These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
176 related items for PubMed ID: 4112646
21. Neuroaxonal dystrophy. A case of non pigmented type and protracted course. Thibault J. Acta Neuropathol; 1972; 21(3):232-8. PubMed ID: 5056009 [No Abstract] [Full Text] [Related]
24. [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]
25. Seitelberger's infantile neuroaxonal dystrophy. A case report. Rizzuto N, Vio M, Ghersini L, Panizzon F. Eur Neurol; 1973 Aug; 9(6):321-32. PubMed ID: 4712541 [No Abstract] [Full Text] [Related]
26. Unusual late-onset type of hallervorden-Spatz disease. Clinico-pathological study of a case presenting as parkinsonism. Jellinger K, Neumayer E. Z Neurol; 1972 Aug; 203(2):105-18. PubMed ID: 4119022 [No Abstract] [Full Text] [Related]
27. 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]
34. [A further contribution to the knowledge of the Hallervorden-Spatz disease]. Gallyas F, Környey S. Arch Psychiatr Nervenkr (1970); 1968 Jan; 212(1):33-45. PubMed ID: 5733780 [No Abstract] [Full Text] [Related]