Clinical Heterogeneity of Atypical Pantothenate Kinase-Associated Neurodegeneration in Koreans-Reference-Cited by-同舟云学术

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Clinical Heterogeneity of Atypical Pantothenate Kinase-Associated Neurodegeneration in Koreans

Published:2016-01-25 Issue:1 Volume:9 Page:20-27
ISSN:2005-940X
Container-title:Journal of Movement Disorders
language:en
Short-container-title:JMD

Author:

Lee Jae-Hyeok,Park Jongkyu,Ryu Ho-Sung,Park Hyeyoung,Kim Young Eun,Hong Jin Yong,Nam Sang Ook,Sung Young-Hee,Lee Seung-Hwan,Lee Jee-Young,Lee Myung Jun,Kim Tae-Hyoung,Lyoo Chul Hyoung,Chung Sun Ju,Koh Seong Beom,Lee Phil Hyu,Cho Jin Whan,Park Mee Young,Kim Yun Joong,Sohn Young H.,Jeon Beom Seok,Lee Myung Sik

Funder

Ministry of Education, Science and Technology

Pusan National University Yangsan Hospital

Publisher

The Korean Movement Disorder Society

Subject

Neurology (clinical),Neurology

Link

http://e-jmd.org/upload/jmd-15058.pdf

Reference33 articles.

1. Neurodegeneration with Brain Iron Accumulation: Diagnosis and Management

2. Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories

3. Neurodegenerations with Brain Iron Accumulation

4. Current Concepts and Controversies in Neurodegeneration with Brain Iron Accumulation

5. The diverse phenotype and genotype of pantothenate kinase-associated neurodegeneration

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1. Unusual Movement Disorders;Movement Disorders Phenomenology;2024

2. The first Vietnamese patient who presented late onset of pantothenate kinase-associated neurodegeneration diagnosed by whole exome sequencing: A case report;Medicine;2023-10-27

3. Typical pantothenate kinase-associated neurodegeneration caused by compound heterozygous mutations in PANK2 gene in a Chinese patient: a case report and literature review;Frontiers in Neurology;2023-04-28

4. Long-Term Outcomes of Deep Brain Stimulation in Pantothenate Kinase-Associated Neurodegeneration-Related Dystonia;Journal of Movement Disorders;2022-09-30

5. Genetic mutation spectrum of pantothenate kinase-associated neurodegeneration expanded by breakpoint sequencing in pantothenate kinase 2 gene;Orphanet Journal of Rare Diseases;2022-03-04

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