Literature DB >> 11921141

Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene.

Peter P Pramstaller1, Bernhard Kis, Cordula Eskelson, Katja Hedrich, Monika Scherer, Eberhard Schwinger, Xandra O Breakefield, Patricia L Kramer, Laurie J Ozelius, Christine Klein.   

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Year:  2002        PMID： 11921141     DOI： 10.1002/mds.10071

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


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  5 in total

1.  Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern Brazil.

Authors:  Hsin F Chien; Christan F Rohé; Maria D L Costa; Guido J Breedveld; Ben A Oostra; Egberto R Barbosa; Vincenzo Bonifati
Journal:  Neurogenetics       Date:  2005-11-22       Impact factor: 2.660

2.  ParkScreen: a low-cost rapid linkage marker panel for Parkinson's disease.

Authors:  Alessandro De Grandi; Claudia Béu Volpato; Elisa Bedin; Cristian Pattaro; Fabio Marroni; Irene Pichler; Andrew Antony Hicks; Giorgio Casari; Peter Paul Pramstaller
Journal:  J Mol Neurosci       Date:  2009-03-25       Impact factor: 3.444

Review 3.  Twenty years since the discovery of the parkin gene.

Authors:  Nobutaka Hattori; Yoshikuni Mizuno
Journal:  J Neural Transm (Vienna)       Date:  2017-06-15       Impact factor: 3.575

Review 4.  Gene-environment interactions: key to unraveling the mystery of Parkinson's disease.

Authors:  Hui-Ming Gao; Jau-Shyong Hong
Journal:  Prog Neurobiol       Date:  2011-03-23       Impact factor: 11.685

5.  Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype.

Authors:  B F L van Nuenen; M M Weiss; B R Bloem; K Reetz; T van Eimeren; K Lohmann; J Hagenah; P P Pramstaller; F Binkofski; C Klein; H R Siebner
Journal:  Neurology       Date:  2008-11-26       Impact factor: 9.910
  5 in total

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