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Journal Abstract Search

112 related items for PubMed ID: 7609841

  • 1. 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]

  • 2. 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; 15(1):43-8. PubMed ID: 6200796
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Pelizaeus-Merzbacher disease.
    Stark G.
    Dev Med Child Neurol; 1972 Dec; 14(6):806-9. PubMed ID: 4643440
    [No Abstract] [Full Text] [Related]

  • 5. [Anatomo-clinical and neurochemical aspects of Pelizaeus-Merzbacher disease].
    Leclercq JP, Andersson JC, Davy JP, Lorteau P, Poilpre E.
    Encephale; 1982 Dec; 8(3):377-88. PubMed ID: 7186459
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. The reflection of histology in MR imaging of Pelizaeus-Merzbacher disease.
    van der Knaap MS, Valk J.
    AJNR Am J Neuroradiol; 1989 Apr; 10(1):99-103. PubMed ID: 2492735
    [Abstract] [Full Text] [Related]

  • 9. Pelizaeus-Merzbacher disease: biochemical analysis of isolated myelin (electron-microscopy; protein, lipid and unsubstituted fatty acids analysis).
    Bourre JM, Jacque C, Nguyen-Legros J, Bornhofen JH, Araoz CA, Daudu O, Baumann NA.
    Eur Neurol; 1978 Apr; 17(6):317-26. PubMed ID: 744198
    [Abstract] [Full Text] [Related]

  • 10. An autopsy case of classical Pelizaeus-Merzbacher's disease.
    Konishi Y, Kamoshita S.
    Acta Neuropathol; 1975 Apr; 31(3):267-70. PubMed ID: 1138535
    [Abstract] [Full Text] [Related]

  • 11. Jimpy, an anomaly of, myelin maturation. Biochemical study of myelination phases.
    Matthieu JM, Widmer S, Herschkowitz.
    Brain Res; 1973 Jun 15; 55(2):403-12. PubMed ID: 4123465
    [No Abstract] [Full Text] [Related]

  • 12. Connatal Pelizaeus-Merzbacher disease associated with the jimpy(msd) mice mutation.
    Komaki H, Sasaki M, Yamamoto T, Iai M, Takashima S.
    Pediatr Neurol; 1999 Apr 15; 20(4):309-11. PubMed ID: 10328282
    [Abstract] [Full Text] [Related]

  • 13. A sporadic case of presumed Pelizaeus-Merzbacher disease.
    Liaño H, Ricoy JR, Díaz-Flores L, Gimeno A.
    Eur Neurol; 1974 Apr 15; 11(5):304-16. PubMed ID: 4850312
    [No Abstract] [Full Text] [Related]

  • 14. [Oligophrenia--selected syndrome LIII. Pelizaeus-Merzbacher's syndrome].
    Hansen E.
    Ugeskr Laeger; 1976 May 24; 138(22):1329-30. PubMed ID: 1273950
    [No Abstract] [Full Text] [Related]

  • 15. Peculiar dysmorphic syndrome with orthochromatic leucodystrophy. Discussion of its relationship with Cockayne's syndrome and Pelizaeus-Merzbacher's disease.
    Martin JJ, Deberdt R, Philippart M, Van Acker KJ, Hooft C.
    Acta Neuropathol; 1971 May 24; 18(3):224-33. PubMed ID: 5561979
    [No Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Early lesion of Pelizaeus-Merzbacher disease: electron microscopic and biochemical study.
    Watanabe I, Patel V, Goebel HH, Siakotos AN, Zeman W, DeMyer W, Dyer JS.
    J Neuropathol Exp Neurol; 1973 Apr 10; 32(2):313-33. PubMed ID: 4123133
    [No Abstract] [Full Text] [Related]

  • 18. Sudanophilic leucodystrophy: report of a case with tigroid demyelination of the centrum ovale.
    Rizzuto N, Pennelli N, Giordano R.
    Acta Neuropathol; 1976 Mar 30; 34(3):267-71. PubMed ID: 1266582
    [Abstract] [Full Text] [Related]

  • 19. Structural manifestations of leukodystrophies.
    Seitelberger F.
    Neuropediatrics; 1984 Sep 30; 15 Suppl():53-61. PubMed ID: 6152813
    [Abstract] [Full Text] [Related]

  • 20. Cerebral lipid composition during myelination in murine genetic leukodystrophies.
    Hogan EL, Joseph KC.
    Neurology; 1970 Apr 30; 20(4):416. PubMed ID: 5535077
    [No Abstract] [Full Text] [Related]

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