaïlande] ; Kanjana Unnwongse [Thaïlande] ; Roongroj Bhidayasiri [Thaïlande]	Complex Movement Disorders in a Sporadic Boucher-Neuhäuser Syndrome: Phenotypic Manifestations Beyond the Triad
001051	Christopher H. Hawkes [Royaume-Uni]	The Prodromal Phase of Sporadic Parkinson's Disease : Does It Exist and If So How Long Is It?
001061	Giacomina Rossi [Italie] ; Cecilia Marelli [Italie] ; Laura Farina [Italie] ; Matilde Laura [Italie] ; Anna Maria Basile [Italie] ; Claudia Ciano [Italie] ; Fabrizio Tagliavini [Italie] ; Davide Pareyson [Italie]	The G389R Mutation in the MAPT Gene Presenting as Sporadic Corticobasal Syndrome
001214	Vania Gelmetti [Italie] ; Alessandro Ferraris [Italie] ; Livia Brusa [Italie] ; Francesca Romano [Italie] ; Federica Lombardi [Italie] ; Chiara Barzaghi [Italie] ; Paolo Stanzione [Italie] ; Barbara Garavaglia [Italie] ; Bruno Dallapiccola [Italie] ; Enza Maria Valente [Italie]	Late Onset Sporadic Parkinson's Disease Caused by PINK1 Mutations : Clinical and Functional Study
001332	Marios Hadjivassiliou [Royaume-Uni] ; Sabrina Boscolo [Italie] ; Enrico Tongiorgi [Italie] ; Richard A. Grünewald [Royaume-Uni] ; Basil Sharrack [Royaume-Uni] ; David S. Sanders [Royaume-Uni] ; Nicola Woodroofe [Royaume-Uni] ; G. Aelwyn B. Davies-Jones [Royaume-Uni]	Cerebellar Ataxia as a Possible Organ-Specific Autoimmune Disease
001649	Joaquim J. Ferreira [Portugal] ; Leonor Correia Guedes [Portugal] ; Mario Miguel Rosa [Portugal] ; Miguel Coelho [Portugal] ; Marina Van Doeselaar [Pays-Bas] ; Dorothea Schweiger [Pays-Bas] ; Alessio Di Fonzo [Pays-Bas] ; Ben A. Oostra [Pays-Bas] ; Cristina Sampaio [Portugal] ; Vincenzo Bonifati [Pays-Bas]	High prevalence of LRRK2 mutations in familial and sporadic parkinson's disease in portugal
001653	Michael Abele [Allemagne] ; Thomas Klockgether [Allemagne]	Health-related quality of life in sporadic adult-onset ataxia
001874	Juan J. Zarranz [Espagne] ; Juan C. Gomez-Esteban [Espagne] ; Begona Atares [Espagne] ; Elena Lezcano [Espagne] ; Maribel Forcadas [Espagne]	Tau-predominant-associated pathology in a sporadic late-onset Hallervorden-Spatz syndrome
001895	Heiko Braak [Allemagne] ; Jürgen R. Bohl [Allemagne] ; Christian M. Müller [Allemagne] ; Udo Rüb [Allemagne] ; Rob A. I. De Vos [Pays-Bas] ; Kelly Del Tredici [Allemagne]	Stanley fahn lecture 2005 : The staging procedure for the inclusion body pathology associated with sporadic Parkinson's disease reconsidered
001897	Daan J. Kamphuis [Pays-Bas] ; Hans Koelman [Pays-Bas] ; Andrew Lees (neurologue) [Royaume-Uni] ; Marina A. J. Tijssen [Pays-Bas]	Sporadic rapid-onset dystonia-parkinsonism presenting as Parkinson's disease
001927	Alberto J. Espay [Canada, États-Unis] ; Catherine Bergeron [Canada] ; Robert Chen [Canada] ; Anthony E. Lang [Canada]	Rapidly progressive sporadic dentatorubral pallidoluysian atrophy with intracytoplasmic inclusions and no CAG repeat expansion
