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10. Hallervorden-Spatz syndrome in two siblings diagnosed by clinical features and magnetic resonance imaging. Tiamkao S; Nitinavakarn B; Jitpimolmard S J Med Assoc Thai; 2000 Dec; 83(12):1535-40. PubMed ID: 11253896 [TBL] [Abstract][Full Text] [Related]
11. [Hallervorden-Spatz syndrome. Indicative findings in cranial computerized and magnetic resonance tomography for intra vitam diagnosis]. Kurlemann G; Bongartz G; Kuchelmeister K; Palm DG Monatsschr Kinderheilkd; 1991 Sep; 139(9):626-8. PubMed ID: 1745254 [TBL] [Abstract][Full Text] [Related]
13. [Importance of magnetic resonance in the diagnosis of Hallervorden- Spatz disease: presentation of a case with familial history]. Pérez Sempere A; Martínez Menéndez B; Villaverde Amundarain FJ; Calandre Hoenigsfeld L; Bermejo Pareja F Neurologia; 1990; 5(7):252-3. PubMed ID: 2288756 [No Abstract] [Full Text] [Related]
14. [Magnetic resonance tomography confirms the diagnosis of Hallervorden-Spatz disease]. Scheer PJ; Perz A; Ebner F; Kratky-Dunitz M Padiatr Padol; 1988; 23(3):245-52. PubMed ID: 3186269 [TBL] [Abstract][Full Text] [Related]
20. First cases in the Czech Republic of the Hallervorden-Spatz disease resulting from mutation in the pantothenate kinase 2 gene. Zumrová A; Krepelová A; Kyncl M; Maríková T; Prosková M; Cíbochová R; Sebronová V; Komárek V Neuro Endocrinol Lett; 2005 Jun; 26(3):213-8. PubMed ID: 15990724 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]