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Journal Abstract Search

131 related items for PubMed ID: 5088756

  • 1. [Pelizaeus-Metzbacher disease: clinical diagnosis].
    Förster C, Daschner F, Murken JD.
    Z Kinderheilkd; 1971; 110(3):248-60. PubMed ID: 5088756
    [No Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. Autosomal recessive form of connatal Pelizaeus-Merzbacher disease.
    Begleiter ML, Harris DJ.
    Am J Med Genet; 1989 Jul 27; 33(3):311-3. PubMed ID: 2679088
    [Abstract] [Full Text] [Related]

  • 4. [Congenital Pelizaeus-Merzbacher disease simulating infantile spastic cerebral palsy].
    Carod Artal J, Prats Viñas JM, Garaizar Axpe C, Zuazo Zamalloa E.
    Neurologia; 1995 Jan 27; 10(1):57-8. PubMed ID: 7893516
    [No Abstract] [Full Text] [Related]

  • 5. [Infantile metachromatic leukodystrophy (4 cases)].
    Maraví E, Bueno M, Martínez-Lage JM, Villanueva JA.
    Arch Neurobiol (Madr); 1970 Jan 27; 33(2):207-32. PubMed ID: 4194760
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Progressive neurologic deterioration in a nine-year-old white male.
    Barness LA, Chandra S, Kling P, Laxova R, Allen DB, Gilbert-Barness E.
    Am J Med Genet; 1990 Dec 27; 37(4):489-503. PubMed ID: 2260594
    [No Abstract] [Full Text] [Related]

  • 8. [A case of Pelizaeus-Merzbacher disease with mainly mental symptomatology].
    Allegranza A, Alleva PM, Cescon I, Strada GP.
    Acta Neurol (Napoli); 1968 Dec 27; 23(6):895-911. PubMed ID: 5733445
    [No Abstract] [Full Text] [Related]

  • 9. Family with Pelizaeus-Merzbacher disease/X-linked spastic paraplegia and a nonsense mutation in exon 6 of the proteolipid protein gene.
    Bond C, Si X, Crisp M, Wong P, Paulson GW, Boesel CP, Dlouhy SR, Hodes ME.
    Am J Med Genet; 1997 Aug 22; 71(3):357-60. PubMed ID: 9268109
    [Abstract] [Full Text] [Related]

  • 10. [Clinical and genealogical report on a new family with three cases of adult metachromatic leukodystrophy].
    Wildbolz A.
    Schweiz Arch Neurol Neurochir Psychiatr; 1971 Aug 22; 109(2):313-21. PubMed ID: 5145365
    [No Abstract] [Full Text] [Related]

  • 11. [Sex-related neurologic diseases. Pelizaeus-Merzbacher-type leukodystrophy. Adrenoleukodystrophy. Fabry's disease].
    Pascual-Castroviejo I.
    An Esp Pediatr; 1984 Oct 22; 21 Suppl 20():44-7. PubMed ID: 6440461
    [No Abstract] [Full Text] [Related]

  • 12. [Chromosome study in a picture of probable leucodystrophy].
    Piazzesi W.
    Acta Neurol (Napoli); 1969 Oct 22; 24(2):319-27. PubMed ID: 5386350
    [No Abstract] [Full Text] [Related]

  • 13. [Two autopsy cases of diffuse cerebral sclerosis (Schilder's disease) in siblings].
    Kurokawa T, Takeshita K, Shirabe T, Mitsuyasu Y.
    Shinkei Kenkyu No Shimpo; 1969 Jun 22; 13(2):337-45. PubMed ID: 5390677
    [No Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. [Progressive syndrome of neurologic disorders in dizygotic twins].
    Gościńska Z, Bartoszewicz B.
    Neurol Neurochir Pol; 1969 Feb 13; 3(3):375-9. PubMed ID: 5803015
    [No Abstract] [Full Text] [Related]

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

  • 17. Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousins.
    Renier WO, Gabreëls FJ, Hustinx TW, Jaspar HH, Geelen JA, Van Haelst UJ, Lommen EJ, Ter Haar BG.
    Acta Neuropathol; 1981 Feb 13; 54(1):11-7. PubMed ID: 7234326
    [Abstract] [Full Text] [Related]

  • 18. Vestibular studies in Pelizaeus-Merzbacher disease.
    Mallinson AI, Longridge NS, Dunn HG, McCormick AQ.
    J Otolaryngol; 1983 Dec 13; 12(6):361-4. PubMed ID: 6663662
    [Abstract] [Full Text] [Related]

  • 19. [Contribution to the question of diffuse infantile cerebral sclerosis with primary dystrophy of the suprarenal gland].
    Riedel H.
    Psychiatr Neurol Med Psychol (Leipz); 1968 Feb 13; 20(2):67-73. PubMed ID: 5304006
    [No Abstract] [Full Text] [Related]

  • 20. Infantile globoid cell leucodystrophy (Krabbe's disease). A clinical and genetic study of 32 Swedish cases 1953--1967.
    Hagberg B, Kollberg H, Sourander P, Akesson HO.
    Neuropadiatrie; 1969 Feb 13; 1(1):74-88. PubMed ID: 5409293
    [No Abstract] [Full Text] [Related]

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