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Journal Abstract Search

397 related items for PubMed ID: 18851904

  • 1. Diffuse cerebral hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum.
    Sasaki M, Takanashi J, Tada H, Sakuma H, Furushima W, Sato N.
    Brain Dev; 2009 Sep; 31(8):582-7. PubMed ID: 18851904
    [Abstract] [Full Text] [Related]

  • 2. Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.
    van der Knaap MS, Linnankivi T, Paetau A, Feigenbaum A, Wakusawa K, Haginoya K, Köhler W, Henneke M, Dinopoulos A, Grattan-Smith P, Brockmann K, Schiffmann R, Blaser S.
    Neurology; 2007 Jul 10; 69(2):166-71. PubMed ID: 17620549
    [Abstract] [Full Text] [Related]

  • 3. Childhood ataxia with cerebral hypomyelination (CACH) syndrome: a study of three siblings.
    Vaidya SR, Desai SB, Khadilkar SV, Mehta NA.
    Neurol India; 2004 Sep 10; 52(3):372-4. PubMed ID: 15472431
    [Abstract] [Full Text] [Related]

  • 4. A case with central and peripheral hypomyelination with hypogonadotropic hypogonadism and hypodontia (4H syndrome) plus cataract.
    Sato I, Onuma A, Goto N, Sakai F, Fujiwara I, Uematsu M, Osaka H, Okahashi S, Nonaka I, Tanaka S, Haginoya K.
    J Neurol Sci; 2011 Jan 15; 300(1-2):179-81. PubMed ID: 20884016
    [Abstract] [Full Text] [Related]

  • 5. Diffuse central hypomyelination presenting as 4H syndrome caused by compound heterozygous mutations in POLR3A encoding the catalytic subunit of polymerase III.
    Terao Y, Saitsu H, Segawa M, Kondo Y, Sakamoto K, Matsumoto N, Tsuji S, Nomura Y.
    J Neurol Sci; 2012 Sep 15; 320(1-2):102-5. PubMed ID: 22819058
    [Abstract] [Full Text] [Related]

  • 6. Leukoencephalopathy with ataxia, hypodontia, and hypomyelination.
    Wolf NI, Harting I, Boltshauser E, Wiegand G, Koch MJ, Schmitt-Mechelke T, Martin E, Zschocke J, Uhlenberg B, Hoffmann GF, Weber L, Ebinger F, Rating D.
    Neurology; 2005 Apr 26; 64(8):1461-4. PubMed ID: 15851747
    [Abstract] [Full Text] [Related]

  • 7. Natural history of adult-onset eIF2B-related disorders: a multi-centric survey of 16 cases.
    Labauge P, Horzinski L, Ayrignac X, Blanc P, Vukusic S, Rodriguez D, Mauguiere F, Peter L, Goizet C, Bouhour F, Denier C, Confavreux C, Obadia M, Blanc F, de Sèze J, Fogli A, Boespflug-Tanguy O.
    Brain; 2009 Aug 26; 132(Pt 8):2161-9. PubMed ID: 19625339
    [Abstract] [Full Text] [Related]

  • 8. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.
    Pascual-Castroviejo I, Gutierrez M, Morales C, Gonzalez-Mediero I, Martínez-Bermejo A, Pascual-Pascual SI.
    Neuropediatrics; 1994 Aug 26; 25(4):183-90. PubMed ID: 7824090
    [Abstract] [Full Text] [Related]

  • 9. Hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC). Report of a new case.
    Mercimek-Mahmutoglu S, van der Knaap MS, Baric I, Prayer D, Stoeckler-Ipsiroglu S.
    Neuropediatrics; 2005 Jun 26; 36(3):223-6. PubMed ID: 15944912
    [Abstract] [Full Text] [Related]

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  • 11. Extent of cerebellum, subcortical and cortical atrophy in patients with MS: a case-control study.
    Ramasamy DP, Benedict RH, Cox JL, Fritz D, Abdelrahman N, Hussein S, Minagar A, Dwyer MG, Zivadinov R.
    J Neurol Sci; 2009 Jul 15; 282(1-2):47-54. PubMed ID: 19201003
    [Abstract] [Full Text] [Related]

  • 12. [Central hypomyelination, hypogonadotrophic hypogonadism and hypodontia: a new leukodystrophy].
    Vázquez-López M, Ruiz-Martín Y, de Castro-Castro P, Garzo-Fernández C, Martín-del Valle F, Márquez-de la Plata L.
    Rev Neurol; 2009 Jul 15; 47(4):204-8. PubMed ID: 18671210
    [Abstract] [Full Text] [Related]

  • 13. An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia.
    Aykut A, Cogulu O, Ekmekci AY, Ozkinay F.
    Genet Couns; 2008 Jul 15; 19(2):237-40. PubMed ID: 18618999
    [Abstract] [Full Text] [Related]

  • 14. Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matter.
    Tohyama J, Akasaka N, Osaka H, Maegaki Y, Kato M, Saito N, Yamashita S, Ohno K.
    Brain Dev; 2008 May 15; 30(5):349-55. PubMed ID: 18065176
    [Abstract] [Full Text] [Related]

  • 15. Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset.
    Brockmann K, Simpson MA, Faber A, Bönnemann C, Crosby AH, Gärtner J.
    Neuropediatrics; 2005 Aug 15; 36(4):274-8. PubMed ID: 16138254
    [Abstract] [Full Text] [Related]

  • 16. [Familial cases of spastic paraparesis, mental disturbance and thinning of the corpus callosum].
    Honda Y, Sugihara E, Hino H, Shoji H, Oizumi K.
    Rinsho Shinkeigaku; 1993 May 15; 33(5):507-13. PubMed ID: 8365056
    [Abstract] [Full Text] [Related]

  • 17. [Cerebellar ataxia of Norman-Jaeken. Presentation of seven Spanish patients].
    Pascual-Castroviejo I, Pascual-Pascual SI, Quijano-Roy S, Gutiérrez-Molina M, Morales MC, Velázquez-Fragua R, Maties M.
    Rev Neurol; 1993 May 15; 42(12):723-8. PubMed ID: 16775797
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  • 20. [A case of spastic paraparesis, mental retardation and thinning of corpus callosum].
    Sugama S, Kusano K, Nemoto K.
    Rinsho Shinkeigaku; 1995 Feb 15; 35(2):215-7. PubMed ID: 7781244
    [Abstract] [Full Text] [Related]

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