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Journal Abstract Search
149 related items for PubMed ID: 4662801
21. Infantile neuroaxonal dystrophy and its relationship to Hallervorden-Spatz disease. Indravasu S, Dexter RA. Neurology; 1968 Jul; 18(7):693-9. PubMed ID: 5691597 [No Abstract] [Full Text] [Related]
23. [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]
28. [Infantile form of Hallervorden-Spatz disease (author's transl)]. Marin L, Martin JJ, Ceuterick C. Acta Neurol Belg; 1975 Jun; 75(6):257-66. PubMed ID: 1220521 [Abstract] [Full Text] [Related]
29. [Hallervorden-Spatz syndrome with acanthocytosis]. Köhler B. Monatsschr Kinderheilkd; 1989 Sep; 137(9):616-9. PubMed ID: 2811885 [Abstract] [Full Text] [Related]
30. [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]
31. Autopsy always teach and tell: neurodegeneration with brain iron accumulation: a case report. Gupta R, Kumar A, Sharma MC, Sarkar C, Goyal V, Bihari M. Indian J Pathol Microbiol; 2007 Oct; 50(4):792-4. PubMed ID: 18306557 [Abstract] [Full Text] [Related]