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22. The genetic pathology of lysosomes. Hers HG, Van Hoof F. Prog Liver Dis; 1970; 3():185-205. PubMed ID: 4985552 [No Abstract] [Full Text] [Related]
23. Lysosomal storage disorder 4+1 multiplex assay for newborn screening using tandem mass spectrometry: application to a small-scale population study for five lysosomal storage disorders. Orsini JJ, Martin MM, Showers AL, Bodamer OA, Zhang XK, Gelb MH, Caggana M. Clin Chim Acta; 2012 Aug 16; 413(15-16):1270-3. PubMed ID: 22548856 [Abstract] [Full Text] [Related]
25. [Lipid histochemical studies of lysosomal lipid metabolism diseases]. Dietzmann K, Mohnike D. Acta Histochem Suppl; 1984 Aug 16; 30():211-3. PubMed ID: 6201955 [No Abstract] [Full Text] [Related]
26. [Differential diagnosis of congenital lipidoses by lipid analyses of body fluids, biopsy and autopsy tissue]. Pilz H, Heipertz R. Fortschr Neurol Psychiatr Grenzgeb; 1975 Nov 16; 43(11):602-17. PubMed ID: 53174 [Abstract] [Full Text] [Related]
27. [Interest of ultrastructural study of skin and muscle biopsies in inborn storage diseases. A report of 18 cases (author's transl)]. Bioulac P, Coquet M, Fontan D, Micheau M, Beylot C, Vital C. Ann Dermatol Venereol; 1980 Mar 16; 107(3):137-48. PubMed ID: 6266327 [Abstract] [Full Text] [Related]
28. [Animal models for inborn lysosomal storage diseases (author's transl)]. Naiki M. Jikken Dobutsu; 1977 Jan 16; 26(1):65-77. PubMed ID: 404167 [No Abstract] [Full Text] [Related]
31. Electron microscopy: a method for the diagnosis of inherited metabolic storage diseases. Electron microscopy in diagnosis. Spycher MA. Pathol Res Pract; 1980 May 16; 167(1):118-35. PubMed ID: 6779268 [Abstract] [Full Text] [Related]
37. The diagnostic value of ultrastructural studies of skin-punch biopsies and buffy coat for the early diagnosis of some neurodegenerative diseases. Wisniewski KE. Ann N Y Acad Sci; 1986 May 16; 477():285-311. PubMed ID: 3028228 [No Abstract] [Full Text] [Related]