Literature DB >> 22109955

G303V tau mutation presenting with progressive supranuclear palsy-like features.

Ariane Choumert, Alice Poisson, Jérôme Honnorat, Isabelle Le Ber, Agnes Camuzat, Emmanuel Broussolle, Stéphane Thobois.   

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Year:  2011        PMID： 22109955     DOI： 10.1002/mds.24060

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


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  6 in total

1.  Three sib-pairs of autopsy-confirmed progressive supranuclear palsy.

Authors:  Shinsuke Fujioka; Monica Y Sanchez Contreras; Audrey J Strongosky; Kotaro Ogaki; Nathaniel Robb Whaley; Pawel M Tacik; Jay A van Gerpen; Ryan J Uitti; Owen A Ross; Zbigniew K Wszolek; Rosa Rademakers; Dennis W Dickson
Journal:  Parkinsonism Relat Disord       Date:  2014-11-15       Impact factor: 4.891

Review 2.  The genetics of dystonias.

Authors:  Mark S LeDoux
Journal:  Adv Genet       Date:  2012       Impact factor: 1.944

3.  Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.

Authors:  Raffaele Ferrari; Mina Ryten; Roberto Simone; Daniah Trabzuni; Nayia Nicolaou; Naiya Nicolaou; Geshanthi Hondhamuni; Adaikalavan Ramasamy; Jana Vandrovcova; Michael E Weale; Andrew J Lees; Parastoo Momeni; John Hardy; Rohan de Silva
Journal:  Neurobiol Aging       Date:  2014-01-13       Impact factor: 4.673

Review 4.  Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.

Authors:  Carmen Gasca-Salas; Mario Masellis; Edwin Khoo; Binit B Shah; David Fisman; Anthony E Lang; Galit Kleiner-Fisman
Journal:  PLoS One       Date:  2016-04-21       Impact factor: 3.240

Review 5.  Genotype-Phenotype Correlation in Progressive Supranuclear Palsy Syndromes: Clinical and Radiological Similarities and Specificities.

Authors:  Iñigo Ruiz-Barrio; Andrea Horta-Barba; Ignacio Illán-Gala; Jaime Kulisevsky; Javier Pagonabarraga
Journal:  Front Neurol       Date:  2022-04-26       Impact factor: 4.086

6.  MAPT as a predisposing gene for sporadic amyotrophic lateral sclerosis in the Chinese Han population.

Authors:  Pu Fang; Wenyuan Xu; Chengsi Wu; Min Zhu; Xiaobing Li; Daojun Hong
Journal:  Neural Regen Res       Date:  2013-11-25       Impact factor: 5.135
  6 in total

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