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Journal Abstract Search
137 related items for PubMed ID: 20091369
21. Pelizaeus-Merzbacher disease as a chromosomal disorder. Yamamoto T, Shimojima K. Congenit Anom (Kyoto); 2013 Mar; 53(1):3-8. PubMed ID: 23480352 [Abstract] [Full Text] [Related]
22. [Congenital cerebral hypomyelination---Pelizaeus-Merzbacher disease and associated disorders]. Inoue K, Iwaki A, Kurosawa K, Takanashi J, Deguchi K, Yamamoto T, Osaka H. No To Hattatsu; 2011 Nov; 43(6):435-42. PubMed ID: 22180957 [Abstract] [Full Text] [Related]
24. Pelizaeus-Merzbacher Disease due to PLP1 Frameshift Mutation in a Female with Nonrandom Skewed X-Chromosome Inactivation. Scala M, Traverso M, Capra V, Vari MS, Severino M, Grossi S, Zara F, Striano P, Minetti C. Neuropediatrics; 2019 Aug; 50(4):268-270. PubMed ID: 31137068 [No Abstract] [Full Text] [Related]
25. Characterization of a PLP-overexpressing transgenic rat, a model for the connatal form of Pelizaeus-Merzbacher disease. Mayer JA, Larsen EC, Kondo Y, Duncan ID. Neurobiol Dis; 2011 Nov; 44(2):231-8. PubMed ID: 21784154 [Abstract] [Full Text] [Related]
36. PLP1 gene duplication as a cause of the classic form of Pelizaeus-Merzbacher disease - case report. Mądry J, Hoffman-Zacharska D, Królicki L, Jakuciński M, Friedman A. Neurol Neurochir Pol; 2010 Feb 15; 44(5):511-5. PubMed ID: 21082496 [Abstract] [Full Text] [Related]