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Journal Abstract Search

111 related items for PubMed ID: 9588530

  • 1. 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; 18(4):334-7. PubMed ID: 9588530
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  • 2. Magnetic resonance imaging in Pelizaeus-Merzbacher disease.
    Shimomura C, Matsui A, Choh H, Funahashi M, Suzuki Y, Tsuchiya K.
    Pediatr Neurol; 1988 Apr; 4(2):124-5. PubMed ID: 3242511
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  • 3. The magnetic resonance imaging spectrum of Pelizaeus-Merzbacher disease: A multicenter study of 19 patients.
    Sumida K, Inoue K, Takanashi J, Sasaki M, Watanabe K, Suzuki M, Kurahashi H, Omata T, Tanaka M, Yokochi K, Iio J, Iyoda K, Kurokawa T, Matsuo M, Sato T, Iwaki A, Osaka H, Kurosawa K, Yamamoto T, Matsumoto N, Maikusa N, Matsuda H, Sato N.
    Brain Dev; 2016 Jun; 38(6):571-80. PubMed ID: 26774704
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  • 4. Duplication of proteolipid protein gene: a possible major cause of Pelizaeus-Merzbacher disease.
    Wang PJ, Hwu WL, Lee WT, Wang TR, Shen YZ.
    Pediatr Neurol; 1997 Sep; 17(2):125-8. PubMed ID: 9367291
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  • 5. [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
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  • 6. Pelizaeus-Merzbacher-like disease: exclusion of the proteolipid protein locus and documentation of a new locus on Xq.
    Lazzarini A, Schwarz KO, Jiang S, Stenroos ES, Lehner T, Johnson WG.
    Neurology; 1997 Sep 27; 49(3):824-32. PubMed ID: 9305348
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  • 9. 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 27; 20(4):309-11. PubMed ID: 10328282
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  • 10. Congenital Pelizaeus-Merzbacher disease (Seitelberger type), malformation and cystic degeneration of the central nervous system.
    Vuia O.
    Neuropadiatrie; 1978 May 27; 9(2):172-84. PubMed ID: 581221
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  • 11. Two autopsy cases with Pelizaeus-Merzbacher disease phenotype of adult onset, without mutation of proteolipid protein gene.
    Sasaki A, Miyanaga K, Ototsuji M, Iwaki A, Iwaki T, Takahashi S, Nakazato Y.
    Acta Neuropathol; 2000 Jan 27; 99(1):7-13. PubMed ID: 10651021
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  • 13. A novel PLP1 frameshift mutation causing a milder form of Pelizaeus-Merzbacher disease.
    Shiihara T, Watanabe M, Moriyama K, Uematsu M, Sameshima K.
    Brain Dev; 2015 Apr 27; 37(4):455-8. PubMed ID: 25043250
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  • 15. A case of Pelizaeus-Merzbacher disease showing increased dosage of the proteolipid protein gene.
    Harding B, Ellis D, Malcolm S.
    Neuropathol Appl Neurobiol; 1995 Apr 27; 21(2):111-5. PubMed ID: 7541900
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  • 18. A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuria.
    Naidu S, Dlouhy SR, Geraghty MT, Hodes ME.
    J Inherit Metab Dis; 1997 Nov 27; 20(6):811-6. PubMed ID: 9427151
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  • 19. Girl with signs of Pelizaeus-Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene.
    Hodes ME, DeMyer WE, Pratt VM, Edwards MK, Dlouhy SR.
    Am J Med Genet; 1995 Feb 13; 55(4):397-401. PubMed ID: 7539211
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  • 20. Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher disease.
    Koeppen AH, Ronca NA, Greenfield EA, Hans MB.
    Ann Neurol; 1987 Feb 13; 21(2):159-70. PubMed ID: 3827224
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