X-Linked Adrenoleukodystrophy
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Publisher
Springer Singapore
Link
http://link.springer.com/content/pdf/10.1007/978-981-10-7668-8_23
Reference9 articles.
1. Niu YF, Ni W, Wu ZY. ABCD1 mutations and phenotype distribution in Chinese patients with X-linked adrenoleukodystrophy. Gene. 2013;522(1):117–20.
2. Kemp S, Berger J, Aubourg P. X-linked adrenoleukodystrophy: clinical, metabolic, genetic and pathophysiological aspects. Biochim Biophys Acta. 2012;1822(9):1465–74.
3. Chiu HC, Liang JS, Wang JS, Lu JF. Mutational analyses of Taiwanese kindred with X-linked adrenoleukodystrophy. Pediatr Neurol. 2006;35(4):250–6.
4. Cappa M, Bizzarri C, Vollono C, Petroni A, Banni S. Adrenoleukodystrophy. Endocr Dev. 2011;20:149–60.
5. Traboulsi EI, Maumenee IH. Ophthalmologic manifestations of X-linked childhood adrenoleukodystrophy. Ophthalmology. 1987;94(1):47–52.
Cited by 2 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. Optic nerve demyelination as the presenting feature of adrenoleukodystrophy in a child;Indian Journal of Ophthalmology;2022
2. Clinical, neuroimaging, biochemical, and genetic features in six Chinese patients with Adrenomyeloneuropathy;BMC Neurology;2019-09-16
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