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Mutations in DYT1: extension of the phenotypic and mutational spectrum.
Kabakci K, Hedrich K, Leung JC, Mitterer M, Vieregge P, Lencer R, Hagenah J, Garrels J, Witt K, Klostermann F, Svetel M, Friedman J, Kostic V, Bressman SB, Breakefield XO, Ozelius LJ, Pramstaller PP, Klein C. Kabakci K, et al. Among authors: bressman sb. Neurology. 2004 Feb 10;62(3):395-400. doi: 10.1212/01.wnl.0000113024.84178.f7. Neurology. 2004. PMID: 14872019
Human gene for torsion dystonia located on chromosome 9q32-q34.
Ozelius L, Kramer PL, Moskowitz CB, Kwiatkowski DJ, Brin MF, Bressman SB, Schuback DE, Falk CT, Risch N, de Leon D, et al. Ozelius L, et al. Among authors: bressman sb. Neuron. 1989 May;2(5):1427-34. doi: 10.1016/0896-6273(89)90188-8. Neuron. 1989. PMID: 2576373
Linkage analysis in a family with dominantly inherited torsion dystonia: exclusion of the pro-opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphisms.
Breakefield XO, Bressman SB, Kramer PL, Ozelius L, Moskowitz C, Tanzi R, Brin MF, Hobbs W, Kaufman D, Tobin A, et al. Breakefield XO, et al. Among authors: bressman sb. J Neurogenet. 1986 May;3(3):159-75. doi: 10.3109/01677068609106846. J Neurogenet. 1986. PMID: 3016220
Delayed-onset cerebellar syndrome.
Louis ED, Lynch T, Ford B, Greene P, Bressman SB, Fahn S. Louis ED, et al. Among authors: bressman sb. Arch Neurol. 1996 May;53(5):450-4. doi: 10.1001/archneur.1996.00550050080027. Arch Neurol. 1996. PMID: 8624221
164 results