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PUBMED FOR HANDHELDS

Journal Abstract Search

137 related items for PubMed ID: 16802726

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  • 22. 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; 17(4):293-300. PubMed ID: 24519770
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  • 24. A brief history of Pelizaeus-Merzbacher disease and proteolipid protein.
    Koeppen AH.
    J Neurol Sci; 2005 Feb 15; 228(2):198-200. PubMed ID: 15694205
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  • 29. Connatal Pelizaeus-Merzbacher disease: a great masquerader.
    Beri S, Hussain N, Gosalakkal JA.
    Indian J Pediatr; 2010 Mar 15; 77(3):338. PubMed ID: 20091369
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  • 35. 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 15; 17(2):152. PubMed ID: 11180600
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  • 36. Mild phenotype in Pelizaeus-Merzbacher disease caused by a PLP1-specific mutation.
    Osaka H, Koizume S, Aoyama H, Iwamoto H, Kimura S, Nagai J, Kurosawa K, Yamashita S.
    Brain Dev; 2010 Oct 15; 32(9):703-7. PubMed ID: 20022439
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  • 39. A splicing mutation of proteolipid protein 1 in Pelizaeus-Merzbacher disease.
    Omata T, Nagai J, Shimbo H, Koizume S, Miyagi Y, Kurosawa K, Yamashita S, Osaka H, Inoue K.
    Brain Dev; 2016 Jun 15; 38(6):581-4. PubMed ID: 26725305
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  • 40. 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 15; 33(8):697-9. PubMed ID: 21177054
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