Literature DB >> 23684369

Screening for progranulin mutations by serum protein dosage in common neurodegenerative disorders.

Eloy Rodríguez-Rodríguez, José Luis Vázquez-Higuera, Pascual Sánchez-Juan, Isabel González-Aramburu, Ana Pozueta, Ignacio Mateo, Miguel Calero, José Luis Dobato, Jon Infante, José Berciano, Onofre Combarros.   

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Year:  2013        PMID: 23684369     DOI: 10.1016/j.parkreldis.2013.04.008

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


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  1 in total

Review 1.  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

  1 in total

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