Literature DB >> 33046383

Untangling the complicated web of ATP1A3 mutations.

Philippe Salles1, Hubert H Fernandez2.   

Abstract

Entities:  

Year:  2020        PMID： 33046383     DOI： 10.1016/j.parkreldis.2020.09.010

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


× No keyword cloud information.
  3 in total

1.  Long-Term Follow-Up of a Patient with a De Novo p.Arg769Cys Mutation in the ATP1A3 Gene.

Authors:  Anjali Chouksey; Asish Vijayaraghavan; Sony Mohan; Srija Inturi; A T Prabhakar; Vivek Mathew
Journal:  Mov Disord Clin Pract       Date:  2021-09-10

Review 2.  ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum.

Authors:  Philippe A Salles; Ignacio F Mata; Tobias Brünger; Dennis Lal; Hubert H Fernandez
Journal:  Front Neurol       Date:  2021-04-01       Impact factor: 4.003

Review 3.  The Phenotypic Continuum of ATP1A3-Related Disorders.

Authors:  Aikaterini Vezyroglou; Rhoda Akilapa; Katy Barwick; Saskia Koene; Catherine A Brownstein; Muriel Holder-Espinasse; Andrew E Fry; Andrea H Németh; George K Tofaris; Eleanor Hay; Imelda Hughes; Sahar Mansour; Santosh R Mordekar; Miranda Splitt; Peter D Turnpenny; Demetria Demetriou; Tamara T Koopmann; Claudia A L Ruivenkamp; Pankaj B Agrawal; Lucinda Carr; Virginia Clowes; Neeti Ghali; Susan Elizabeth Holder; Jessica Radley; Alison Male; Sanjay M Sisodiya; Manju A Kurian; J Helen Cross; Meena Balasubramanian
Journal:  Neurology       Date:  2022-07-18       Impact factor: 11.800
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.