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Journal Abstract Search

111 related items for PubMed ID: 581221

  • 1. Congenital Pelizaeus-Merzbacher disease (Seitelberger type), malformation and cystic degeneration of the central nervous system.
    Vuia O.
    Neuropadiatrie; 1978 May; 9(2):172-84. PubMed ID: 581221
    [Abstract] [Full Text] [Related]

  • 2. Ultramicroscopic and histochemical studies of spongy degeneration (van Bogaert and Bertrand type).
    Adachi M, Wallace BJ, Volk BW.
    J Neuropathol Exp Neurol; 1967 Jan; 26(1):164-5. PubMed ID: 4290142
    [No Abstract] [Full Text] [Related]

  • 3. Absence of cerebral myelin sheaths in a case of presumed Pelizaeus-Merzbacher disease. Electron microscopic and biochemical studies.
    Watanabe I, McCaman R, Dyken P, Zeman W.
    J Neuropathol Exp Neurol; 1969 Apr; 28(2):243-56. PubMed ID: 5787430
    [No Abstract] [Full Text] [Related]

  • 4. Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher disease.
    Koeppen AH, Ronca NA, Greenfield EA, Hans MB.
    Ann Neurol; 1987 Feb; 21(2):159-70. PubMed ID: 3827224
    [Abstract] [Full Text] [Related]

  • 5. [van Bogaert-Bertrand spongy cerebral dystrophy].
    Strompen W, Diekmann L.
    Klin Padiatr; 1984 Feb; 196(2):111-4. PubMed ID: 6737947
    [Abstract] [Full Text] [Related]

  • 6. Fine structure of spongy degeneration of the central nervous system (van Bogaert and Bertrand type).
    Adachi M, Wallace BJ, Schneck L, Volk BW.
    J Neuropathol Exp Neurol; 1966 Oct; 25(4):598-616. PubMed ID: 4224221
    [No Abstract] [Full Text] [Related]

  • 7. Congenital spongy degeneration of the brain (van Bogaert - Bertrand) associated with micrencephaly and ponto - cerebellar atrophy (contributions to the pathology of glial dystrophy of intrauterin origin).
    Vuia O.
    Neuropadiatrie; 1977 Feb; 8(1):73-87. PubMed ID: 576735
    [Abstract] [Full Text] [Related]

  • 8. The neonatal progeroid syndrome (Wiedemann-Rautenstrauch) and its relationship to Pelizaeus-Merzbacher's disease.
    Ulrich J, Rudin C, Bubl R, Riederer BM.
    Neuropathol Appl Neurobiol; 1995 Apr; 21(2):116-20. PubMed ID: 7609841
    [Abstract] [Full Text] [Related]

  • 9. Protracted form of spongy degeneration of the central nervous system (van Bogaert and Bertrand type).
    Adachi M, Volk BW.
    Neurology; 1968 Nov; 18(11):1084-92. PubMed ID: 5751914
    [No Abstract] [Full Text] [Related]

  • 10. [Pathogenesis and pathomorphology of human leukodystrophies].
    Zhabotinskiĭ IuM, Shefer VF.
    Arkh Patol; 1981 Nov; 43(11):86-92. PubMed ID: 7032481
    [Abstract] [Full Text] [Related]

  • 11. Pelizacus-Merzbacher disease. Transitional form between classical and co-natal (Seitelberger) type.
    Jellinger K, Seitelberger F.
    Acta Neuropathol; 1969 Nov; 14(2):108-17. PubMed ID: 5347059
    [No Abstract] [Full Text] [Related]

  • 12. Magnetic resonance imaging in Pelizaeus-Merzbacher disease.
    Shimomura C, Matsui A, Choh H, Funahashi M, Suzuki Y, Tsuchiya K.
    Pediatr Neurol; 1988 Nov; 4(2):124-5. PubMed ID: 3242511
    [Abstract] [Full Text] [Related]

  • 13. Seitelberger's connatal form of Pelizaeus-Merzbacher Disease. Case report, clinical, pathological and biochemical findings.
    Ulrich J, Herschkowitz N.
    Acta Neuropathol; 1977 Oct 10; 40(2):129-36. PubMed ID: 201145
    [Abstract] [Full Text] [Related]

  • 14. The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Neuropathological study of a case.
    Martin JJ, Ceuterick CM, Leroy JG, Devos EA, Roelens JG.
    Neuropediatrics; 1984 Feb 10; 15(1):43-8. PubMed ID: 6200796
    [Abstract] [Full Text] [Related]

  • 15. [Pelizaeus-Merzbacher disease].
    Koetsveld-Baart JC, Glaudemans-van Gelderen IE, Valk J, Barth PG.
    Ned Tijdschr Geneeskd; 1993 Nov 27; 137(48):2494-8. PubMed ID: 8272126
    [Abstract] [Full Text] [Related]

  • 16. An MRI and MRS study of Pelizaeus-Merzbacher disease.
    Nezu A, Kimura S, Takeshita S, Osaka H, Kimura K, Inoue K.
    Pediatr Neurol; 1998 Apr 27; 18(4):334-7. PubMed ID: 9588530
    [Abstract] [Full Text] [Related]

  • 17. Structural manifestations of leukodystrophies.
    Seitelberger F.
    Neuropediatrics; 1984 Sep 27; 15 Suppl():53-61. PubMed ID: 6152813
    [Abstract] [Full Text] [Related]

  • 18. Overexpression of DM20 messenger RNA in two brothers with Pelizaeus-Merzbacher disease.
    Carango P, Funanage VL, Quirós RE, Debruyn CS, Marks HG.
    Ann Neurol; 1995 Oct 27; 38(4):610-7. PubMed ID: 7574457
    [Abstract] [Full Text] [Related]

  • 19. Tissue culture analysis of the inherited defect of central nervous system myelination in jimpy mice.
    Wolf MK, Holden AB.
    J Neuropathol Exp Neurol; 1969 Apr 27; 28(2):195-213. PubMed ID: 5787429
    [No Abstract] [Full Text] [Related]

  • 20. Pelizaeus-Merzbacher disease presenting as spinal muscular atrophy: clinical and molecular studies.
    Kaye EM, Doll RF, Natowicz MR, Smith FI.
    Ann Neurol; 1994 Dec 27; 36(6):916-9. PubMed ID: 7998780
    [Abstract] [Full Text] [Related]

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