Literature DB >> 21183274

Heterozygous exon 3 deletion in the Parkin gene in a patient with clinical and radiological MSA-C phenotype.

Orlando Graziani Povoas Barsottini1, André Carvalho Felício, Patrícia de Carvalho Aguiar, Clécio Godeiro-Junior, Jose Luiz Pedroso, Camila Catherine Henriques de Aquino, Edson Bor-Seng-Shu, Luiz Augusto Franco de Andrade.   

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Year:  2010        PMID： 21183274     DOI： 10.1016/j.clineuro.2010.11.015

Source DB:  PubMed          Journal:  Clin Neurol Neurosurg        ISSN： 0303-8467            Impact factor:   1.876


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  2 in total

1.  Mutations in PRKN and SNCA Genes Important for the Progress of Parkinson's Disease.

Authors:  Anna Oczkowska; Wojciech Kozubski; Margarita Lianeri; Jolanta Dorszewska
Journal:  Curr Genomics       Date:  2013-12       Impact factor: 2.236

2.  Dopamine transporter imaging using 99mTc-TRODAT-1 SPECT in Parkinson's disease.

Authors:  Edson Bor-Seng-Shu; Andre C Felicio; Pedro Braga-Neto; Ilza Rosa Batista; Wellingson Silva Paiva; Daniel Ciampi de Andrade; Manoel Jacobsen Teixeira; Luis Augusto Franco de Andrade; Orlando Graziani Povoas Barsottini; Ming Chi Shih; Rodrigo A Bressan; Henrique Ballalai Ferraz
Journal:  Med Sci Monit       Date:  2014-08-11
  2 in total

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