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Journal Abstract Search

740 related items for PubMed ID: 17620549

  • 1. 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]

  • 2. 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]

  • 3. 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]

  • 4. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.
    Le Ber I, Clot F, Vercueil L, Camuzat A, Viémont M, Benamar N, De Liège P, Ouvrard-Hernandez AM, Pollak P, Stevanin G, Brice A, Dürr A.
    Neurology; 2006 Nov 28; 67(10):1769-73. PubMed ID: 17130408
    [Abstract] [Full Text] [Related]

  • 5. 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 28; 31(8):582-7. PubMed ID: 18851904
    [Abstract] [Full Text] [Related]

  • 6. Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation.
    Hamilton EM, Polder E, Vanderver A, Naidu S, Schiffmann R, Fisher K, Raguž AB, Blumkin L, H-ABC Research Group, van Berkel CG, Waisfisz Q, Simons C, Taft RJ, Abbink TE, Wolf NI, van der Knaap MS.
    Brain; 2014 Jul 28; 137(Pt 7):1921-30. PubMed ID: 24785942
    [Abstract] [Full Text] [Related]

  • 7. Distinctive MRI findings in pallidopontonigral degeneration (PPND).
    Frank AR, Wszolek ZK, Jack CR, Boeve BF.
    Neurology; 2007 Feb 20; 68(8):620-1. PubMed ID: 17310038
    [No Abstract] [Full Text] [Related]

  • 8. Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17).
    Lasek K, Lencer R, Gaser C, Hagenah J, Walter U, Wolters A, Kock N, Steinlechner S, Nagel M, Zühlke C, Nitschke MF, Brockmann K, Klein C, Rolfs A, Binkofski F.
    Brain; 2006 Sep 20; 129(Pt 9):2341-52. PubMed ID: 16760196
    [Abstract] [Full Text] [Related]

  • 9. Different patterns of cerebellar abnormality and hypomyelination between POLR3A and POLR3B mutations.
    Takanashi J, Osaka H, Saitsu H, Sasaki M, Mori H, Shibayama H, Tanaka M, Nomura Y, Terao Y, Inoue K, Matsumoto N, Barkovich AJ.
    Brain Dev; 2014 Mar 20; 36(3):259-63. PubMed ID: 23643445
    [Abstract] [Full Text] [Related]

  • 10. [Hypomyelination with atrophy of the basal ganglia and cerebellum. Contribution of two new cases to a recently reported entity].
    Tomás-Vila M, Menor F, Ley-Martos M, Jumillas-Luján MJ, Marco-Hernández AV, Barbero P.
    Rev Neurol; 2014 Feb 16; 58(4):161-5. PubMed ID: 24504878
    [Abstract] [Full Text] [Related]

  • 11. New subform of the late infantile form of neuronal ceroid lipofuscinosis.
    Wisniewski KE, Kida E, Connell F, Elleder M, Eviatar L, Konkol RJ.
    Neuropediatrics; 1993 Jun 16; 24(3):155-63. PubMed ID: 8355821
    [Abstract] [Full Text] [Related]

  • 12. Patterns of fractional anisotropy changes in white matter of cerebellar peduncles distinguish spinocerebellar ataxia-1 from multiple system atrophy and other ataxia syndromes.
    Prakash N, Hageman N, Hua X, Toga AW, Perlman SL, Salamon N.
    Neuroimage; 2009 Aug 16; 47 Suppl 2():T72-81. PubMed ID: 19446636
    [Abstract] [Full Text] [Related]

  • 13. Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I.
    Harting I, Neumaier-Probst E, Seitz A, Maier EM, Assmann B, Baric I, Troncoso M, Mühlhausen C, Zschocke J, Boy NP, Hoffmann GF, Garbade SF, Kölker S.
    Brain; 2009 Jul 16; 132(Pt 7):1764-82. PubMed ID: 19433437
    [Abstract] [Full Text] [Related]

  • 14. Voxel-based morphometry and voxel-based relaxometry in multiple system atrophy-a comparison between clinical subtypes and correlations with clinical parameters.
    Minnerop M, Specht K, Ruhlmann J, Schimke N, Abele M, Weyer A, Wüllner U, Klockgether T.
    Neuroimage; 2007 Jul 15; 36(4):1086-95. PubMed ID: 17512219
    [Abstract] [Full Text] [Related]

  • 15. MRI lesion profiles in sporadic Creutzfeldt-Jakob disease.
    Meissner B, Kallenberg K, Sanchez-Juan P, Collie D, Summers DM, Almonti S, Collins SJ, Smith P, Cras P, Jansen GH, Brandel JP, Coulthart MB, Roberts H, Van Everbroeck B, Galanaud D, Mellina V, Will RG, Zerr I.
    Neurology; 2009 Jun 09; 72(23):1994-2001. PubMed ID: 19506221
    [Abstract] [Full Text] [Related]

  • 16. 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 09; 132(Pt 8):2161-9. PubMed ID: 19625339
    [Abstract] [Full Text] [Related]

  • 17. 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 09; 25(4):183-90. PubMed ID: 7824090
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Differential diagnosis of cerebellar atrophy in childhood.
    Poretti A, Wolf NI, Boltshauser E.
    Eur J Paediatr Neurol; 2008 May 15; 12(3):155-67. PubMed ID: 17869142
    [Abstract] [Full Text] [Related]

  • 20. [Autosomal recessive hereditary cortical cerebellar atrophy with striatal degeneration--two siblings showing choreoathetoid movement, ataxia, dementia, and amenorrhea].
    Iwabuchi K, Nakazawa Y, Akai J, Yagishita S, Amano N.
    No To Shinkei; 1994 Jun 15; 46(6):563-71. PubMed ID: 8068439
    [Abstract] [Full Text] [Related]

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