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Journal Abstract Search

111 related items for PubMed ID: 581221

  • 21. [Tardive spino-cerebellar degeneration with amyotrophia, complicating a severe case of pallido-luysian degeneration and diffuse histological lesions of senility. (Anatomo-clinical study of a case with nosographic discussion)].
    Boudouresques J, Toga M, Khalil R, Chérif AA, Pellissier JF, Gosset A.
    Rev Neurol (Paris); 1976 Sep; 132(9):623-37. PubMed ID: 996389
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  • 22. Schwann cell remyelination of demyelinated axons in spinal cord multiple sclerosis lesions.
    Itoyama Y, Webster HD, Richardson EP, Trapp BD.
    Ann Neurol; 1983 Sep; 14(3):339-46. PubMed ID: 6195956
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  • 25. [Anatomo-clinical and neurochemical aspects of Pelizaeus-Merzbacher disease].
    Leclercq JP, Andersson JC, Davy JP, Lorteau P, Poilpre E.
    Encephale; 1982 Sep; 8(3):377-88. PubMed ID: 7186459
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  • 26. The reflection of histology in MR imaging of Pelizaeus-Merzbacher disease.
    van der Knaap MS, Valk J.
    AJNR Am J Neuroradiol; 1989 Sep; 10(1):99-103. PubMed ID: 2492735
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  • 28. Myelin mosaicism and brain plasticity in heterozygous females of a canine X-linked trait.
    Cuddon PA, Lipsitz D, Duncan ID.
    Ann Neurol; 1998 Nov; 44(5):771-9. PubMed ID: 9818933
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  • 29. Myelination of a fetus with Pelizaeus-Merzbacher disease: immunopathological study.
    Shiraishi K, Itoh M, Sano K, Takashima S, Kubota T.
    Ann Neurol; 2003 Aug; 54(2):259-62. PubMed ID: 12891682
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  • 30. The fine structure of the cerebella of a model of an inherited leukodystrophy in jimpy mice and their "normal" litter mates.
    Hirano A, Sax DS, Zimmerman HM.
    Trans Am Neurol Assoc; 1969 Aug; 94():174-7. PubMed ID: 5374432
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  • 32. [Leukodystrophy with strio-cerebellar calcification, microcephaly and dwarfism].
    Lyon G, Robain O, Philippart M, Sarliève L.
    Rev Neurol (Paris); 1968 Aug; 119(2):197-210. PubMed ID: 5702873
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  • 33. Familial spongy degeneration of the central nervous system (Van Bogaert-Bertrand disease). An ultrastructural study.
    Gambetti P, Mellman WJ, Gonatas NK.
    Acta Neuropathol; 1969 Jan 31; 12(2):103-15. PubMed ID: 5789730
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  • 35. Pelizaeus-Merzbacher disease: pathogenic mechanisms and insights into the roles of proteolipid protein 1 in the nervous system.
    Garbern JY.
    J Neurol Sci; 2005 Feb 15; 228(2):201-3. PubMed ID: 15694206
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  • 37. Histochemical, ultrastructural and biochemical studies of a case with leukodystrophy due to congenital deficiency of myelin.
    Adachi M, Schneck L, Torii J, Volk BW.
    J Neuropathol Exp Neurol; 1970 Oct 15; 29(4):601-14. PubMed ID: 5471924
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  • 38. The twitcher mouse. Central nervous system pathology after bone marrow transplantation.
    Suzuki K, Hoogerbrugge PM, Poorthuis BJ, Bekkum DW, Suzuki K.
    Lab Invest; 1988 Mar 15; 58(3):302-9. PubMed ID: 3279262
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  • 39. Ultrastructure of central nervous system lesions in metachromatic leukodystrophy with special reference to morphogenesis.
    Liu HM.
    J Neuropathol Exp Neurol; 1968 Oct 15; 27(4):624-44. PubMed ID: 5303218
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  • 40. Jimpy(msd) mouse mutation and connatal Pelizaeus-Merzbacher disease.
    Yamamoto T, Nanba E, Zhang H, Sasaki M, Komaki H, Takeshita K.
    Am J Med Genet; 1998 Feb 03; 75(4):439-40. PubMed ID: 9482656
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