Genetic heterogeneity in patients with pantothenate kinase–associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern-Reference-Cited by-同舟云学术

Genetic heterogeneity in patients with pantothenate kinase–associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern

Published:2006 Issue:2 Volume:21 Page:252-254
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Valentino Paola,Annesi Grazia,Cirò Candiano Innocenza C.,Annesi Ferdinanda,Civitelli Donatella,Tarantino Patrizia,Naso Francesco,Spadafora Patrizia,Carrideo Sara,De Marco Elvira V.,Consoli Domenico,Zappia Mario,Gambardella Antonio,Quattrone Aldo

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference5 articles.

1. Hallervorden-Spatz Syndrome

2. Homozygosity mapping of Hallervorden–Spatz syndrome to chromosome 20p12.3–p13

3. A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome

4. Genetic, Clinical, and Radiographic Delineation of Hallervorden–Spatz Syndrome

5. Clinical heterogeneity of neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome) and pantothenate kinase-associated neurodegeneration

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1. Dystonia;Principles and Practice of Movement Disorders;2021

2. Atypical pantothenate kinase-associated neurodegeneration: Clinical description of two brothers and a review of the literature;Revue Neurologique;2017-12

3. Mutational analysis of COASY in an Italian patient with NBIA;Parkinsonism & Related Disorders;2016-07

4. Late Onset Atypical Pantothenate-Kinase-Associated Neurodegeneration;Case Reports in Neurological Medicine;2013

5. A Case of Retinal Pigmentary Degeneration in PKAN;Journal of the Korean Ophthalmological Society;2013