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25. 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]
26. Cultured amniotic fluid cells for prenatal diagnosis of lysosomal storage disorders: a methodological study. Arnon J; Ornoy A; Bach G Prenat Diagn; 1986; 6(5):351-61. PubMed ID: 3022278 [TBL] [Abstract][Full Text] [Related]
27. Abnormal lysosomal inclusions in liver hepatocytes but not in fibroblasts in congenital disorders of glycosylation (CDG). Grünewald S; De Vos R; Jaeken J J Inherit Metab Dis; 2003; 26(1):49-54. PubMed ID: 12872840 [TBL] [Abstract][Full Text] [Related]
28. Ultrastructural studies of the skin and cultured fibroblasts in I-cell disease. Endo H; Miyazaki T; Asano S; Sagami S J Cutan Pathol; 1987 Oct; 14(5):309-17. PubMed ID: 3316329 [TBL] [Abstract][Full Text] [Related]
30. [Diagnosis of neurometabolic and neurodegenerative diseases by cutaneous biopsy]. Idoate Gastearena MA; Vega Vázquez F Rev Neurol; 1997 Sep; 25 Suppl 3():S269-80. PubMed ID: 9273173 [TBL] [Abstract][Full Text] [Related]
31. Preponderance of lysosomal bodies in cultured fibroblasts from patients with recessive epidermolysis bullosa dystrophica. An electron microscopic study. Kanan MW; Francis MJ; Sykes B; Reed WB; Ryan TJ; Van Diest P; Marsden A Br J Dermatol; 1977 May; 96(5):521-31. PubMed ID: 871388 [TBL] [Abstract][Full Text] [Related]
32. Ultrastructure of human dermal mast cells in 29 different lysosomal storage diseases. Hammel I; Alroy J; Goyal V; Galli SJ Virchows Arch B Cell Pathol Incl Mol Pathol; 1993; 64(2):83-9. PubMed ID: 8220822 [TBL] [Abstract][Full Text] [Related]
33. Investigation of tissue organelles by a combination of analytical subcellular fractionation and enzymic microanalysis: a new approach to pathology. Peters TJ J Clin Pathol; 1981 Jan; 34(1):1-12. PubMed ID: 7462432 [TBL] [Abstract][Full Text] [Related]
34. Electron microscopy: a method for the diagnosis of inherited metabolic storage diseases. Electron microscopy in diagnosis. Spycher MA Pathol Res Pract; 1980 May; 167(1):118-35. PubMed ID: 6779268 [TBL] [Abstract][Full Text] [Related]
35. [Changes in the organization of the intermediate filament system of human fibroblasts in lysosomal storage diseases and their modeling]. Ivleva TS; Tint IS; Bershadskiĭ AD; Vidershaĭn GIa Biull Eksp Biol Med; 1992 Mar; 113(3):263-8. PubMed ID: 1421222 [TBL] [Abstract][Full Text] [Related]
36. Electron microscopic examination of skin and conjunctival biopsy specimens in neuronal storage diseases. Yamano T; Shimada M; Okada S; Yutaka T; Yabuuchi H; Nakao Y Brain Dev; 1979; 1(1):16-25. PubMed ID: 233194 [TBL] [Abstract][Full Text] [Related]
37. The ultrastructure of skin from a patient with mucopolysaccharidosis IIID. Alroy J; Jones MZ; Rutledge JC; Taylor JW; Toone J; Applegarth D; Hopwood JJ Acta Neuropathol; 1997 Feb; 93(2):210-3. PubMed ID: 9039471 [TBL] [Abstract][Full Text] [Related]
38. Mitochondrial inclusions in fibroblast culture from a patient with beta-methylcrotonylglycinuria. McLean J; Stewart G J Med Genet; 1974 Sep; 11(3):257-9. PubMed ID: 4372354 [TBL] [Abstract][Full Text] [Related]
39. Accumulation of coated vesicles bearing mannose 6-phosphate receptors for lysosomal enzymes in the Golgi region of I-cell fibroblasts. Brown WJ; Farquhar MG Proc Natl Acad Sci U S A; 1984 Aug; 81(16):5135-9. PubMed ID: 6147848 [TBL] [Abstract][Full Text] [Related]
40. Problems in the application of cell culture to human genetics. Davidson RG Birth Defects Orig Artic Ser; 1974; 10(10):14-8. PubMed ID: 4618130 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]