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23. Globid leukodystrophy. II. Ultrastructure and chemical pathology. Malone MJ; Szöke M; Davis DA Arch Neurol; 1975 Sep; 32(9):613-7. PubMed ID: 1164213 [TBL] [Abstract][Full Text] [Related]
24. Advances and pitfalls of cell therapy in metabolic leukodystrophies. Miranda CO; Brites P; Mendes Sousa M; Teixeira CA Cell Transplant; 2013; 22(2):189-204. PubMed ID: 23006656 [TBL] [Abstract][Full Text] [Related]
25. Metabolism of cerebroside sulfate and subcellular distribution of its metabolites in cultured skin fibroblasts from controls, metachromatic leukodystrophy, and globoid cell leukodystrophy. Inui K; Furukawa M; Okada S; Yabuuchi H J Clin Invest; 1988 Feb; 81(2):310-7. PubMed ID: 3339122 [TBL] [Abstract][Full Text] [Related]
26. Nosology of the leukodystrophies: ultrastructural contributions. Nelson E Birth Defects Orig Artic Ser; 1971 Feb; 7(1):113-6. PubMed ID: 5173356 [TBL] [Abstract][Full Text] [Related]
28. [Demyelination and leukodystrophy at an early age]. Seitelberger F Bol Estud Med Biol; 1981; 31(7-8):373-82. PubMed ID: 7347616 [No Abstract] [Full Text] [Related]
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30. Microglia damage precedes major myelin breakdown in X-linked adrenoleukodystrophy and metachromatic leukodystrophy. Bergner CG; van der Meer F; Winkler A; Wrzos C; Türkmen M; Valizada E; Fitzner D; Hametner S; Hartmann C; Pfeifenbring S; Stoltenburg-Didinger G; Brück W; Nessler S; Stadelmann C Glia; 2019 Jun; 67(6):1196-1209. PubMed ID: 30980503 [TBL] [Abstract][Full Text] [Related]
31. Enhancing cranial nerves and cauda equina: an emerging magnetic resonance imaging pattern in metachromatic leukodystrophy and krabbe disease. Morana G; Biancheri R; Dirocco M; Filocamo M; Marazzi MG; Pessagno A; Rossi A Neuropediatrics; 2009 Dec; 40(6):291-4. PubMed ID: 20446225 [TBL] [Abstract][Full Text] [Related]
32. The role of edema in diffuse sclerosis and other leukoencephalopathies. Feigin I; Budzilovich GN J Neuropathol Exp Neurol; 1978 May; 37(3):326-57. PubMed ID: 660219 [TBL] [Abstract][Full Text] [Related]
33. [Inborn errors of metabolism with preferred localization in the central nervous system]. Peiffer J Verh Dtsch Ges Pathol; 1982; 66():213-33. PubMed ID: 7184239 [No Abstract] [Full Text] [Related]
34. Myelin lesions associated with lysosomal and peroxisomal disorders. Faust PL; Kaye EM; Powers JM Expert Rev Neurother; 2010 Sep; 10(9):1449-66. PubMed ID: 20819015 [TBL] [Abstract][Full Text] [Related]
35. [Leukodystrophies: clinical aspects and findings with computerized tomography and magnetic resonance imaging]. Magnaldi S Radiol Med; 1991; 82(1-2):13-26. PubMed ID: 1896564 [TBL] [Abstract][Full Text] [Related]
36. Animal models of leukodystrophy: a new perspective for the development of therapies. Rutherford HA; Hamilton N FEBS J; 2019 Nov; 286(21):4176-4191. PubMed ID: 31520449 [TBL] [Abstract][Full Text] [Related]
37. The liver in lipid storage disease: biochemical basis of pathogenesis and clinical features. Brady RO; James SP; Barranger JA Prog Liver Dis; 1982; 7():331-46. PubMed ID: 6810410 [No Abstract] [Full Text] [Related]
38. Leukodystrophies with late disease onset: an update. Köhler W Curr Opin Neurol; 2010 Jun; 23(3):234-41. PubMed ID: 20216214 [TBL] [Abstract][Full Text] [Related]
39. Demyelinating hereditary neuropathies in children: a morphometric and ultrastructural study. Guzzetta F; Rodríguez J; Deodato M; Guzzetta A; Ferrière G Histol Histopathol; 1995 Jan; 10(1):91-104. PubMed ID: 7756749 [TBL] [Abstract][Full Text] [Related]