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24. [The Hallervorden-Spatz sickness with reticular and cerebellar participation in the aged]. Evrard E; Hariga J; Martin JJ; Reznik M Rev Neurol (Paris); 1967 Jun; 116(6):693. PubMed ID: 5619764 [No Abstract] [Full Text] [Related]
25. 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]
26. Psychotic disorder in a case with Hallervorden-Spatz disease. Oner O; Oner P; Deda G; Içağasioğlu D Acta Psychiatr Scand; 2003 Nov; 108(5):394-7; discussion 397-8. PubMed ID: 14531762 [TBL] [Abstract][Full Text] [Related]
30. [On a pigmentary dystrophy of reticulo-dentato-nigric and cutaneo-meningeal predilection with disseminated nodular proliferative angiomatosis. (Its relation to Hallervorden-Spatz disease, its place in the cutaneo-neuraxic pigmentary syndromes)]. van Bogaert L; Colle G Rev Neurol (Paris); 1967 Nov; 117(5):613-25. PubMed ID: 4880846 [No Abstract] [Full Text] [Related]
31. Neurodegeneration with brain iron accumulation: clinical, radiographic and genetic heterogeneity and corresponding therapeutic options. Clement F; Devos D; Moreau C; Coubes P; Destee A; Defebvre L Acta Neurol Belg; 2007 Mar; 107(1):26-31. PubMed ID: 17569231 [TBL] [Abstract][Full Text] [Related]
32. Clinical features of neuroleptic malignant syndrome in basal ganglia disease. Spontaneous presentation in a patient with Hallervorden-Spatz disease in the absence of neuroleptic drugs. Hayashi K; Chihara E; Sawa T; Tanaka Y Anaesthesia; 1993 Jun; 48(6):499-502. PubMed ID: 8322990 [TBL] [Abstract][Full Text] [Related]
34. [A family with Hallervorden-Spatz disease. (Contribution to the study of the so-called pure forms]. Myle G; Fadiloglu S Encephale; 1967; 56(4):343-59. PubMed ID: 6057416 [No Abstract] [Full Text] [Related]
35. Iron in the Hallervorden-Spatz syndrome. Koeppen AH; Dickson AC Pediatr Neurol; 2001 Aug; 25(2):148-55. PubMed ID: 11551745 [TBL] [Abstract][Full Text] [Related]
36. [A 75-year-old man with parkinsonism and sudden death]. Nagaoka M; Nakamura N; Yamamura A; Mori H; Shirai T; Mizuno Y No To Shinkei; 1995 Dec; 47(12):1199-208. PubMed ID: 8534559 [TBL] [Abstract][Full Text] [Related]
37. Hallervorden-Spatz disease. Boyacigil S; Tokoğlu F; Paşaoğlu E; Ardiç S; Comoğlu S; Saka M; Oztürk S Australas Radiol; 1996 Aug; 40(3):351-3. PubMed ID: 8826751 [TBL] [Abstract][Full Text] [Related]
39. [Hallervorden-Spatz disease in a brother and a sister (hereditary-familial fragility of the extrapyramidal apparatus)]. de Barsy T J Genet Hum; 1968 Jan; 16(3):41-7. PubMed ID: 5710711 [No Abstract] [Full Text] [Related]