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3. New computed tomography scan finding in Hallervorden-Spatz syndrome. Van Kirk MP; Larsen PD; O'Connor PS J Clin Neuroophthalmol; 1986 Jun; 6(2):86-90. PubMed ID: 2942575 [TBL] [Abstract][Full Text] [Related]
4. A case of Hallervorden-Spatz syndrome diagnosed antemortemly. Thajeb P Chin Med J (Engl); 1993 Feb; 106(2):153-6. PubMed ID: 8504699 [TBL] [Abstract][Full Text] [Related]
5. Mineralization of the basal ganglia detected by CT in Hallervorden-Spatz syndrome. Tennison MB; Bouldin TW; Whaley RA Neurology; 1988 Jan; 38(1):154-5. PubMed ID: 3336450 [TBL] [Abstract][Full Text] [Related]
6. [Nuclear magnetic resonance in the Hallervorden-Spatz syndrome]. Vogl T; Bauer M; Seiderer M; Rath M Digitale Bilddiagn; 1984 Jun; 4(2):66-8. PubMed ID: 6467815 [TBL] [Abstract][Full Text] [Related]
7. [A case of Hallervorden-Spatz syndrome--clinical course and successive findings of brain CT]. Yamada T No To Hattatsu; 1991 Nov; 23(6):628-30. PubMed ID: 1760214 [No Abstract] [Full Text] [Related]
8. Striatal and pontocerebellar hypoperfusion in Hallervorden-Spatz syndrome. Castelnau P; Zilbovicius M; Ribeiro MJ; Hertz-Pannier L; Ogier H; Evrard P Pediatr Neurol; 2001 Aug; 25(2):170-4. PubMed ID: 11551749 [TBL] [Abstract][Full Text] [Related]
9. [Hallervorden-Spatz syndrome with acanthocytosis]. Köhler B Monatsschr Kinderheilkd; 1989 Sep; 137(9):616-9. PubMed ID: 2811885 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Hallervorden-Spatz disease with Lewy bodies]. Antoine JC; Tommasi M; Chalumeau A; Jouvet-Telinge A; Bourrat C Rev Neurol (Paris); 1985; 141(12):806-9. PubMed ID: 3008295 [TBL] [Abstract][Full Text] [Related]