Literature DB >> 20171924

Screening for MAPT and PGRN mutations in Korean patients with PSP/CBS/FTD.

Han-Joon Kim, Beom S Jeon, Ji Young Yun, Moon-Woo Seong, Sung Sup Park, Jee-Young Lee.   

Abstract

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20171924     DOI: 10.1016/j.parkreldis.2010.01.004

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


× No keyword cloud information.
  6 in total

1.  Identification of Parkinson's disease candidate genes using CAESAR and screening of MAPT and SNCAIP in South African Parkinson's disease patients.

Authors:  Rowena J Keyser; Ekow Oppon; Jonathan A Carr; Soraya Bardien
Journal:  J Neural Transm (Vienna)       Date:  2011-02-23       Impact factor: 3.575

Review 2.  Tau and MAPT genetics in tauopathies and synucleinopathies.

Authors:  Etienne Leveille; Owen A Ross; Ziv Gan-Or
Journal:  Parkinsonism Relat Disord       Date:  2021-09-14       Impact factor: 4.402

3.  Microtubule-associated protein tau genetic variations are uncommon cause of frontotemporal dementia in south India.

Authors:  P M Aswathy; P S Jairani; Joe Verghese; Srinivas Gopala; P S Mathuranath
Journal:  Neurobiol Aging       Date:  2013-09-13       Impact factor: 4.673

Review 4.  A network of RNA and protein interactions in Fronto Temporal Dementia.

Authors:  Francesca Fontana; Kavitha Siva; Michela A Denti
Journal:  Front Mol Neurosci       Date:  2015-03-19       Impact factor: 5.639

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

Review 6.  Genetics of Progressive Supranuclear Palsy.

Authors:  Sun Young Im; Young Eun Kim; Yun Joong Kim
Journal:  J Mov Disord       Date:  2015-09-10
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.