Molecular Basis of Different Forms of Metachromatic Leukodystrophy-Reference-Cited by-同舟云学术

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Molecular Basis of Different Forms of Metachromatic Leukodystrophy

Published:1991-01-03 Issue:1 Volume:324 Page:18-22
ISSN:0028-4793
Container-title:New England Journal of Medicine
language:en
Short-container-title:N Engl J Med

Author:

Polten Andreas,Fluharty Arvan L.,Fluharty Claire B.,Kappler Joachim,von Figura Kurt,Gieselmann Volkmar

Publisher

Massachusetts Medical Society

Subject

General Medicine

Link

http://www.nejm.org/doi/pdf/10.1056/NEJM199101033240104

Cited by 259 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. Lysosomal storage diseases. Sphingolipidoses – leukodystrophy;Pediatrician (St. Petersburg);2024-05-07

2. Newborn screening in metachromatic leukodystrophy – European consensus-based recommendations on clinical management;European Journal of Paediatric Neurology;2024-03

3. Etiologic Spectrum of Pediatric-Onset Leukodystrophies and Genetic Leukoencephalopathies: The Five-Year Experience of a Tertiary Care Center in Southern India;Pediatric Neurology;2024-03

4. A systematic review on the birth prevalence of metachromatic leukodystrophy;Orphanet Journal of Rare Diseases;2024-02-21

5. Therapeutic Strategies for Lysosomal Storage Diseases by Targeting Glial Cells;Physiology and Function of Glial Cells in Health and Disease;2023-12-18

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