Literature DB >> 34606069

Late onset Aicardi-Goutières syndrome case report: a rare white matter disease mimicking as pseudo-enzyme deficiency.

Melis Ulak Ozkan1, Selahattin Katar1, Edibe Pembegul Yildiz2,3, Nur Aydinli1, Mine Caliskan1,4.   

Abstract

Entities:  

Mesh：

Year:  2021        PMID： 34606069     DOI： 10.1007/s13760-021-01809-9

Source DB:  PubMed          Journal:  Acta Neurol Belg        ISSN： 0300-9009            Impact factor:   2.396


× No keyword cloud information.
  2 in total

1.  Arylsulfatase A pseudodeficiency incidence in Turkey.

Authors:  S Emre; M Topçu; M Terzioğlu; Y Renda
Journal:  Turk J Pediatr       Date:  2000 Apr-Jun       Impact factor: 0.552

2.  Late-Onset Aicardi-Goutières Syndrome: A Characterization of Presenting Clinical Features.

Authors:  Cara Piccoli; Nowa Bronner; Francesco Gavazzi; Holly Dubbs; Micaela De Simone; Valentina De Giorgis; Simona Orcesi; Elisa Fazzi; Jessica Galli; Silvia Masnada; Davide Tonduti; Costanza Varesio; Adeline Vanderver; Arastoo Vossough; Laura Adang
Journal:  Pediatr Neurol       Date:  2020-11-02       Impact factor: 3.372
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.