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

155 related items for PubMed ID: 39322379

  • 1. Inherited white matter disorders: Hypomyelination (myelin disorders).
    Perrier S, Gauquelin L, Bernard G.
    Handb Clin Neurol; 2024; 204():197-223. PubMed ID: 39322379
    [Abstract] [Full Text] [Related]

  • 2. Neurogenetics of Pelizaeus-Merzbacher disease.
    Osório MJ, Goldman SA.
    Handb Clin Neurol; 2018; 148():701-722. PubMed ID: 29478609
    [Abstract] [Full Text] [Related]

  • 3. Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder.
    Lossos A, Elazar N, Lerer I, Schueler-Furman O, Fellig Y, Glick B, Zimmerman BE, Azulay H, Dotan S, Goldberg S, Gomori JM, Ponger P, Newman JP, Marreed H, Steck AJ, Schaeren-Wiemers N, Mor N, Harel M, Geiger T, Eshed-Eisenbach Y, Meiner V, Peles E.
    Brain; 2015 Sep; 138(Pt 9):2521-36. PubMed ID: 26179919
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Novel pathologic findings in patients with Pelizaeus-Merzbacher disease.
    Laukka JJ, Kamholz J, Bessert D, Skoff RP.
    Neurosci Lett; 2016 Aug 03; 627():222-32. PubMed ID: 27222925
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. 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
    [Abstract] [Full Text] [Related]

  • 18. Oligodendroglial transcription factor (OLIG1 and OLIG2) mutations are not associated with Pelizaeus-Merzbacher-like leukodystrophy.
    Ruf N, Martelli M, Weschke B, Uhlenberg B.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Apr 05; 144B(3):365-6. PubMed ID: 17171653
    [Abstract] [Full Text] [Related]

  • 19. GJC2 promoter mutations causing Pelizaeus-Merzbacher-like disease.
    Gotoh L, Inoue K, Helman G, Mora S, Maski K, Soul JS, Bloom M, Evans SH, Goto YI, Caldovic L, Hobson GM, Vanderver A.
    Mol Genet Metab; 2014 Mar 05; 111(3):393-398. PubMed ID: 24374284
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.