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43. Clinical and MRI study of the Hallervorden-Spatz syndrome: long-term follow-up of one case. Ou SF; Chi CS; Shian WJ; Mak SC Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1994; 35(5):439-43. PubMed ID: 7942031 [TBL] [Abstract][Full Text] [Related]
44. Clinicopathological study of familial late infantile Hallervorden-Spatz disease: a particular form of neuroacanthocytosis. Malandrini A; Fabrizi GM; Bartalucci P; Salvadori C; Berti G; Sabò C; Guazzi GC Childs Nerv Syst; 1996 Mar; 12(3):155-60. PubMed ID: 8697459 [TBL] [Abstract][Full Text] [Related]
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