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.
132 related articles for article (PubMed ID: 5709854)
21. Neuropathological and neurochemical studies of three cases of sudanophilic leucodystrophy. Tsuchiya Y; Numabe T; Yokoi S Acta Neuropathol; 1970; 16(4):353-66. PubMed ID: 5496892 [No Abstract] [Full Text] [Related]
22. Long tract degeneration in familial sudanophilic leukodystrophy with prominent spheroids. Yazawa I; Nakano I; Yamada H; Oda M J Neurol Sci; 1997 Apr; 147(2):185-91. PubMed ID: 9106126 [TBL] [Abstract][Full Text] [Related]
23. The neuropathology of diseases of the white matter. Parr J Ann Clin Lab Sci; 1975; 5(3):167-75. PubMed ID: 1094903 [No Abstract] [Full Text] [Related]
24. Peculiar dysmorphic syndrome with orthochromatic leucodystrophy. Discussion of its relationship with Cockayne's syndrome and Pelizaeus-Merzbacher's disease. Martin JJ; Deberdt R; Philippart M; Van Acker KJ; Hooft C Acta Neuropathol; 1971; 18(3):224-33. PubMed ID: 5561979 [No Abstract] [Full Text] [Related]
31. Protracted form of spongy degeneration of the central nervous system (van Bogaert and Bertrand type). Adachi M; Volk BW Neurology; 1968 Nov; 18(11):1084-92. PubMed ID: 5751914 [No Abstract] [Full Text] [Related]
32. Sex-linked sudanophilic leukodystrophy with adrenocortical atrophy (so-called Schilder's disease). Report of a case and review of the literature. Sanchez JE; Lopez VF Neurology; 1976 Mar; 26(3):261-9. PubMed ID: 943055 [TBL] [Abstract][Full Text] [Related]
35. Leucodystrophy of late onset in two members of a family. Hagen D; Cole G; Proctor NS S Afr Med J; 1979 Sep; 56(11):450-2. PubMed ID: 550369 [TBL] [Abstract][Full Text] [Related]
36. The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Neuropathological study of a case. Martin JJ; Ceuterick CM; Leroy JG; Devos EA; Roelens JG Neuropediatrics; 1984 Feb; 15(1):43-8. PubMed ID: 6200796 [TBL] [Abstract][Full Text] [Related]
37. Fibrinoidal leucodystrophy (Alexander's disease) at 13 months girl. A case report. Marszał E; Kałuza J; Adamek D; Jamroz E Patol Pol; 1992; 43(4):193-5. PubMed ID: 1287550 [TBL] [Abstract][Full Text] [Related]
38. Dysmyelination in "jimpy" mouse. Electron microscopic study. Meier C; Bischoff A J Neuropathol Exp Neurol; 1974 Jul; 33(3):343-53. PubMed ID: 4835113 [No Abstract] [Full Text] [Related]
39. [Congenital familial spongy idiocy (van Bogaert-Bertrand syndrome) in a non-Jewish family (study of a 2d Italian family)]. Morcaldi L; Salvati G; Giordano GG; Guazzi GC Acta Genet Med Gemellol (Roma); 1969 Apr; 18(2):142-57. PubMed ID: 5369099 [No Abstract] [Full Text] [Related]
40. Pelizaeusmerzbacher disease "infantile acute type"; report of a family. Nisenbaum C; Sandbank U; Kohn R Ann Paediatr; 1965; 204(6):365-76. PubMed ID: 5898404 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]