Spontané < Sporadique < Sport

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List of bibliographic references indexed by Sporadique

Number of relevant bibliographic references: 46.
[0-20] [0 - 20][0 - 46][20-40]

Ident.	Authors (with country if any)	Title
001053 (2012)	Kurt A. Jellinger [Autriche]	Neuropathology of Sporadic Parkinson's Disease: Evaluation and Changes of Concepts
001057 (2012)	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
001073 (2012)	Kelly Del Tredici [Allemagne] ; Heiko Braak [Allemagne]	Lewy Pathology and Neurodegeneration in Premotor Parkinson's Disease
001184 (2012)	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
001213 (2012)	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
001949 (2010)	Ted M. Dawson [États-Unis] ; Valina L. Dawson [États-Unis]	The role of parkin in familial and sporadic Parkinson's disease
001995 (2010)	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
002281 (2009)	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
002296 (2009)	Susanne A. Schneider [Royaume-Uni] ; Coro Paisan-Ruiz [Royaume-Uni] ; Ines Garcia-Gorostiaga [Royaume-Uni, Espagne] ; Niall P. Quinn [Royaume-Uni] ; Yvonne G. Weber ; Holger Lerche [Allemagne] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]	GLUT1 gene mutations cause sporadic paroxysmal exercise‐induced dyskinesias
002351 (2009)	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?
002379 (2009)	Helen Ling [Thaïlande] ; Kanjana Unnwongse [Thaïlande] ; Roongroj Bhidayasiri [Thaïlande]	Complex movement disorders in a sporadic Boucher‐Neuhäuser Syndrome: Phenotypic manifestations beyond the triad
002576 (2008)	Christopher H. Hawkes [Royaume-Uni]	The prodromal phase of sporadic Parkinson's disease: Does it exist and if so how long is it?
002602 (2008)	Giacomina Rossi [Italie] ; Cecilia Marelli [Italie] ; Laura Farina [Italie] ; Matilde Laurà [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
002791 (2008)	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
002952 (2008)	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
002E16 (2007)	Joaquim J. Ferreira [Portugal, Pays-Bas] ; Leonor Correia Guedes [Portugal] ; Mário 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
002E22 (2007)	Michael Abele [Allemagne] ; Thomas Klockgether [Allemagne]	Health‐related quality of life in sporadic adult‐onset ataxia
003156 (2006)	Juan J. Zarranz [Espagne] ; Juan C. G Mez-Esteban [Espagne] ; Bego A Atarés [Espagne] ; Elena Lezcano [Espagne] ; Maribel Forcadas [Espagne]	Tau‐predominant–associated pathology in a sporadic late‐onset Hallervorden–Spatz syndrome
003181 (2006)	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
003183 (2006)	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
003224 (2006)	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

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