Membrane Potentials < Membrane Proteins < Membrane Transport Proteins

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List of bibliographic references

Number of relevant bibliographic references: 25.
[0-20] [0 - 20][0 - 25][20-24][20-40]

Ident.	Authors (with country if any)	Title
000585 (2001)	A. Danek [Allemagne] ; F. Tison ; J. Rubio ; M. Oechsner ; W. Kalckreuth ; A P Monaco	The chorea of McLeod syndrome.
000D66 (2004)	Dorothy D. Whelchel [États-Unis] ; Tonia M. Brehmer ; Paula M. Brooks ; Neely Darragh ; Julie A. Coffield	Molecular targets of botulinum toxin at the mammalian neuromuscular junction.
000D68 (2004)	Ester Fernández-Salas [États-Unis] ; Helen Ho ; Patton Garay ; Lance E. Steward ; K Roger Aoki	Is the light chain subcellular localization an important factor in botulinum toxin duration of action?
000D70 (2004)	John A. Chaddock [Royaume-Uni] ; John R. Purkiss ; Frances C G. Alexander ; Sarah Doward ; Sarah J. Fooks ; Lorna M. Friis ; Yper H J. Hall ; Elizabeth R. Kirby ; Nicola Leeds ; Hilary J. Moulsdale ; Anthony Dickenson ; G Mark Green ; Wahida Rahman ; Rie Suzuki ; Michael J. Duggan ; Conrad P. Quinn ; Clifford C. Shone ; Keith A. Foster	Retargeted clostridial endopeptidases: inhibition of nociceptive neurotransmitter release in vitro, and antinociceptive activity in in vivo models of pain.
001224 (2005)	C Warren Olanow [États-Unis] ; Joseph Jankovic [États-Unis]	Neuroprotective therapy in Parkinson's disease and motor complications: a search for a pathogenesis-targeted, disease-modifying strategy.
001396 (2006)	Alberto L. Rosa [Argentine] ; Irma Molina ; Valeria Kowaljow ; Cecilia B. Conde	Brisk deep-tendon reflexes as a distinctive phenotype in an Argentinean spinocerebellar ataxia type 2 pedigree.
001530 (2006)	Renato P. Munhoz [Brésil] ; Toshitaka Kawarai ; Helio A. Teive ; Salmo Raskin ; Christine Sato ; Yan Liang ; Peter H. St George-Hyslop ; Ekaterina Rogaeva	Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus).
001750 (2006)	Satoshi Kaneko [Japon] ; Toshitaka Kawarai ; Edwin Yip ; Shabnam Salehi-Rad ; Christine Sato ; Antonio Orlacchio ; Giorgio Bernardi ; Yan Liang ; Hiroshi Hasegawa ; Ekaterina Rogaeva ; Peter St George-Hyslop	Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia.
001770 (2006)	Toshiaki Takahashi [Japon] ; Masashi Aoki ; Takashi Imai ; Masaru Yoshioka ; Hidehiko Konno ; Shuichi Higano ; Yoshiaki Onodera ; Hiroshi Saito ; Itaru Kimura ; Yasuto Itoyama	A case of dysferlinopathy presenting choreic movements.
001E02 (2007)	Soraya Bardien [Afrique du Sud] ; Fatima Abrahams ; Himla Soodyall ; Lize Van Der Merwe ; Jacquie Greenberg ; Tinus Brink ; Jonathan Carr	A South African mixed ancestry family with Huntington disease-like 2: clinical and genetic features.
001E07 (2007)	Giovanni Fabbrini [Italie] ; Massimo Pasquini ; Cinzia Aurilia ; Isabella Berardelli ; Guido Breedveld ; Ben A. Oostra ; Vincenzo Bonifati ; Alfredo Berardelli	A large Italian family with Gilles de la Tourette syndrome: clinical study and analysis of the SLITRK1 gene.
002021 (2008)	Edward J. Wild [Royaume-Uni] ; Ese E. Mudanohwo ; Mary G. Sweeney ; Susanne A. Schneider ; Jon Beck ; Kailash P. Bhatia ; Martin N. Rossor ; Mary B. Davis ; Sarah J. Tabrizi	Huntington's disease phenocopies are clinically and genetically heterogeneous.
002090 (2008)	Bart P C. Van De Warrenburg [Royaume-Uni] ; Andrew J. Church ; Davide Martino ; Paul M. Candler ; Kailash P. Bhatia ; Gavin Giovannoni ; Niall P. Quinn	Antineuronal antibodies in Parkinson's disease.
002352 (2008)	Guilherme G Riccioppo Rodrigues ; Ruth H. Walker ; Alexis Brice ; Cécile Cazeneuve ; Odile Russaouen ; Helio A G. Teive ; Renato Puppi Munhoz ; Nilson Becker ; Salmo Raskin ; Lineu Cesar Werneck ; Wilson Marques Junior ; Vitor Tumas	Huntington's disease-like 2 in Brazil--report of 4 patients.
002887 (2009)	Dietrich Haubenberger [Autriche] ; Christoph Hotzy [Autriche] ; Walter Pirker [Autriche] ; Regina Katzenschlager [Autriche] ; Thomas Brücke [Autriche] ; Fritz Zimprich [Autriche] ; Eduard Auff [Autriche] ; Alexander Zimprich [Autriche]	Role of LINGO1 polymorphisms in Parkinson’s disease
002B19 (2010)	Sandra Thier [Allemagne] ; Delia Lorenz ; Michael Nothnagel ; Giovanni Stevanin ; Alexandra Dürr ; Almut Nebel ; Stefan Schreiber ; Gregor Kuhlenb Umer ; Günther Deuschl ; Stephan Klebe	LINGO1 polymorphisms are associated with essential tremor in Europeans.
003156 (2011)	Oswaldo Lorenzo-Betancor [Espagne] ; Lluís Samaranch ; Elena García-Martín ; Sebastián Cervantes ; José A G. Agúndez ; Félix J. Jiménez-Jiménez ; Hortensia Alonso-Navarro ; Antonio Luengo ; Francisco Coria ; Elena Lorenzo ; Jaione Irigoyen ; Pau Pastor	LINGO1 gene analysis in Parkinson's disease phenotypes.
003301 (2011)	Benjamin Dehay	α-synuclein, a prion-like protein.
003909 (2012)	Anne Weissbach [Allemagne] ; Katharina Siegesmund ; Norbert Brüggemann ; Alexander Schmidt ; Meike Kasten ; Irene Pichler ; Hiltrud Muhle ; Ebba Lohmann ; Thora Lohnau ; Eberhard Schwinger ; Johann Hagenah ; Ulrich Stephani ; Peter P. Pramstaller ; Christine Klein ; Katja Lohmann	Exome sequencing in a family with restless legs syndrome.
003A52 (2013)	Yi-Chun Chen [Taïwan] ; Yun-Shien Lee ; Chen-Chang Shih ; Tony Wu ; Chiung-Mei Chen	Mutations of proline-rich transmembrane protein-2 and paroxysmal kinesigenic dyskinesia in Taiwan.
003A76 (2013)	Chang-He Shi ; Shi-Lei Sun ; Jun-Ling Wang ; Ai-Qin Liu ; Wang Miao ; Chandra Avinash ; Xiao Mao ; Bei-Sha Tang ; Yu-Ming Xu	PRRT2 gene mutations in familial and sporadic paroxysmal kinesigenic dyskinesia cases.

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