Genetic, clinical, and imaging characterization of one patient with late-onset, slowly progressive, pantothenate kinase-associated neurodegeneration-Reference-Cited by-同舟云学术

Genetic, clinical, and imaging characterization of one patient with late-onset, slowly progressive, pantothenate kinase-associated neurodegeneration

Published:2005-11-02 Issue:3 Volume:21 Page:417-418
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Antonini Angelo,Goldwurm Stefano,Benti Riccardo,Prokisch Holger,Ebhardt Monika,Cilia Roberto,Zini Michela,Righini Andrea,Cossu Giovanni,Pezzoli Gianni

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference8 articles.

1. A novel pantothenate kinase gene is defective in Hallervorden-Spatz syndrome;Zhou;Nat Genet,2001

2. An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondria;Hortnagel;Hum Mol Genet,2003

3. Clinical heterogeneity of neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome) and pantothenate kinase-associated neurodegeneration;Thomas;Mov Disord,2004

4. PET and SPECT functional imaging in Parkinson's disease;Antonini;Sleep Med,2004

5. Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome;Hayflick;N Engl J Med,2003

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