Newborn screening for X-linked adrenoleukodystrophy: evidence summary and advisory committee recommendation-Reference-Cited by-同舟云学术

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Newborn screening for X-linked adrenoleukodystrophy: evidence summary and advisory committee recommendation

Published:2017-01 Issue:1 Volume:19 Page:121-126
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Kemper Alex R.,Brosco Jeffrey,Comeau Anne Marie,Green Nancy S.,Grosse Scott D.,Jones Elizabeth,Kwon Jennifer M.,Lam Wendy K.K.,Ojodu Jelili,Prosser Lisa A.,Tanksley Susan

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim201668.pdf

Reference32 articles.

Cited by 75 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. Adrenal insufficiency and the use of mineralocorticoid treatment in male patients with adrenoleukodystrophy; a retrospective analysis of an institutional database;BMC Endocrine Disorders;2024-09-09

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

3. A pilot study of newborn screening for X-linked adrenoleukodystrophy based on liquid chromatography-tandem mass spectrometry method for detection of C26:0-lysophosphatidylcholine in dried blood spots: Results from 43,653 newborns in a southern Chinese population;Clinica Chimica Acta;2024-01

4. Hematopoietic stem cell therapy and ex vivo gene therapy for X-linked adrenoleukodystrophy;Handbook of Clinical Neurology;2024

5. Newborn screening for adrenoleukodystrophy: International experiences and challenges;Molecular Genetics and Metabolism;2023-12

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