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3. 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]
4. [Sandhoff disease]. Herrera Martín M; Montejo Iglesias F; Pampols T; Franquet A; Cuadrado Bello P An Esp Pediatr; 1984 Nov; 21(7):688-92. PubMed ID: 6524781 [TBL] [Abstract][Full Text] [Related]
5. [Exclusion of Sandhoff disease (Tay-Sachs 0 variant) by chorion biopsy]. Veszprémi B; Baranyai Z; Klujber L; Arany A Orv Hetil; 1992 Apr; 133(14):857-8. PubMed ID: 1522989 [TBL] [Abstract][Full Text] [Related]
6. Identification of Sandhoff disease in a Thai family: clinical and biochemical characterization. Sakpichaisakul K; Taeranawich P; Nitiapinyasakul A; Sirisopikun T J Med Assoc Thai; 2010 Sep; 93(9):1088-92. PubMed ID: 20873083 [TBL] [Abstract][Full Text] [Related]
7. [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]
14. [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]