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Review

Developing therapeutic approaches for metachromatic leukodystrophy

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Pages 729-745 | Published online: 08 Aug 2013

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Chueh Lin Hsu, Piotr Iwanowski, Chueh Hsuan Hsu & Wojciech Kozubski. (2021) Genetic diseases mimicking multiple sclerosis. Postgraduate Medicine 133:7, pages 728-749.
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Articles from other publishers (15)

Bing-lei Wang, Fen-lei Lu, Yu-chen Sun & Hui-juan Wang. (2022) Case report: A compound heterozygous mutations in ARSA associated with adult-onset metachromatic leukodystrophy. Frontiers in Neurology 13.
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F. Eichler, Caroline Sevin, M. Barth, F. Pang, K. Howie, M. Walz, A. Wilds, C. Calcagni, C. Chanson & L. Campbell. (2022) Understanding caregiver descriptions of initial signs and symptoms to improve diagnosis of metachromatic leukodystrophy. Orphanet Journal of Rare Diseases 17:1.
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Bronwyn Boyes. (2022) Implications of the First Ex Vivo Gene Therapy Approved for Treating Early-Onset Metachromatic Leukodystrophy. EMJ Neurology, pages 20-28.
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Joseph C. Nowacki, Ashley M. Fields & Meng Meng Fu. (2022) Emerging cellular themes in leukodystrophies. Frontiers in Cell and Developmental Biology 10.
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Aslı BOLAYIR. (2022) Aralıksız psödobulber ağlama atakları ile başvuran geç juvenil başlangıçlı bir metakromatik lökodistrofi olgusu. Cumhuriyet Medical Journal.
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Nayibe Tatiana Sanchez-AlvarezPaula Katherine Bautista-NiñoJuanita Trejos-Suárez & Norma Cecilia Serrano-Diaz. (2021) Metachromatic Leukodystrophy: Diagnosis and Treatment Challenges. Bionatura 3:3, pages 2083-2090.
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Mariola J. Edelmann & Gustavo H. B. Maegawa. (2020) CNS-Targeting Therapies for Lysosomal Storage Diseases: Current Advances and Challenges. Frontiers in Molecular Biosciences 7.
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Alisa A. Shaimardanova, Daria S. Chulpanova, Valeriya V. Solovyeva, Aysilu I. Mullagulova, Kristina V. Kitaeva, Cinzia Allegrucci & Albert A. Rizvanov. (2020) Metachromatic Leukodystrophy: Diagnosis, Modeling, and Treatment Approaches. Frontiers in Medicine 7.
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Sukanthini Thurairatnam, Sungtaek Lim, Robert H. BarkerJr.Jr., Yong Mi Choi-Sledeski, Bradford H. Hirth, John Jiang, John E. Macor, Elina Makino, Sachin Maniar, Kwon Musick, James R. Pribish & Mark Munson. (2020) Brain Penetrable Inhibitors of Ceramide Galactosyltransferase for the Treatment of Lysosomal Storage Disorders. ACS Medicinal Chemistry Letters 11:10, pages 2010-2016.
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Efthalia Angelopoulou, Yam Nath Paudel, Chiara Villa & Christina Piperi. (2020) Arylsulfatase A (ASA) in Parkinson’s Disease: From Pathogenesis to Biomarker Potential. Brain Sciences 10:10, pages 713.
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Anna Kloska, Magdalena Węsierska, Marcelina Malinowska, Magdalena Gabig-Cimińska & Joanna Jakóbkiewicz-Banecka. (2020) Lipophagy and Lipolysis Status in Lipid Storage and Lipid Metabolism Diseases. International Journal of Molecular Sciences 21:17, pages 6113.
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Jacob M. Favret, Nadav I. Weinstock, M. Laura Feltri & Daesung Shin. (2020) Pre-clinical Mouse Models of Neurodegenerative Lysosomal Storage Diseases. Frontiers in Molecular Biosciences 7.
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Li Chen, Huifang Yan, Binbin Cao, Ye Wu, Qiang Gu, Jiangxi Xiao, Yanling Yang, Huixia Yang, Zhen Shi, Zhixian Yang, Hong Pan, Xingzhi Chang, Junya Chen, Yu Sun, Yuehua Zhang, Xiru Wu, Yuwu Jiang & Jingmin Wang. (2018) Identification of Novel ARSA Mutations in Chinese Patients with Metachromatic Leukodystrophy . International Journal of Genomics 2018, pages 1-9.
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Rajul Rastogi. (2016) MRI Diagnosis in Classical Metachromatic Leukodystrophy. International Journal of Neurology and Brain Disorders 4:1, pages 1-3.
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Klaas Arts. (2015) Secundaire psychosen bij behandelbare neurologische aandoeningen. Tijdschrift voor Neuropsychiatrie en Gedragsneurologie 3:1, pages 17-29.
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