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4. Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene. Eksandh LB; Ponjavic VB; Munroe PB; Eiberg HE; Uvebrant PE; Ehinger BE; Mole SE; Andréasson S Ophthalmic Genet; 2000 Jun; 21(2):69-77. PubMed ID: 10916181 [TBL] [Abstract][Full Text] [Related]
5. Lipid peroxidation in platelets from patients with Spielmeyer-Vogt-Batten syndrome. Plum CM; Nielsen A Eur J Pediatr; 1978 Mar; 127(3):205-10. PubMed ID: 648542 [TBL] [Abstract][Full Text] [Related]
6. Renal handling of free amino acids in normal adults, in patients with epilepsy, and in patients with Spielmeyer-Vogt-Batten disease. Plum CM Dan Med Bull; 1975 Jul; 22(5):194-201. PubMed ID: 1164852 [No Abstract] [Full Text] [Related]
7. Lipoyl dehydrogenase activity of erythrocytes in Spielmeyer-Vogt-Batten's disease. Plum CM Acta Med Okayama; 1977 Aug; 31(4):249-55. PubMed ID: 145161 [TBL] [Abstract][Full Text] [Related]
8. [Case report: a family with juvenile amaurotic idiocy (Vogt-Spielmeyer). Detection of heterozygous carriers]. Klein D; Hussels I J Genet Hum; 1967 Jun; 16(1):226-31. PubMed ID: 5592428 [No Abstract] [Full Text] [Related]
9. Juvenile cerebroretinal degeneration (Spielmeyer-Vogt). Blood and EEG findings in a family of ten members. HARLEM OK Am J Dis Child; 1960 Dec; 100():918-23. PubMed ID: 13711599 [No Abstract] [Full Text] [Related]
10. Spielmeyer-Vogt syndrome, report of a case. Lindemann R; Gregg W J Oral Med; 1979; 34(4):120-1. PubMed ID: 293403 [No Abstract] [Full Text] [Related]
11. [On a case of familial amaurotic idiocy in its juvenile form (Spielmeyer-Vogt disease)]. BRAGE D; GARIBALDI DM; MENDIONDO E Rev Clin Esp; 1963 Mar; 88():341-5. PubMed ID: 14014865 [No Abstract] [Full Text] [Related]
13. Deficient leukocyte peroxidase activity in the Batten-Spielmeyer-Vogt syndrome. Armstrong D; Dimmitt S; Grider L; Van Wormer D; Austin J Trans Am Neurol Assoc; 1973; 98():3-7. PubMed ID: 4784972 [No Abstract] [Full Text] [Related]
14. Cerebro-retinal degeneration. Clinical and histopathological study. Joshua GE; Bhakthaviziam A; Jadhav M; Mathai KV Indian Pediatr; 1970 Aug; 7(8):418-28. PubMed ID: 5492569 [No Abstract] [Full Text] [Related]
15. Juvenile heredo familial lipidosis (Spielmeyer-Vogt): an electron microscopic study. Joshua GE; Bhaktaviziam A; Job CK; Basu DK Indian J Med Res; 1973 Sep; 61(9):1319-24. PubMed ID: 4779305 [No Abstract] [Full Text] [Related]
16. Neurophysiological studies in Batten's disease. Green JB Trans Am Neurol Assoc; 1971; 96():246-7. PubMed ID: 5159094 [No Abstract] [Full Text] [Related]
17. Studies on the occurrence of guanidino compounds in serum and urine of patients with epilepsy and patients with Spielmeyer-Vogt-Batten's syndrome. Plum CM Dan Med Bull; 1980 Sep; 27(4):207-11. PubMed ID: 7438808 [No Abstract] [Full Text] [Related]
18. Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosis. Chang B; Bronson RT; Hawes NL; Roderick TH; Peng C; Hageman GS; Heckenlively JR Invest Ophthalmol Vis Sci; 1994 Mar; 35(3):1071-6. PubMed ID: 8125718 [TBL] [Abstract][Full Text] [Related]
19. Spielmeyer-Vogt's disease--a case report. Meire F; De Laey JJ; Standaert L Bull Soc Belge Ophtalmol; 1984; 210():87-91. PubMed ID: 6545518 [No Abstract] [Full Text] [Related]
20. [2 familial cases of tapetoretinal degeneration (1 complicated by retinal detachment) associated with chronic tubulo-intestitial kidney disease]. Metge P; Tassy A; Arneodo J; Olmer M; Pierron H; Salvadori JM Bull Soc Ophtalmol Fr; 1971 Jan; 71(1):76-9. PubMed ID: 5315597 [No Abstract] [Full Text] [Related] [Next] [New Search]