92 related articles for article (PubMed ID: 414238)
1. Genetic variants of hexosaminidase deficiency.
Patrick AD
Prog Clin Biol Res; 1977; 18():147-59. PubMed ID: 414238
[No Abstract] [Full Text] [Related]
2. Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridization.
Rattazzi MC; Brown JA; Davidson RG; Shows TB
Birth Defects Orig Artic Ser; 1975; 11(3):232-5. PubMed ID: 812568
[No Abstract] [Full Text] [Related]
3. Tay-Sachs and Sandhoff diseases: an hypothesis about the primary lesion based on hexosaminidase patterns in interspecific hybrids.
Van Cong N; Weil D; Rebourcet R; Pangalos C; Frézal J
Birth Defects Orig Artic Ser; 1975; 11(3):272-5. PubMed ID: 812570
[No Abstract] [Full Text] [Related]
4. Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridization.
Rattazzi MC; Brown JA; Davidson RG; Shows TB
Cytogenet Cell Genet; 1975; 14(3-6):402-5. PubMed ID: 1192826
[No Abstract] [Full Text] [Related]
5. 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]
6. Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis.
Rattazzi MC; Brown JA; Davidson RG; Shows TB
Am J Hum Genet; 1976 Mar; 28(2):143-54. PubMed ID: 817596
[TBL] [Abstract][Full Text] [Related]
7. Editorial: The use of tears for heterozygote detection and genetic counseling.
Goldberg MF
Invest Ophthalmol; 1974 Mar; 13(3):159-60. PubMed ID: 4205146
[No Abstract] [Full Text] [Related]
8. The lipidoses: morphologic changes in the nervous system in Gaucher's disease, GM2 gangliosidoses and Niemann-Pick disease.
Arey JB
Ann Clin Lab Sci; 1975; 5(6):475-88. PubMed ID: 812418
[TBL] [Abstract][Full Text] [Related]
9. Studies in Tay-Sachs and Sandhoff's diseases. Immunologic and structural properties of hexosaminidase A and hexosaminidase B.
Beutler E; Srivastava SK
Isr J Med Sci; 1973; 9(9):1335-7. PubMed ID: 4798071
[No Abstract] [Full Text] [Related]
10. Hexosaminidases and ganglioside catabolism in the GM2-gangliosidoses.
Tallman JF
Chem Phys Lipids; 1974 Dec; 13(4):292-304. PubMed ID: 4615840
[No Abstract] [Full Text] [Related]
11. Apparent deficiency of hexosaminidase A in healthy members of a family with Tay-Sachs disease.
Navon R; Padeh B; Adam A
Am J Hum Genet; 1973 May; 25(3):287-93. PubMed ID: 4704860
[No Abstract] [Full Text] [Related]
12. [Inborn error of glycolipid metabolism].
Suzuki Y
Horumon To Rinsho; 1975 Sep; 23(9):885-91. PubMed ID: 166
[No Abstract] [Full Text] [Related]
13. Animal model of human disease: GM2 gangliosidosis.
Pierce KR; Kosanke SD; Bay WW; Bridges CH
Am J Pathol; 1976 May; 83(2):419-22. PubMed ID: 817606
[No Abstract] [Full Text] [Related]
14. Lysosomes and mental retardation.
Hirsch I
Q Rev Biol; 1972 Sep; 47(3):303-12. PubMed ID: 4563310
[No Abstract] [Full Text] [Related]
15. [Sandhoff's disease (GM2 gangliosidosis, type 2). Clinical, biochemical and anatomo-clinical study].
Vidailhet M; Neimann N; Grignon G; Hartemann P; Philippart M; Paysant P; Nabet P; Floquet J
Arch Fr Pediatr; 1973 Jan; 30(1):45-60. PubMed ID: 4721587
[No Abstract] [Full Text] [Related]
16. A study of hexosaminadases in interspecific hybrids and in GM2 gangliosidosis with a discussion on their genetic control.
Van Cong N; Weil D; Rebourcet R; Frézal J; Richard-Mollard AM
Ann Hum Genet; 1975 Jul; 39(1):111-23. PubMed ID: 810068
[TBL] [Abstract][Full Text] [Related]
17. Serum hexosaminidase activity in I-cell disease carriers.
Vidgoff J; Buist NR
Hum Genet; 1977 May; 36(3):307-16. PubMed ID: 852874
[TBL] [Abstract][Full Text] [Related]
18. Ganglioside catabolism in hexosaminidase A-deficient adults.
Tallman JF; Brady RO; Navon R; Padeh B
Nature; 1974 Nov; 252(5480):254-5. PubMed ID: 4421837
[No Abstract] [Full Text] [Related]
19. Carrier detection in Sandhoff disease.
Lowden JA; Ives EJ; Keene DL; Burton AL; Skomorowski MA; Howard F
Am J Hum Genet; 1978 Jan; 30(1):38-45. PubMed ID: 414620
[TBL] [Abstract][Full Text] [Related]
20. Identification of a possible subunit of hexosaminidase A and B.
Robinson D; Carrol M; Stirling JL
Nature; 1973 Jun; 243(5407):415-6. PubMed ID: 4743635
[No Abstract] [Full Text] [Related]
[Next] [New Search]
