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28. 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]
29. 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 [Abstract] [Full Text] [Related]
31. [A case of callosal damage accompanied with ideomotor apraxia without agraphia, diagnostic apraxia and intermittent initiation difficulty of left hand]. Toshiya F, Endou K, Sugishita M, Tsukakoshi H. Rinsho Shinkeigaku; 1987 Aug; 27(8):1073-80. PubMed ID: 3690922 [No Abstract] [Full Text] [Related]
32. [Pelizaeus-Merzbacher-caused diseases in Connexin 46 mutation: a rare form of leukodystrophy]. Fritz GA, Simbrunner J, Deutschmann HA. Rofo; 2007 Jun; 179(6):637-8. PubMed ID: 17492548 [No Abstract] [Full Text] [Related]
37. Pelizaeus-Merzbacher disease: electrophysiological study of two sibs with the classic form and of their relatives. Alfonsi E, Clerici AM, Costi I, Berardinelli A, Rognone F, Savasta SM, Moglia A. Funct Neurol; 2001 Oct; 16(4):337-45. PubMed ID: 11853325 [Abstract] [Full Text] [Related]