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2. Abnormalities of lysosomes in human diploid fibroblasts from patients with Farber's disease. Chen WW; Decker GL Biochim Biophys Acta; 1982 Oct; 718(2):185-92. PubMed ID: 6814495 [TBL] [Abstract][Full Text] [Related]
3. A family with combined Farber and Sandhoff, isolated Sandhoff and isolated fetal Farber disease: postnatal exclusion and prenatal diagnosis of Farber disease using lipid loading tests on intact cultured cells. Levade T; Enders H; Schliephacke M; Harzer K Eur J Pediatr; 1995 Aug; 154(8):643-8. PubMed ID: 7588966 [TBL] [Abstract][Full Text] [Related]
5. Considerations in the prenatal assessment of lysosomal enzyme deficiency in eight cases at risk. Carey WF; Nelson PV; Pollard AC Aust J Exp Biol Med Sci; 1977 Jun; 55(3):253-62. PubMed ID: 410399 [TBL] [Abstract][Full Text] [Related]
6. Farber's disease in two siblings, sural nerve and subcutaneous biopsies by light and electron microscopy. Pellissier JF; Berard-Badier M; Pinsard N Acta Neuropathol; 1986; 72(2):178-88. PubMed ID: 3103372 [TBL] [Abstract][Full Text] [Related]
7. Farber's lipogranulomatosis: ceramidase deficiency and prolonged survival in three relatives. Pavone L; Moser HW; Mollica F; Reitano C; Durand P Johns Hopkins Med J; 1980 Nov; 147(5):193-6. PubMed ID: 7441940 [No Abstract] [Full Text] [Related]
8. [Farber's lipogranulomatosis]. Koga M Nihon Rinsho; 1995 Dec; 53(12):3009-13. PubMed ID: 8577050 [TBL] [Abstract][Full Text] [Related]
9. A high-performance liquid chromatographic assay for acid ceramidase activity in cultured fibroblasts from patients with Farber's disease and from controls. Mitsuo K; Kobayashi T; Shinnoh N; Goto I Clin Chim Acta; 1988 Apr; 173(3):281-7. PubMed ID: 3383428 [TBL] [Abstract][Full Text] [Related]
11. Simple ultra-microtechniques for genetic complementation analysis and early prenatal diagnosis of sphingolipidoses. Hösli P Adv Exp Med Biol; 1976; 68():1-13. PubMed ID: 820166 [No Abstract] [Full Text] [Related]