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.
2. [Diagnosis of lysosomal storage diseases using ultrastructural studies and biopsies of the conjunctiva]. Libert J; Danis P Bull Mem Soc Fr Ophtalmol; 1981; 93():144-50. PubMed ID: 6809088 [No Abstract] [Full Text] [Related]
3. Sulphatases, lysosomes and disease. Roy AB Aust J Exp Biol Med Sci; 1976 Apr; 54(2):111-35. PubMed ID: 13772 [No Abstract] [Full Text] [Related]
4. [Sialidosis due to alpha-2-6 neuraminidase deficiency: a heterogeneous group]. Maroteaux P Arch Fr Pediatr; 1978 Oct; 35(8):815-8. PubMed ID: 747491 [No Abstract] [Full Text] [Related]
5. Diagnosis of myelin disorders by the biochemical analysis of tears. Van Hoof F; Campoy C Bull Soc Belge Ophtalmol; 1983 Nov; 208 Pt 1():291-5. PubMed ID: 6144340 [No Abstract] [Full Text] [Related]
10. Current concepts in genetics. Lysosomal storage diseases. Kolodny EH N Engl J Med; 1976 May; 294(22):1217-20. PubMed ID: 817200 [No Abstract] [Full Text] [Related]
11. [Neuroepidemiology of metabolism inborn errors: diseases of lysosomal origin]. Chabás A An Esp Pediatr; 1988 Sep; 29 Suppl 33():48-51. PubMed ID: 3074716 [No Abstract] [Full Text] [Related]
12. [Lysosomal enzyme deficiency and its modifying factors]. Okada S No To Shinkei; 1985 May; 37(5):514-6. PubMed ID: 3927953 [No Abstract] [Full Text] [Related]
14. [Characterization of a new type of metachromatic leukodystrophy]. Turpin JC; Dubois G; Baumann N C R Acad Hebd Seances Acad Sci D; 1974 May; 278(22):2819-22. PubMed ID: 4212575 [No Abstract] [Full Text] [Related]
15. "I-cell" disease: leakage of lysosomal enzymes into extracellular fluids. Wiesmann U; Vassella F; Herschkowitz N N Engl J Med; 1971 Nov; 285(19):1090-1. PubMed ID: 4328711 [No Abstract] [Full Text] [Related]
16. [Outlooks offered by lysosomal enzyme determination in neuropediatrics]. Turpin JC; Dubois G; Moréno P; Baumann N Arch Fr Pediatr; 1972; 29(6):674. PubMed ID: 5078373 [No Abstract] [Full Text] [Related]
17. 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]
19. [Mucolipidosis type I. Sialidosis due to alpha-2-6-neuraminidase deficiency with neurological symptoms]. Maroteaux P; Poissonnier M; Tondeur M; Strecker G; Lemonnier M Arch Fr Pediatr; 1978 Mar; 35(3):280-91. PubMed ID: 666524 [TBL] [Abstract][Full Text] [Related]