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Journal Abstract Search

137 related items for PubMed ID: 20091369

  • 1. Connatal Pelizaeus-Merzbacher disease: a great masquerader.
    Beri S, Hussain N, Gosalakkal JA.
    Indian J Pediatr; 2010 Mar; 77(3):338. PubMed ID: 20091369
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  • 5. Rare Case of Female with Pelizaeus Mertzbacher Disease due to deletion of Proteolipid Protein 1: A Case Report.
    Kinoshita M, Roston W.
    JNMA J Nepal Med Assoc; 2018 Mar; 56(214):967-969. PubMed ID: 31065145
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  • 7. A novel PLP1 mutation associated with optic nerve enlargement in two siblings with Pelizaeus-Merzbacher disease: A new MRI finding.
    Pavlidou E, Ramachandran V, Govender V, Wilson C, Das R, Vlachou V, Pavlou E, Saggar A, Mankad K, Kinali M.
    Brain Dev; 2017 Mar; 39(3):271-274. PubMed ID: 27793435
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  • 8. Connatal Pelizaeus-Merzbacher disease in two girls.
    Ziereisen F, Dan B, Christiaens F, Deltenre P, Boutemy R, Christophe C.
    Pediatr Radiol; 2000 Jul; 30(7):435-8. PubMed ID: 10929359
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  • 10. Pelizaeus-Merzbacher disease and spastic paraplegia type 2: two faces of myelin loss from mutations in the same gene.
    Hudson LD.
    J Child Neurol; 2003 Sep; 18(9):616-24. PubMed ID: 14572140
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  • 13. [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; 2003 Sep; 37(5):436-8. PubMed ID: 14533091
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  • 18. The spectrum of PLP1 gene mutations in patients with the classical form of the Pelizaeus-Merzbacher disease.
    Hoffman-Zacharska D, Mierzewska H, Szczepanik E, Poznański J, Mazurczak T, Jakubiuk-Tomaszuk A, Mądry J, Kierdaszuk A, Bal J.
    Med Wieku Rozwoj; 2013 Sep; 17(4):293-300. PubMed ID: 24519770
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  • 19. A novel proteolipid protein 1 gene mutation causing classical type Pelizaeus-Merzbacher disease.
    Fukumura S, Adachi N, Nagao M, Tsutsumi H.
    Brain Dev; 2011 Sep; 33(8):697-9. PubMed ID: 21177054
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