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Journal Abstract Search

88 related items for PubMed ID: 19922087

  • 1. Pelizaeus Merzbacher disease: morphological analysis of the vestibulo-cochlear system.
    Schmutzhard J, Schwentner I, Glueckert R, Sergi C, Beckmann F, Abraham I, Riechelmann H, Schrott-Fischer A, Müller B.
    Acta Otolaryngol; 2009 Dec; 129(12):1395-9. PubMed ID: 19922087
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  • 2. Clinical neurophysiology in GJA12-related hypomyelination vs Pelizaeus-Merzbacher disease.
    Henneke M, Gegner S, Hahn A, Plecko-Startinig B, Weschke B, Gärtner J, Brockmann K.
    Neurology; 2010 Jun 01; 74(22):1785-9. PubMed ID: 20513814
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  • 3. [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; 2010 Jun 01; 37(5):436-8. PubMed ID: 14533091
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  • 5. 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
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  • 7. Pelizaeus-Merzbacher disease, easily misdiagnosed as cerebral palsy: a report of a three-generation family.
    Chen YC, Liang WC, Su YN, Jong YJ.
    Pediatr Neonatol; 2014 Apr 05; 55(2):150-3. PubMed ID: 23597542
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  • 10. Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications.
    Shimojima K, Inoue T, Hoshino A, Kakiuchi S, Watanabe Y, Sasaki M, Nishimura A, Takeshita-Yanagisawa A, Tajima G, Ozawa H, Kubota M, Tohyama J, Sasaki M, Oka A, Saito K, Osawa M, Yamamoto T.
    Brain Dev; 2010 Mar 05; 32(3):171-9. PubMed ID: 19328639
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  • 12. Myelination of a fetus with Pelizaeus-Merzbacher disease: immunopathological study.
    Shiraishi K, Itoh M, Sano K, Takashima S, Kubota T.
    Ann Neurol; 2003 Aug 05; 54(2):259-62. PubMed ID: 12891682
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  • 13. 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 05; 17(2):152. PubMed ID: 11180600
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  • 14. 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 05; 92(12):1723-32. PubMed ID: 25156430
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  • 18. Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.
    Kuan CC, Sano M, Kaga K, Kodama M, Kodama K.
    Acta Otolaryngol; 2008 May 05; 128(5):539-46. PubMed ID: 18421608
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  • 19. The molecular and cellular defects underlying Pelizaeus-Merzbacher disease.
    Woodward KJ.
    Expert Rev Mol Med; 2008 May 19; 10():e14. PubMed ID: 18485258
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  • 20. Insertion of an extra copy of Xq22.2 into 1p36 results in functional duplication of the PLP1 gene in a girl with classical Pelizaeus-Merzbacher disease.
    Masliah-Planchon J, Dupont C, Vartzelis G, Trimouille A, Eymard-Pierre E, Gay-Bellile M, Renaldo F, Dorboz I, Pagan C, Quentin S, Elmaleh M, Kotsogianni C, Konstantelou E, Drunat S, Tabet AC, Boespflug-Tanguy O.
    BMC Med Genet; 2015 Sep 02; 16():77. PubMed ID: 26329556
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