Clinical and Genetic Aspects of X-Linked Adrenoleukodystrophy-Reference-Cited by-同舟云学术

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Clinical and Genetic Aspects of X-Linked Adrenoleukodystrophy

Published:1998-02 Issue:01 Volume:29 Page:3-13
ISSN:0174-304X
Container-title:Neuropediatrics
language:en
Short-container-title:Neuropediatrics

Author:

Gärtner Jutta,Braun A.,Holzinger A.,Roerig P.,Lenard H.-G.,Roscher A.

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2007-973526.pdf

Cited by 41 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. Bálint syndrome as the presenting manifestation of adrenoleukodystrophy;Neurology Perspectives;2023-04

3. iBRET Screen of the ABCD1 Peroxisomal Network and Mutation-Induced Network Perturbations;Journal of Proteome Research;2021-08-12

4. Identification of a New Fatty Acid Synthesis-Transport Machinery at the Peroxisomal Membrane;Journal of Biological Chemistry;2012-01

5. Genetic variants of methionine metabolism and X-ALD phenotype generation: results of a new study sample;Journal of Neurology;2009-04-08

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