[Tay-Sachs disease]. 1974

F Novoa, and M Colombo, and J Clericus

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D008064 Lipidoses Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved. Lipidosis,Lipoidosis
D008297 Male Males
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

F Novoa, and M Colombo, and J Clericus
January 1951, Archives francaises de pediatrie,
F Novoa, and M Colombo, and J Clericus
September 2004, Archives of neurology,
F Novoa, and M Colombo, and J Clericus
January 1969, Archives of neurology,
F Novoa, and M Colombo, and J Clericus
April 1973, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde,
F Novoa, and M Colombo, and J Clericus
June 1973, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde,
F Novoa, and M Colombo, and J Clericus
January 1975, Oftalmologicheskii zhurnal,
F Novoa, and M Colombo, and J Clericus
January 1998, Ryoikibetsu shokogun shirizu,
F Novoa, and M Colombo, and J Clericus
November 1979, Indian journal of pediatrics,
F Novoa, and M Colombo, and J Clericus
January 1998, Nursing times,
F Novoa, and M Colombo, and J Clericus
February 1974, Ugeskrift for laeger,
Copied contents to your clipboard!