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6. [Adult form of GM2-gangliosidosis: a man and 2 sisters with hexosaminidase-A and -B deficiency (Sandhoff disease) and literature review]. Schnorf H; Bosshard NU; Gitzelmann R; Spycher MA; Isler P; Waespe W Schweiz Med Wochenschr; 1996 May; 126(18):757-64. PubMed ID: 8693300 [TBL] [Abstract][Full Text] [Related]
7. [Sandhoff disease or GM2 gangliosidosis, type 2. High frequency of the gene in a native population]. Dodelson de Kremer R; Molina de Levstein I Medicina (B Aires); 1980; 40(1):55-73. PubMed ID: 7432140 [No Abstract] [Full Text] [Related]
8. Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon. Der Kaloustian VM; Khoury MJ; Hallal R; Idriss ZH; Deeb ME; Wakid NW; Haddad FS Am J Hum Genet; 1981 Jan; 33(1):85-9. PubMed ID: 7468596 [TBL] [Abstract][Full Text] [Related]
10. [Sandhoff's disease (GM2 gangliosidosis, type II). Presentation of a case with a clinical and biochemical study. Carrier detection]. Rodríguez Costa T; Pampols T; Gonzalez-Sastre F; Casas Fernández C; Girós ML; Codina J; Igual L; Bleda Orríz A; Rodríguez López F An Esp Pediatr; 1984 Feb; 20(2):146-52. PubMed ID: 6712025 [TBL] [Abstract][Full Text] [Related]
11. [Genetic deficiencies of beta-N-acetylhexosaminidase A and B: Tay-Sachs and Sandhoff diseases (GM2-gangliosidosis)]. Suzuki K Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):721-7. PubMed ID: 2978703 [No Abstract] [Full Text] [Related]
12. [Late infantile and juvenile form of GM2-gangliosidosis variant B1]. Eirís J; Chabás A; Coll MJ; Castro-Gago M Rev Neurol; 1999 Sep 1-15; 29(5):435-8. PubMed ID: 10584247 [TBL] [Abstract][Full Text] [Related]
15. Segregation of Tay-Sachs and Sandhoff alleles in a non-Jewish family. Lane AB; Young E; Jenkins T Am J Hum Genet; 1980 Nov; 32(6):920-6. PubMed ID: 7446530 [TBL] [Abstract][Full Text] [Related]
16. Retinal and cerebellar changes in early fetal Sandhoff disease (GM2-gangliosidosis type 2). Nørby S; Jensen OA; Schwartz M Metab Pediatr Ophthalmol; 1980; 4(3):115-9. PubMed ID: 7453274 [No Abstract] [Full Text] [Related]
17. Prenatal diagnosis of Sandhoff disease (GM2-gangliosidosis type 2). Nørby S; Schwartz M Dan Med Bull; 1979 Nov; 26(7):353-6. PubMed ID: 527387 [No Abstract] [Full Text] [Related]