001983	Eng-King Tan [Singapour] ; Kenneth Yew [Singapour] ; Eva Chua [Singapour] ; K. Puvan [Singapour] ; HUI SHEN [Singapour] ; Esther Lee [Singapour] ; Kim-Yoong Puong [Singapour] ; YI ZHAO [Singapour] ; Ratnagopal Pavanni [Singapour] ; Meng-Cheong Wong [Singapour] ; Dominic Jamora [Singapour] ; Deidre De Silva [Singapour] ; Kyaw-Thu Moe [Singapour] ; Fung-Peng Woon [Singapour] ; YIH YUEN [Singapour] ; Louis Tan [Singapour]	PINK1 mutations in sporadic early-onset parkinson's disease
001999	Alfonso Fasano [Italie] ; Nardo Nardocci [Italie] ; Antonio Emanuele Elia [Italie] ; Giovanna Zorzi [Italie] ; Anna Rita Bentivoglio [Italie] ; Alberto Albanese [Italie]	Non-DYT1 early-onset primary torsion dystonia : Comparison with DYT1 phenotype and review of the literature
001A13	Peter Bauer [Allemagne] ; Friedmar R. Kreuz [Allemagne] ; Katrin Bürk [Allemagne] ; Carsten Saft [Allemagne] ; Jürgen Andrich [Allemagne] ; Hubert Heilemann [Allemagne] ; Olaf Riess [Allemagne] ; Ludger Schöls [Allemagne]	Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause
001A21	Stephan Klebe [Allemagne] ; Günther Deuschl [Allemagne] ; Henning Stolze [Allemagne]	Methylphenidate fails to improve gait and muscle tone in patients with sporadic and hereditary spastic paraplegia
001A34	Omit Chiba-Falek [États-Unis] ; Grisel J. Lopez [États-Unis] ; Robert L. Nussbaum [États-Unis]	Levels of alpha-synuclein mRNA in sporadic parkinson disease patients
001A35	Andrea Carmine Belin [Suède] ; Marie Westerlund [Suède] ; Olof Sydow [Suède] ; Karin Lundströmer [Suède] ; Anna Hakansson [Suède] ; Hans Nissbrandt [Suède] ; Lars Olson [Suède] ; Dagmar Gaiter [Suède]	Leucine-rich repeat kinase 2 (LRRK2) mutations in a Swedish parkinson cohort and a healthy nonagenarian
001A39	Hon-Chung Fung [États-Unis, Royaume-Uni, Taïwan] ; Chiung-Mei Chen [Taïwan] ; John Hardy [États-Unis, Royaume-Uni] ; Dena Hernandez [États-Unis] ; Andrew Singleton [États-Unis] ; Yih-Ru Wu [Taïwan]	Lack of G2019S LRRK2 mutation in a cohort of taiwanese with sporadic parkinson's disease
001A63	Hideaki Kobayashi [Japon] ; Hiroshi Ujike [Japon] ; Junko Hasegawa [Japon] ; Mitsutoshi Yamamoto [Japon] ; Akihiro Kanzaki [Japon] ; Ichiro Sora [Japon]	Identification of a risk haplotype of the α-synuclein gene in japanese with sporadic Parkinson's disease
001A89	Sofya N. Pchelina [Russie] ; Andrei F. Yakimovskii [Russie] ; Olga N. Ivanova [Russie] ; Anton K. Emelianov [Russie] ; Andrei H. Zakharchuk [Russie] ; Alexander L. Schwarzman [Russie]	G2019S LRRK2 mutation in familial and sporadic Parkinson's disease in Russia
001D09	Angela Deutschl Nder [Allemagne] ; Friedrich Asmus [Allemagne] ; Thomas Gasser [Allemagne] ; Ulrich Steude [Allemagne] ; Kai Bötzel [Allemagne]	Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation
001E44	Jeong-Hyun Kim [Corée du Sud] ; Yoon-Hee Cho [Corée du Sud] ; Jeong-Kook Kim [Corée du Sud] ; Yong-Gou Park [Corée du Sud] ; JIN WOO CHANG [Corée du Sud]	Frequent sequence variation at the ETM2 locus and its association with sporadic essential tremor in Korea
001F17	Masataka Nishimura [Japon] ; Sadako Kuno [Japon] ; Ryuji Kaji [Japon] ; Hideshi Kawakami [Japon]	Brain-derived neurotrophic factor gene polymorphisms in Japanese patients with sporadic Alzheimer's disease, Parkinson's disease, and multiple system atrophy
