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2. [Autopsy case of Hallervorden-Spatz syndrome with Lewy body]. Chichibu M, Oyake Y, Murone I. Shinkei Kenkyu No Shimpo; 1966 Dec; 10(4):700-7. PubMed ID: 6010161 [No Abstract] [Full Text] [Related]
10. [A family with Hallervorden-Spatz disease. (Contribution to the study of the so-called pure forms]. Myle G, Fadiloglu S. Encephale; 1967 Jun; 56(4):343-59. PubMed ID: 6057416 [No Abstract] [Full Text] [Related]
11. [Early infantile familial forms of pigmentary pallido-reticular atrophy. Critical study of the value of histopathologic criteria in the differentiation of an infantile form of Hallervorden-Spatz disease]. Fadiloglu S. Acta Neurol Belg; 1971 Jun; 71(5):392-406. PubMed ID: 5004231 [No Abstract] [Full Text] [Related]
12. [Infantile neuro-axonal dystrophy and Hallervorden-Spatz disease. Electro-clinical and anatomo-pathological and differential diagnostic aspects]. Radermecker J, Martin JJ. Bull Acad R Med Belg; 1972 Jul; 12(7):459-502. PubMed ID: 4662801 [No Abstract] [Full Text] [Related]
14. [Rapid evolution of presenile dementia in a case of Hallervorden-Spatz disease]. Rizzuto N, Radermecker J. Acta Neurol (Napoli); 1967 Jul; 22(2):281-90. PubMed ID: 5304557 [No Abstract] [Full Text] [Related]
15. Hallervorden Spatz disease. Its pathogenesis and place among the axonal dystrophies. Sacks OW, Aguilar MJ, Borwn WJ. Acta Neuropathol; 1966 Mar 04; 6(2):164-74. PubMed ID: 5963287 [No Abstract] [Full Text] [Related]
19. The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome. Baumeister FA, Auer DP, Hörtnagel K, Freisinger P, Meitinger T. Neuropediatrics; 2005 Jun 02; 36(3):221-2. PubMed ID: 15944911 [Abstract] [Full Text] [Related]
20. [Generalized infantile neuroaxonal dystrophies with pigmentation and lipophanerosis of the pallidum in concordant twins (author's transl)]. Peiffer J, Brunner N, Landolt RF, Müller G, Schlote W. Neuropadiatrie; 1976 Aug 02; 7(3):327-50. PubMed ID: 183173 [Abstract] [Full Text] [Related] Page: [Next] [New Search]