Chorea (etiology) < Chorea (genetics) < Chorea (history)

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List of bibliographic references indexed by Chorea (genetics)

Number of relevant bibliographic references: 55.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000006 (2015)	Mark Hallett [États-Unis] ; Jose Obeso	Where does chorea come from? cortical excitability findings challenge classic pathophysiological concepts.
000485 (2014)	Roberto Erro [Royaume-Uni] ; Una-Marie Sheerin ; Kailash P. Bhatia	Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.
000866 (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.
000963 (2013)	Laura Dosa ; Alessandro Malandrini ; Ilaria Di Donato ; Uros Hladnik ; Ilaria Meloni ; Francesca Mari ; Antonio Federico	Huntington's disease gene expansion associates with early onset nonprogressive chorea.
000A80 (2013)	Virginie Lambrecq ; Florence Riant ; Elisabeth Tournier-Lasserve ; Véronique Michel ; Pierre Burbaud	Caffeine improved paroxysmal dyskinesia caused by the PRRT2 mutation.
000B61 (2012)	Edoardo Ferlazzo ; Sara Gasparini ; Antonio Gambardella ; Angelo Labate ; Vittoria Cianci ; Andrea Cherubini ; Pierluigi Lanza ; Aldo Quattrone ; Umberto Aguglia	Unilateral basal ganglia atrophy in a patient with tuberous sclerosis complex and hemichorea.
001477 (2011)	Kailash P. Bhatia [Royaume-Uni]	Paroxysmal dyskinesias
001668 (2011)	Melissa J. Armstrong [Canada] ; Binit B. Shah [Canada] ; Robert Chen [Canada] ; Michael J. Angel [Canada] ; Anthony E. Lang [Canada]	Expanding the phenomenology of benign hereditary chorea: Evolution from chorea to myoclonus and dystonia
001813 (2011)	Martina Wolf [Allemagne] ; Andreas Bruehschwein [Allemagne] ; Carola Sauter-Louis [Allemagne] ; Adrian C. Sewell [Allemagne] ; Andrea Fischer [Allemagne]	An inherited episodic head tremor syndrome in Doberman pinscher dogs
001E00 (2010)	Kyoko Kanazawa [Japon] ; Satoko Kumada [Japon] ; Mitsuhiro Kato [Japon] ; Hirotomo Saitsu [Japon] ; Eiji Kurihara [Japon] ; Naomichi Matsumoto [Japon]	Choreo–ballistic movements in a case carrying a missense mutation in syntaxin binding protein 1 gene
001E32 (2010)	Elena Salvatore [Italie] ; Luigi Di Maio [Italie] ; Alessandro Filla [Italie] ; Alfonso M. Ferrara [Italie] ; Carlo Rinaldi [Italie] ; Francesco Saccà [Italie] ; Silvio Peluso [Italie] ; Paolo E. Macchia [Italie] ; Sabina Pappatà [Italie] ; Giuseppe De Michele [Italie]	Benign hereditary chorea: Clinical and neuroimaging features in an Italian family
002038 (2009)	Gabor G. Kovacs [Autriche, États-Unis, Hongrie] ; Jill R. Murrell [États-Unis] ; Sandor Horvath [Hongrie] ; Laszlo Haraszti [Hongrie] ; Katalin Majtenyi [Hongrie] ; Maria J. Molnar [Hongrie] ; Herbert Budka [Autriche] ; Bernardino Ghetti [États-Unis] ; Salvatore Spina [États-Unis, Italie]	TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea
002093 (2009)	André R. Troiano [France] ; Paulo C. Trevisol-Bittencourt [Brésil]	Re: Chorea‐acanthocytosis: Report of two Brazilian cases
002664 (2008)	Amir Glik [Israël] ; Isabelle Vuillaume [France] ; David Devos [France] ; Rivka Inzelberg [Israël]	Psychosis, short stature in benign hereditary chorea: A novel thyroid transcription factor‐1 mutation
002702 (2008)	Thomas L. Shirley [États-Unis] ; Lekha M. Rao [États-Unis] ; Ellen J. Hess [États-Unis] ; H. A. Jinnah [États-Unis]	Paroxysmal dyskinesias in mice
002A33 (2008)	Muhammad U. Farooq [États-Unis] ; Susan V. Balmer [États-Unis] ; Steven T. Deroos [États-Unis] ; Karen L. Houtman [États-Unis] ; Kipp L. Chillag [États-Unis]	A novel mutation in the iduronate 2 sulfatase gene resulting in mucopolysaccharidosis type II and chorea: Case report of two siblings
002C50 (2007)	Shinji Saiki [Japon] ; Koichiro Sakai [Japon] ; Ken-Ya Murata [Japon] ; Misuzu Saiki [Japon] ; Megumi Nakanishi [Japon] ; Yoko Kitagawa [Japon] ; Muichi Kaito [Japon] ; Yuichiro Gondo [Japon] ; Toshihide Kumamoto [Japon] ; Makoto Matsui [Japon] ; Nobutaka Hattori [Japon] ; Genjiro Hirose [Japon]	Primary skeletal muscle involvement in chorea‐acanthocytosis
002C73 (2007)	Ruth H. Walker [États-Unis] ; Hans H. Jung [Suisse] ; François Tison [France] ; Soohee Lee [États-Unis] ; Adrian Danek [Allemagne]	Phenotypic variation among brothers with the McLeod neuroacanthocytosis syndrome
002C74 (2007)	Marcelo Miranda [Chili] ; Claudia Castiglioni [Chili] ; Beat M. Frey [Suisse] ; Martin Hergersberg [Suisse] ; Adrian Danek [Allemagne] ; Hans H. Jung [Suisse]	Phenotypic variability of a distinct deletion in McLeod syndrome
002F55 (2007)	Friedrich Asmus [Allemagne] ; Anita Devlin [Royaume-Uni] ; Marita Munz [Allemagne] ; Alexander Zimprich [Autriche] ; Thomas Gasser [Allemagne] ; Patrick F. Chinnery [Royaume-Uni]	Clinical differentiation of genetically proven benign hereditary chorea and myoclonus‐dystonia
002F91 (2007)	Galit Kleiner-Fisman [Canada] ; Anthony E. Lang [Canada]	Benign hereditary chorea revisited: A journey to understanding

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