These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

94 related items for PubMed ID: 26279330

  • 1. Callosal disconnection syndrome in symptomatic female carrier of Pelizaeus-Merzbacher disease.
    Kim Y, Asano Y, Koide R, Kimura H, Saitsu H, Matsumoto N, Bandoh M.
    J Neurol Sci; 2015 Nov 15; 358(1-2):461-2. PubMed ID: 26279330
    [No Abstract] [Full Text] [Related]

  • 2. Callosal disconnection and limb-kinetic apraxia.
    Acosta LM, Bennett JA, Heilman KM.
    Neurocase; 2014 Nov 15; 20(6):599-605. PubMed ID: 23972140
    [Abstract] [Full Text] [Related]

  • 3. Teaching video neuroimages: callosal apraxia: a straightforward model of ideomotor apraxia.
    Jablonski K, Antoniello D.
    Neurology; 2013 May 28; 80(22):e239. PubMed ID: 23713093
    [Abstract] [Full Text] [Related]

  • 4. Callosal ideomotor apraxia in Alzheimer's disease.
    Cimino-Knight AM, Gonzalez Rothi LJ, He Y, Heilman KM.
    J Clin Exp Neuropsychol; 2017 Feb 28; 39(1):1-8. PubMed ID: 27829324
    [Abstract] [Full Text] [Related]

  • 5. Improvement in callosal disconnection syndrome with recovery of callosal connectivity.
    Morihara K, Kakinuma K, Kobayashi E, Kawakami N, Narita W, Kanno S, Tanaka F, Suzuki K.
    Neurocase; 2021 Jun 28; 27(3):323-331. PubMed ID: 34365896
    [Abstract] [Full Text] [Related]

  • 6. Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects.
    Vaurs-Barrière C, Deville M, Sarret C, Giraud G, Des Portes V, Prats-Viñas JM, De Michele G, Dan B, Brady AF, Boespflug-Tanguy O, Touraine R.
    Ann Neurol; 2009 Jan 28; 65(1):114-8. PubMed ID: 19194886
    [Abstract] [Full Text] [Related]

  • 7. Three new PLP1 splicing mutations demonstrate pathogenic and phenotypic diversity of Pelizaeus-Merzbacher disease.
    Laššuthová P, Žaliová M, Inoue K, Haberlová J, Sixtová K, Sakmaryová I, Paděrová K, Mazanec R, Zámečník J, Šišková D, Garbern J, Seeman P.
    J Child Neurol; 2014 Jul 28; 29(7):924-31. PubMed ID: 23771846
    [Abstract] [Full Text] [Related]

  • 8. Diffusion tensor imaging of patients with proteolipid protein 1 gene mutations.
    Laukka JJ, Makki MI, Lafleur T, Stanley J, Kamholz J, Garbern JY.
    J Neurosci Res; 2014 Dec 28; 92(12):1723-32. PubMed ID: 25156430
    [Abstract] [Full Text] [Related]

  • 9. A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection of PLP1 gene duplication in Pelizaeus-Merzbacher disease.
    Hobson G, Stabley D, Funanage V, Marks H.
    Hum Mutat; 2001 Feb 28; 17(2):152. PubMed ID: 11180600
    [Abstract] [Full Text] [Related]

  • 10. Callosal apraxia: a 34-year follow-up study.
    Falchook AD, Watson RT, Heilman KM.
    Neurocase; 2016 Jun 28; 22(3):306-11. PubMed ID: 26928117
    [Abstract] [Full Text] [Related]

  • 11. 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 28; 37(4):455-8. PubMed ID: 25043250
    [Abstract] [Full Text] [Related]

  • 12. Variable expression of a novel PLP1 mutation in members of a family with Pelizaeus-Merzbacher disease.
    Fattal-Valevski A, DiMaio MS, Hisama FM, Hobson GM, Davis-Williams A, Garbern JY, Mahoney MJ, Kolodny EH, Pastores GM.
    J Child Neurol; 2009 May 28; 24(5):618-24. PubMed ID: 19151366
    [Abstract] [Full Text] [Related]

  • 13. Disrupted SOX10 regulation of GJC2 transcription causes Pelizaeus-Merzbacher-like disease.
    Osaka H, Hamanoue H, Yamamoto R, Nezu A, Sasaki M, Saitsu H, Kurosawa K, Shimbo H, Matsumoto N, Inoue K.
    Ann Neurol; 2010 Aug 28; 68(2):250-4. PubMed ID: 20695017
    [Abstract] [Full Text] [Related]

  • 14. [Pelizaeus-Merzbacher disease(PMD)/spastic paraplegia 2(SPG2)].
    Eto Y.
    Ryoikibetsu Shokogun Shirizu; 2000 Aug 28; (29 Pt 4):536-7. PubMed ID: 11032015
    [No Abstract] [Full Text] [Related]

  • 15. Cognitive-motor dysfunction after severe traumatic brain injury: A cerebral interhemispheric disconnection syndrome.
    Falchook AD, Porges EC, Nadeau SE, Leon SA, Williamson JB, Heilman KM.
    J Clin Exp Neuropsychol; 2015 Aug 28; 37(10):1062-73. PubMed ID: 26340588
    [Abstract] [Full Text] [Related]

  • 16. [Interhemispheric disconnection syndrome caused by partial infarction of the corpus callosum: neuropsychological study and MRI].
    Servan J, Verstichel P, Elghozi D, Duclos H.
    Rev Neurol (Paris); 1996 Mar 28; 152(3):165-73. PubMed ID: 8761626
    [Abstract] [Full Text] [Related]

  • 17. Pelizaeus-Merzbacher disease: pathogenic mechanisms and insights into the roles of proteolipid protein 1 in the nervous system.
    Garbern JY.
    J Neurol Sci; 2005 Feb 15; 228(2):201-3. PubMed ID: 15694206
    [No Abstract] [Full Text] [Related]

  • 18. Magnetic resonance imaging traits may help to differentiate Pelizaeus-Merzbacher and Pelizaeus-Merzbacher-like disease.
    Castro MAA, Fraiman PHA, Godeiro-Junior CO.
    Arq Neuropsiquiatr; 2019 Sep 05; 77(8):594. PubMed ID: 31508687
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. [Duplication of the PLP gene and the classical form of Pelizaeus-Merzbacher disease].
    Blanco-Barca MO, Eirís-Puñal J, Soler-Regal C, Castro-Gago M.
    Rev Neurol; 2019 Sep 05; 37(5):436-8. PubMed ID: 14533091
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.