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Journal Abstract Search
149 related items for PubMed ID: 4662801
1. [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]
2. [A contribution concerning the infantile neuro-axonal dystrophy. Comparison to Hallervorden-Spatz disease regarding histopathologic findings and clinical symptoms]. Richter E. Z Neurol; 1972 Jul; 201(2):160-95. PubMed ID: 4112646 [No Abstract] [Full Text] [Related]
3. [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 Jul; 71(5):392-406. PubMed ID: 5004231 [No Abstract] [Full Text] [Related]
4. [Case of parkinsonism with degeneration of the outer globus pallidus--relationship to progressive atrophy of globus pallidus and Hallervorden-Spatz disease]. Harada K, Koike M, Tomonaga M. Rinsho Shinkeigaku; 1972 Jul; 12(7):339-45. PubMed ID: 4674768 [No Abstract] [Full Text] [Related]
5. [Myoclonic form of Hallervorden-Spatz disease. Clinical aspect simulating a subacute spongiform encephalitis]. Radermecker J, Rizzuto N. Rev Neurol (Paris); 1967 Feb; 116(2):184-8. PubMed ID: 6047744 [No Abstract] [Full Text] [Related]
6. [Juvenile spongious degeneration of the central nervous system. Its relation to Hallervorden-Spatz disease and the neuro-axonal dystrophies]. Brucher JM, Dom R, Robin A. Rev Neurol (Paris); 1968 Nov; 119(5):425-44. PubMed ID: 5715881 [No Abstract] [Full Text] [Related]
7. [Autopsy case of Hallervorden-Spatz disease: clinicopathological and biochemical study]. Takashima S, Iwata Y, Tanaka K, Kurokawa T, Takeshita K. Shinkei Kenkyu No Shimpo; 1969 Jun; 13(2):249-59. PubMed ID: 5390671 [No Abstract] [Full Text] [Related]
8. [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]
9. [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. [Pathogenesis of Hallervorden-Spatz disease-its neuropathology from viewpoint of systemic degenerative disorder and precocious senility]. Shiraki H. Shinkei Kenkyu No Shimpo; 1968 Aug; 12(2):389-413. PubMed ID: 5752596 [No Abstract] [Full Text] [Related]
11. Neuroaxonal dystrophy. A case of non pigmented type and protracted course. Thibault J. Acta Neuropathol; 1972 Aug; 21(3):232-8. PubMed ID: 5056009 [No Abstract] [Full Text] [Related]
12. Hallervorden spatz disease associated with lewy type inclusions. Bornstein B, Sandbank U, Fried Y. Confin Neurol; 1966 Aug; 27(5):397-405. PubMed ID: 5959225 [No Abstract] [Full Text] [Related]
13. Hallervorden-Spatz disease. Late infantile and adult types, report of two cases. Rozdilsky B, Cumings JN, Huston AF. Acta Neuropathol; 1968 Jan 02; 10(1):1-16. PubMed ID: 5640114 [No Abstract] [Full Text] [Related]
14. [Late Hallervorden-Spatz disease with important reticular and cerebellar participation]. Evrard E, Hariga J, Martin JJ, Reznik M. Psychiatr Neurol Neurochir; 1968 Jan 02; 71(3):243-54. PubMed ID: 5687405 [No Abstract] [Full Text] [Related]
15. [Rapid evolution of presenile dementia in a case of Hallervorden-Spatz disease]. Rizzuto N, Radermecker J. Acta Neurol (Napoli); 1967 Jan 02; 22(2):281-90. PubMed ID: 5304557 [No Abstract] [Full Text] [Related]