Literature DB >> 26868161

Early-onset Parkinson disease leading to diagnosis of 22q11.2 deletion syndrome.

Rebecca Pollard1, Markus Hannan1, Jody Tanabe2, Brian D Berman3.   

Abstract

Entities:  

Keywords:  22q11.2 deletion syndrome; DiGeorge syndrome; Early-onset; Parkinson disease

Mesh：

Year:  2016        PMID： 26868161     DOI： 10.1016/j.parkreldis.2016.01.027

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


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  4 in total

1.  Parkinson's disease with hypocalcaemia: adult presentation of 22q11.2 deletion syndrome.

Authors:  Fradique Moreira; Ana Brás; Joana Ramos Lopes; Cristina Januário
Journal:  BMJ Case Rep       Date:  2018-03-22

Review 2.  New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

Authors:  Andreas Puschmann
Journal:  Curr Neurol Neurosci Rep       Date:  2017-09       Impact factor: 5.081

3.  Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease.

Authors:  Nancy J Butcher; Daniele Merico; Mehdi Zarrei; Lucas Ogura; Christian R Marshall; Eva W C Chow; Anthony E Lang; Stephen W Scherer; Anne S Bassett
Journal:  PLoS One       Date:  2017-04-21       Impact factor: 3.240

4.  Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease.

Authors:  Stefano Gambardella; Rosangela Ferese; Simona Scala; Stefania Carboni; Francesca Biagioni; Emiliano Giardina; Stefania Zampatti; Nicola Modugno; Francesco Fabbiano; Francesco Fornai; Diego Centonze; Stefano Ruggieri
Journal:  Parkinsons Dis       Date:  2018-06-21
  4 in total

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