Biologie moléculaire And NotPatrizla Tarugi

List of bibliographic references

Number of relevant bibliographic references: 13.

Ident.	Authors (with country if any)	Title
002404	Thomas Gasser [Allemagne] ; Susan Bressman [États-Unis] ; Alexandra Dürr [France] ; Joseph Higgins [États-Unis] ; Thomas Klockgether [Allemagne] ; Richard H. Myers [États-Unis]	Molecular diagnosis of inherited movement disorders. Movement disorders Society Task Force on Molecular Diagnosis
002447	HYUN SOOK KIM [Corée du Sud] ; MYUNG SIK LEE [Corée du Sud]	Frequencies of single nucleotide polymorphism in alcohol dehydrogenase7 gene in patients with multiple system atrophy and controls
002491	Ruth H. Walker [États-Unis] ; P. Shashidharan [États-Unis]	Developments in the molecular biology of DYT1 dystonia
002745	Pau Pastor [Espagne] ; Mario Ezquerra [Espagne] ; Eduardo Tolosa [Espagne] ; Esteban Munoz [Espagne] ; Maria José Marti [Espagne] ; Francesc Valldeoriola [Espagne] ; José Luis Molinuevo [Espagne] ; Matilde Calopa [Espagne] ; Rafael Oliva [Espagne]	Further extension of the H1 haplotype associated with progressive supranuclear palsy
002957	Massimo Pandolfo [Canada]	Molecular basis of friedreich ataxia
002B01	T. Klockgether [Allemagne] ; U. Wüllner [Allemagne] ; A. Spauschus [Royaume-Uni] ; B. Evert [Allemagne]	The molecular biology of the autosomal-dominant cerebellar ataxias
002B02	Alain Destée [France] ; Isabelle Delalande [France] ; Isabelle Vuillaume [France] ; Susanna Schraen-Maschke [France] ; Luc Defebvre [France] ; Bernard Sablonniere [France]	The first identified French family with dentatorubral-pallidoluysian atrophy
002B09	Christoph Kamm [Allemagne] ; Markus Naumann [Allemagne] ; Joerg Mueller [Autriche] ; Norbert Mai [Allemagne] ; Leonhard Riedel [Allemagne] ; Joerg Wissel [Autriche] ; Thomas Gasser [Allemagne]	The DYT1 GAG deletion is infrequent in sporadic and familial writer's cramp
002C36	Sergei N. Illarioshkin [Russie] ; Irina A. Ivanova-Smolenskaya [Russie] ; Rahmatullo A. Rahmonov [Russie] ; Elena D. Markova [Russie] ; Giovanni Stevanin [France] ; Alexis Brice [France]	Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan
002C70	Silvia Buervenich [Suède] ; Olof Sydow [Suède] ; Andrea Carmine [Suède] ; ZHIPING ZHANG [Suède] ; Maria Anvret [Suède] ; Lars Olson [Suède]	Alcohol dehydrogenase alleles in Parkinson's disease
002C85	M. Neystat [États-Unis] ; T. Lynch [États-Unis] ; S. Przedborski [États-Unis] ; N. Kholodilov [États-Unis] ; M. Rzhetskaya [États-Unis] ; R. E. Burke [États-Unis]	α-Synuclein expression in substantia nigra and cortex in Parkinson's disease
002E29	L. Sudarsky [États-Unis] ; G. M. Plotkin [États-Unis] ; E. L. Logigian [États-Unis] ; D. R. Johns [États-Unis]	Dystonia as a presenting feature of the 3243 mitochondrial DNA mutation
003001	E. Silber [Afrique du Sud] ; J. Kromberg [Afrique du Sud] ; J. A. Temlett [Afrique du Sud] ; A. Krause [Afrique du Sud] ; D. Saffer [Afrique du Sud]	Huntington's disease confirmed by genetic testing in five African families

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