Leukoencephalopathies Associated with Disorders of Cobalamin and Folate Metabolism
Author:
Affiliation:
1. Discipline of Paediatrics, University of Sydney, Sydney, Australia
2. Department of Biochemical Genetics and Newborn Screening, The Children's Hospital at Westmead, Westmead, New South Wales, Australia
Publisher
Georg Thieme Verlag KG
Subject
Neurology (clinical),Neurology
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0032-1306389.pdf
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2. Reversible leukoencephalopathy and cerebral atrophy in homocystinuria due to MTHFR deficiency: A treatable metabolic disorder;Journal of Inherited Metabolic Disease;2021-09-28
3. Clinical, biochemical, radiological, and genetic profile of patients with homocysteine remethylation pathway defect and spastic paraplegia;Annals of Indian Academy of Neurology;2021
4. Inborn errors of immunity and metabolic disorders: current understanding, diagnosis, and treatment approaches;Journal of Pediatric Endocrinology and Metabolism;2020-12-16
5. Adulthood leukodystrophies;Nature Reviews Neurology;2018-01-05
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