Prenatal Diagnosis of Metachromatic Leukodystrophy in a Family with Pseudo Arylsulfatase A Deficiency by the Cerebroside Sulfate Loading Test-Reference-Cited by-同舟云学术

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Prenatal Diagnosis of Metachromatic Leukodystrophy in a Family with Pseudo Arylsulfatase A Deficiency by the Cerebroside Sulfate Loading Test

Published:1980-03 Issue:3 Volume:14 Page:224-227
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Kihara Hayato,Ho Chen-Kung,Fluharty Arvan L,Tsay Katherine K,Hartlage Patricia L

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Cited by 78 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. Extremely low arylsulfatase A enzyme activity does not necessarily cause symptoms: A long‐term follow‐up and review of the literature;JIMD Reports;2022-05-04

2. Metachromatic Leukodystrophy: Diagnosis, Modeling, and Treatment Approaches;Frontiers in Medicine;2020-10-20

3. New therapeutic strategies for the treatment of metachromatic leukodystrophy;Genes & Cells;2020-06-15

4. Tandem Mass Spectrometry of Sphingolipids;Advances in Clinical Chemistry;2016

5. Direct tandem mass spectrometric profiling of sulfatides in dry urinary samples for screening of metachromatic leukodystrophy;Clinica Chimica Acta;2013-10

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