Literature DB >> 15032978

Cerebellar ataxia as atypical manifestation of the 3243A>G MELAS mutation.

V Petruzzella, S Zoccolella, A Amati, A Torraco, P Lamberti, F Carnicella, L Serlenga, S Papa.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2004        PMID： 15032978     DOI： 10.1111/j..2004.00185.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


× No keyword cloud information.
  3 in total

Review 1.  Cerebral imaging in paediatric mitochondrial disorders.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  Neuroradiol J       Date:  2018-07-06

2.  Brain anomalies in maternally inherited diabetes and deafness syndrome.

Authors:  I Fromont; F Nicoli; R Valéro; O Felician; B Lebail; Y Lefur; J Mancini; V Paquis-Flucklinger; P J Cozzone; Bernard Vialettes
Journal:  J Neurol       Date:  2009-06-18       Impact factor: 4.849

3.  Familial Pernicious Chronic Intestinal Pseudo-obstruction with a Mitochondrial DNA A3243G Mutation.

Authors:  Junichiro Suzuki; Mai Iwata; Hideyuki Moriyoshi; Suguru Nishida; Takeshi Yasuda; Yasuhiro Ito
Journal:  Intern Med       Date:  2017-05-01       Impact factor: 1.271
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.