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.
104 related articles for article (PubMed ID: 4209922)
1. [Method for determination of hexosaminidases A and B in leukocytes and plasma. Application to the diagnosis of gangliosidosis A GM2]. Buré J; Diebler MF; Polonovski J Ann Biol Clin (Paris); 1974; 32(1):47-51. PubMed ID: 4209922 [No Abstract] [Full Text] [Related]
2. [Enzyme diagnostics in lysosomal diseases with emphasis on sphingolipidoses]. Dreyfus JC; Poenaru L Arch Fr Pediatr; 1975; 32(6):503-14. PubMed ID: 810108 [TBL] [Abstract][Full Text] [Related]
3. [Isoenzymes of beta-N-acetyl-hexosaminidase in leukocytes]. De Virgiliis S; Biagini W; Cao A Minerva Pediatr; 1975 Apr; 27(12):719-20. PubMed ID: 1128473 [No Abstract] [Full Text] [Related]
4. Diagnosis of homozygotes and heterozygotes of GM2 gangliosidosis by hexoaminidases assay. Harteman P; Paternotte P; Vagner F; Nabet P; Paysant P Biomedicine; 1974 May; 20(3):242-8. PubMed ID: 4433658 [No Abstract] [Full Text] [Related]
5. [Sandhoff's disease: clinical and genetic study of a French-Canadian child]. Melançon SB; Potier M; Geoffroy G; Dallaire L Union Med Can; 1974 Jul; 103(7):1218-22. PubMed ID: 4210450 [No Abstract] [Full Text] [Related]
6. Heterozygote detection of type I Gaucher disease using blood platelets. Nakagawa S; Kumin S; Sachs G; Nitowsky HM Prog Clin Biol Res; 1982; 95():597-602. PubMed ID: 6812088 [No Abstract] [Full Text] [Related]
7. [Detection of carriers of Tay-Sachs disease by determining blood N-acetylhexosaminadase A activity]. Tsvetkova IV; Kozina AB Vopr Med Khim; 1974; 20(6):631-4. PubMed ID: 4450529 [No Abstract] [Full Text] [Related]
8. [The biochemical diagnosis of Gaucher disease]. Yargui L; Mokhtari S; Arab M; Berhoune A Arch Pediatr; 2005 Aug; 12(8):1301-9. PubMed ID: 15878824 [TBL] [Abstract][Full Text] [Related]
16. [Heterogeneity of inborn glycolipidoses and glycoproteinoses and their enzymologic diagnosis]. Tsvetkova IV Vopr Med Khim; 1982; 28(3):32-41. PubMed ID: 6808764 [No Abstract] [Full Text] [Related]
17. [Prenatal genetic diagnosis in a family with Tay-Sachs disease (enzyme variant B) (author's transl)]. Pilz H; Linke I; Käckell MY; Haller J; Lenard HG Dtsch Med Wochenschr; 1974 Mar; 99(12):578-80. PubMed ID: 4835528 [No Abstract] [Full Text] [Related]
18. Hexosaminidase A in tears and saliva for rapid identification of Tay-Sachs disease and its carriers. Singer JD; Cotlier E; Krimmer R Lancet; 1973 Nov; 2(7838):116-9. PubMed ID: 4128049 [No Abstract] [Full Text] [Related]
19. [Amaurotic familial idiocy within the scope of GM2-gangliosidosis. Apropos of a case of Sandhoff's disease studied on the clinical, neuropathological, enzymatic, and genetic levels]. Mounoud RL J Genet Hum; 1974 Jun; 22(2):139-83. PubMed ID: 4609324 [No Abstract] [Full Text] [Related]
20. Separation of N-acetyl- -D-hexosaminamidase-isoenzymes from human brain and leukocytes by cellulose acetate paper electrophoresis: a simple procedure for the diagnosis of Tay-Sachs disease. Klibansky C Isr J Med Sci; 1971 Sep; 7(9):1086-9. PubMed ID: 5151274 [No Abstract] [Full Text] [Related] [Next] [New Search]