Movement Disorders (revue) - Exploration (Accueil)

Index « Mesh.i » - entrée « Intellectual Disability »
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Inteins < Intellectual Disability < Intelligence  Facettes :

List of bibliographic references indexed by Intellectual Disability

Number of relevant bibliographic references: 24.
[0-20] [0 - 20][0 - 24][20-23][20-40]
Ident.Authors (with country if any)Title
000005 (2015) Andrew Singleton [États-Unis]X-linked Parkinson's disease.
000354 (2015) Janel O. Johnson [Royaume-Uni] ; Giovanni Stevanin ; Joyce Van De Leemput ; Dena G. Hernandez ; Sampath Arepalli ; Sylvie Forlani ; Reza Zonozi ; J Raphael Gibbs ; Alexis Brice ; Alexandra Durr ; Andrew B. SingletonA 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome.
000494 (2014) Geetanjali S. Rathore [États-Unis] ; Christian P. Schaaf ; Amber J. StoccoNovel mutation of the WDR45 gene causing beta-propeller protein-associated neurodegeneration.
000727 (2013) Maja Kojovic [Royaume-Uni] ; Isabel Pareés ; Tania Lampreia ; Karolina Pienczk-Reclawowicz ; Georgia Xiromerisiou ; Ignacio Rubio-Agusti ; Milica Kramberger ; Miryam Carecchio ; Anas M. Alazami ; Francesco Brancati ; Jaroslaw Slawek ; Zvezdan Pirtosek ; Enza Maria Valente ; Fowzan S. Alkuraya ; Mark J. Edwards ; Kailash P. BhatiaThe syndrome of deafness-dystonia: clinical and genetic heterogeneity.
000822 (2013) Laura Cif [France] ; Victoria Gonzalez ; Sara Garcia-Ptacek ; Syril James ; Julien Boetto ; Anne Seychelles ; Thomas Roujeau ; Ana Maria Moura De Ribeiro ; Martine Sillon ; Michel Mondain ; Philippe CoubesProgressive dystonia in Mohr-Tranebjaerg syndrome with cochlear implant and deep brain stimulation.
000A52 (2013) Thomas Foltynie [Royaume-Uni]Commentary.
000A95 (2013) Darius Ebrahimi-Fakhari [Allemagne]Autophagy and neurodegeneration - genetic findings in SENDA syndrome, a subtype of neurodegeneration with brain iron accumulation, provide a novel link.
000B76 (2012) Ainhi D. Ha [Australie] ; Kaitlyn L. Parratt ; Nanna D. Rendtorff ; Marianne Lodahl ; Karl Ng ; Dominic B. Rowe ; Carolyn M. Sue ; Michael W. Hayes ; Lisbeth Tranebjaerg ; Victor S C. FungThe phenotypic spectrum of dystonia in Mohr-Tranebjaerg syndrome.
001A00 (2010) P. David Charles [États-Unis] ; Chandler E. Gill [États-Unis] ; Henry M. Taylor [États-Unis] ; Michael S. Putman [États-Unis] ; Caralee R. Blair [États-Unis] ; Amanda G. Roberts [États-Unis] ; Gregory D. Ayers [États-Unis] ; Peter E. Konrad [États-Unis]Spasticity treatment facilitates direct care delivery for adults with profound intellectual disability
002835 (2008) Susanne A. Schneider [Royaume-Uni] ; Mary M. Robertson [Royaume-Uni] ; Renata Rizzo [Italie] ; Jeremy Turk [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Michael Orth [Royaume-Uni, Allemagne]Fragile X syndrome associated with tic disorders
002890 (2008) Susanne A. Schneider [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]Dystonia in the Woodhouse Sakati syndrome: A new family and literature review
002E83 (2007) Eiichiro Nagata [Japon] ; Arifumi Kosakai [Japon] ; Kortaro Tanaka [Japon] ; Masaya Segawa [Japon] ; Hiroki Fujioka [Japon] ; Haruo Shintaku [Japon] ; Norihiro Suzuki [Japon]Dopa‐responsive dystonia (Segawa disease)‐like disease accompanied by mental retardation: A case report
003472 (2006) Kana Tojo [Japon] ; Yoshiki Sekijima [Japon] ; Tamio Suzuki [Japon] ; Noriyuki Suzuki [Japon] ; Yasushi Tomita [Japon] ; Kunihiro Yoshida [Japon] ; Takao Hashimoto [Japon] ; Shu-Ichi Ikeda [Japon]Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation
003D71 (2004) Uday Muthane [Inde] ; Yasha Chickabasaviah [Inde] ; Chris Kaneski [États-Unis] ; Susurla K. Shankar [Inde] ; Gayathri Narayanappa [Inde] ; Rita Christopher [Inde] ; Srikanth Subbamma Govindappa [Inde]Clinical features of adult GM1 gangliosidosis: Report of three Indian patients and review of 40 cases
004803 (2001) T. Perniola [Italie] ; L. Margari [Italie] ; M. G. De Iaco [Italie] ; A. Presicci [Italie] ; P. Ventura [Italie] ; E. Ferrannini [Italie] ; G. Illiceto [Italie]Familial paroxysmal exercise‐induced dyskinesia, epilepsy, and mental retardation in a family with autosomal dominant inheritance
005242 (1997) Adrian Tan [États-Unis] ; Miran Salgado [États-Unis] ; Fahn [États-Unis]The characterization and outcome of stereotypic movements in nonautistic children
005305 (1997) Factor [États-Unis] ; Kevin D. Barron [États-Unis]Mosaic pattern of gliosis in the neostriatum of a north american man with craniocervical dystonia and parkinsonism
005912 (1995) Gordon [États-Unis] ; Susan Bressman [États-Unis] ; Mitchell F. Brin [États-Unis] ; Deborah De Leon [États-Unis] ; Dorothy Warburton [États-Unis] ; Kwame Yeboa [États-Unis] ; Stanley Fahn [États-Unis]Dystonia in a patient with deletion of 18q
005B24 (1994) A. Rossi [Italie] ; B. Decchi [Italie] ; D. Grossi [Italie]On the nature of motor disorders in mentally retarded patients
005B64 (1994) Andermann [Canada] ; Shunsuke Ohtahara [Japon] ; Eva Andermann [Canada] ; Peter Camfield [Canada] ; Katsuhiro Kobayashi [Japon]Infantile hypotonia and paroxysmal dystonia: A variant of alternating hemiplegia of childhood?
005B90 (1994) Kyllerman [Suède] ; O. H. Skjeldal [Norvège] ; M. Lundberg [Suède] ; I. Holme [Suède] ; E. Jellum [Norvège] ; U. Von Döbeln [Suède] ; A. Fossen [Norvège] ; G. Carlsson [Suède]Dystonia and dyskinesia in glutaric aciduria type I: Clinical heterogeneity and therapeutic considerations

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