001F38	Eng-King Tan [Singapour] ; Van R. Chandran [Singapour] ; Stephanie Fook-Chong [Singapour] ; HUI SHEN [Singapour] ; F. Kenneth Yew [Singapour] ; Mei-Lin Teoh [Singapour] ; YI ZHAO [Singapour]	Alpha-synuclein mRNA expression in sporadic Parkinson's disease
001F39	Kevin J. Klos [États-Unis] ; Keith A. Josephs [États-Unis] ; Joseph E. Parisi [États-Unis] ; Dennis W. Dickson [États-Unis]	Alpha-synuclein immunohistochemistry in two cases of co-occurring idiopathic Parkinson's disease and motor neuron disease
001F95	Renato P. Munhoz [Canada] ; Catherine Bergeron [Canada] ; Anthony E. Lang [Canada]	Sporadic case of dentatorubral pallidoluysian atrophy with no CAG repeat expansion and no intranuclear inclusions
002047	Din-E. Shan [Taïwan] ; Ren-Shyan Liu [Taïwan] ; Chen-Ming Sun [Taïwan] ; Shwn-Jen Lee [Taïwan] ; Kwong-Kum Liao [Taïwan] ; Bing-Wen Soong [Taïwan]	Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: Clinical implications
002428	Masataka Nishimura [Japon] ; Sadako Kuno [Japon] ; Ikuko Mizuta [Japon] ; Mitsuhiro Ohta [Japon] ; Hirofumi Maruyama [Japon] ; Ryuji Kaji [Japon] ; Hideshi Kawakami [Japon]	Influence of monocyte chemoattractant protein 1 gene polymorphism on age at onset of sporadic Parkinson's disease
002580	Peter Brown [Royaume-Uni]	The startle syndrome
002651	Gurutz Linazasoro [Espagne] ; Begona Indakoetxea [Espagne] ; Javier Ruiz [Espagne] ; Nadege Van Blercom [Espagne] ; Asier Lasa [Espagne]	Possible sporadic rapid-onset dystonia-parkinsonism
002652	Pauline L. Lee [États-Unis] ; Terri Gelbart [États-Unis] ; Carol West [États-Unis] ; Carol Halloran [États-Unis] ; Jack C. Sipe [États-Unis] ; Ernest Beutler [États-Unis]	Polymorphisms in iron-responsive binding protein 2 and lack of association with sporadic Parkinson's disease
002750	Giovanna Zorzi [Italie] ; Barbara Garavaglia [Italie] ; Federica Invernizzi [Italie] ; Floriano Girotti [Italie] ; Paola Soliveri [Italie] ; Massimo Zeviani [Italie] ; Lucia Angelini [Italie] ; Nardo Nardocci [Italie]	Frequency of DYT1 mutation in early-onset primary dystonia in Italian patients
002B35	K. F. Bhattacharya [Royaume-Uni] ; I. Giannakikou [Royaume-Uni] ; N. Munroe [Royaume-Uni] ; K. Ray Chaudhuri [Royaume-Uni]	Primary anticholinergic-responsive pisa syndrome
002B67	J. N. Caviness [États-Unis] ; B. E. Smith [États-Unis] ; J. C. Stevens [États-Unis] ; C. H. Adler [États-Unis] ; R. J. Caselli [États-Unis] ; C. A. Reiners [États-Unis] ; J. G. Hentz [États-Unis] ; M. D. Muenter [États-Unis]	Motor unit changes in sporadic idiopathic Parkinson's disease
003012	S.-L. Ho [Hong Kong] ; M. H. W. Kung [Hong Kong]	G209A mutation in the α-synuclein gene is rare and not associated with sporadic Parkinson's disease

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	Movement Disorders (revue)
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Movement Disorders (revue)

Sporadique And NotDaniel G. Healy

List of bibliographic references