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.
28. Adult-onset neuronal ceroid lipofuscinosis (Kufs disease) with autosomal dominant inheritance in Alabama. Burneo JG; Arnold T; Palmer CA; Kuzniecky RI; Oh SJ; Faught E Epilepsia; 2003 Jun; 44(6):841-6. PubMed ID: 12790899 [No Abstract] [Full Text] [Related]
29. Childhood neuronal ceroid-lipofuscinoses in Argentina. Taratuto AL; Saccoliti M; Sevlever G; Ruggieri V; Arroyo H; Herrero M; Massaro M; Fejerman N Am J Med Genet; 1995 Jun; 57(2):144-9. PubMed ID: 7668319 [TBL] [Abstract][Full Text] [Related]
30. Protracted course of juvenile ceroid lipofuscinosis associated with a novel CLN3 mutation (p.Y199X). Sarpong A; Schottmann G; Rüther K; Stoltenburg G; Kohlschütter A; Hübner C; Schuelke M Clin Genet; 2009 Jul; 76(1):38-45. PubMed ID: 19489875 [TBL] [Abstract][Full Text] [Related]
31. Refined localization of the Batten disease gene (CLN3) by haplotype and linkage disequilibrium mapping to D16S288-D16S383 and exclusion from this region of a variant form of Batten disease with granular osmiophilic deposits. Mitchison HM; O'Rawe AM; Lerner TJ; Taschner PE; Schlumpf K; D'Arigo K; de Vos N; Gormally E; Phillips HA; Thompson AD Am J Med Genet; 1995 Jun; 57(2):312-5. PubMed ID: 7668353 [TBL] [Abstract][Full Text] [Related]
32. Adult type of neuronal ceroid-lipofuscinosis with retinal involvement. Ikeda K; Kosaka K; Oyanagi S; Yamada K Clin Neuropathol; 1984; 3(6):237-9. PubMed ID: 6518685 [TBL] [Abstract][Full Text] [Related]
36. Adult neuronal ceroid lipofuscinosis (Kufs' disease). A sporadic case. Sandyk R S Afr Med J; 1981 Nov; 60(19):754-5. PubMed ID: 7302734 [TBL] [Abstract][Full Text] [Related]
37. A family with adult type ceroid lipofuscinosis (Kufs' disease) and heart muscle disease: report of two autopsy cases. Sakajiri K; Matsubara N; Nakajima T; Fukuhara N; Makifuchi T; Wakabayashi M; Oyanagi S; Kominami E Intern Med; 1995 Dec; 34(12):1158-63. PubMed ID: 8929641 [TBL] [Abstract][Full Text] [Related]
38. A novel mutation of the CLN8 gene: is there a Mediterranean phenotype? Zelnik N; Mahajna M; Iancu TC; Sharony R; Zeigler M Pediatr Neurol; 2007 Jun; 36(6):411-3. PubMed ID: 17560505 [TBL] [Abstract][Full Text] [Related]
39. [A 54-year-old man with action myoclonus, parkinsonism and epilepsy]. Yoshioka A; Saiki S; Yamaya Y; Kanemoto M; Hirose G No To Shinkei; 1999 Nov; 51(11):999-1007. PubMed ID: 10586420 [TBL] [Abstract][Full Text] [Related]
40. Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosis. Cannelli N; Nardocci N; Cassandrini D; Morbin M; Aiello C; Bugiani M; Criscuolo L; Zara F; Striano P; Granata T; Bertini E; Simonati A; Santorelli FM Neuropediatrics; 2007 Feb; 38(1):46-9. PubMed ID: 17607606 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]