Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia-Reference-Cited by-同舟云学术

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Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia

Published:2019-08 Issue: Volume:65 Page:256-260
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Chen Yi-Jun,Wang Meng-Wen,Dong En-Lin,Lin Xiao-Hong,Wang Ning,Zhang Zai-Qiang,Lin Xiang,Chen Wan-Jin

Funder

National Natural Science Foundation of China

scientific research of Fujian Medical University

Natural Science Foundation of Fujian Province

Joint Funds for the Innovation of Science and Technology of Fujian Province

National Key Clinical Specialty Discipline Construction Program

Key Clinical Specialty Discipline Construction Program of Fujian

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference12 articles.

1. Clinical diagnosis, biochemical findings and MRI spectrum of peroxisomal disorders;Poll-The;Biochim. Biophys. Acta,2012

2. X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management;Engelen;Orphanet J. Rare Dis.,2012

3. Leukodystrophies underlying cryptic spastic paraparesis: frequency and phenotype in 76 patients;Müller vom Hagen;Eur. J. Neurol.,2014

4. X-linked adrenoleukodystrophy in women: a cross-sectional cohort study;Engelen;Brain,2014

5. Quantitative MRI of the spinal cord and brain in adrenomyeloneuropathy: in vivo assessment of structural changes;Castellano;Brain,2016

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A novel ABCD1 gene mutation causes adrenomyeloneuropathy presenting with spastic paraplegia: A case report;Medicine;2024-04-19

2. SPG11: clinical and genetic features of seven Czech patients and literature review;Neurological Research;2022-03-07

3. Clinical, neuroradiological, and molecular characterization of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations: a case series;neurogenetics;2022-02-02

4. Typical and atypical phenotype and neuroimaging of X-linked adrenoleukodystrophy in a Chinese cohort;Neurological Sciences;2022-01-08

5. Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype;Parkinsonism & Related Disorders;2021-11

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