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Proton MR spectroscopic imaging in Pelizaeus-Merzbacher disease.
Pizzini F, Fatemi AS, Barker PB, Nagae-Poetscher LM, Horská A, Zimmerman AW, Moser HW, Bibat G, Naidu S. Pizzini F, et al. Among authors: zimmerman aw. AJNR Am J Neuroradiol. 2003 Sep;24(8):1683-9. AJNR Am J Neuroradiol. 2003. PMID: 13679292 Free PMC article.
Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2).
Hodes ME, Zimmerman AW, Aydanian A, Naidu S, Miller NR, Garcia Oller JL, Barker B, Aleck KA, Hurley TD, Dlouhy SR. Hodes ME, et al. Among authors: zimmerman aw. Am J Med Genet. 1999 Jan 15;82(2):132-9. doi: 10.1002/(sici)1096-8628(19990115)82:2<132::aid-ajmg6>3.0.co;2-4. Am J Med Genet. 1999. PMID: 9934976
Smith-Lemli-Opitz syndrome and autism spectrum disorder.
Bukelis I, Porter FD, Zimmerman AW, Tierney E. Bukelis I, et al. Among authors: zimmerman aw. Am J Psychiatry. 2007 Nov;164(11):1655-61. doi: 10.1176/appi.ajp.2007.07020315. Am J Psychiatry. 2007. PMID: 17974928 No abstract available.
106 results