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Tay-Sachs Disease

Known as: Hexosaminidase A deficiency, Gangliosidosis GM2, Type I, GANGLIOSIDOSIS GM2 TYPE 1 
An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis… 
National Institutes of Health

Papers overview

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2010
2010
In the last years, many Authors have dealt with the uncertainty evaluation of the measurement performed by using an analog-to… 
Review
2009
Review
2009
Although temperature-dependent sex determination (TSD) has been a ‘hot topic’ for well over 30 years, the discovery of TSD in… 
1994
1994
A new technique for high-speed trinary signed-digit (TSD) arithmetic that uses optical symbolic substitution is presented. This… 
1992
1992
To the Editor.— Baumgartner et al 1,2 have recently documented higher thyroxine, free thyroxine, and reverse triiodothyronine… 
1986
1986
Food colours were extracted from pharmaceutical preparations on an Amberlite XAD-2 resin. From the food colours retained… 
1978
1978
Using the steady-state distribution of recessive lethal gene the probability of finding the elevated frequency of Tay-Sachs (TSD… 
1975
1975
Incubation of purified hexosaminidase A with merthiolate, parahydroxymercuribenzoic acid, or silver ions resulted in the… 
1974
1974
Heterozygotes for Tay-Sachs disease can be distinguished by measuring the serum hexosaminidase activity and calculating the… 
1962
1962
Although in its sociologic implications infantile amaurotic familial idiocy (Tay-Sachs disease) bears some resemblance to other…