g(m1)-ganglioside and Mucopolysaccharidosis-VI

g(m1)-ganglioside has been researched along with Mucopolysaccharidosis-VI* in 2 studies

Reviews

1 review(s) available for g(m1)-ganglioside and Mucopolysaccharidosis-VI

Article	Year
[Factors of phenotypic polymorphism and genetic consultation in thesaurismoses (review)]. Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1980, Volume: 80, Issue:10 Topics: G(M1) Ganglioside; G(M2) Ganglioside; G(M3) Ganglioside; Gangliosidoses; Genetic Carrier Screening; Genetic Counseling; Glycoside Hydrolases; Humans; Leukodystrophy, Metachromatic; Lipidoses; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis III; Mucopolysaccharidosis IV; Mucopolysaccharidosis VI; Phenotype; Polymorphism, Genetic	1980

Article

Year

[Factors of phenotypic polymorphism and genetic consultation in thesaurismoses (review)].

Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1980, Volume: 80, Issue:10

Topics: G(M1) Ganglioside; G(M2) Ganglioside; G(M3) Ganglioside; Gangliosidoses; Genetic Carrier Screening; Genetic Counseling; Glycoside Hydrolases; Humans; Leukodystrophy, Metachromatic; Lipidoses; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis III; Mucopolysaccharidosis IV; Mucopolysaccharidosis VI; Phenotype; Polymorphism, Genetic

1980

Other Studies

1 other study(ies) available for g(m1)-ganglioside and Mucopolysaccharidosis-VI

Article	Year
Amniotic tissue transplantation as a trial of treatment in some lysosomal storage diseases. Journal of inherited metabolic disease, 1985, Volume: 8, Issue:3 This communication reports the clinical and biochemical results in six patients: four with mucopolysaccharidosis, one with GM1 gangliosidosis (Morquio B) and one with I-cell disease, who were treated by amniotic tissue transplantation. The sole evident clinical result was the diminishing of corneal clouding in three cases. A slight increase of beta-galactosidase activity in one patient's plasma was observed. The time of improvement was about 2 months after the transplantation and was transitory. Topics: Amnion; Child; Child, Preschool; Female; G(M1) Ganglioside; Gangliosidoses; Humans; Male; Mucolipidoses; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis VI	1985

Article

Year

Amniotic tissue transplantation as a trial of treatment in some lysosomal storage diseases.

Journal of inherited metabolic disease, 1985, Volume: 8, Issue:3

This communication reports the clinical and biochemical results in six patients: four with mucopolysaccharidosis, one with GM1 gangliosidosis (Morquio B) and one with I-cell disease, who were treated by amniotic tissue transplantation. The sole evident clinical result was the diminishing of corneal clouding in three cases. A slight increase of beta-galactosidase activity in one patient's plasma was observed. The time of improvement was about 2 months after the transplantation and was transitory.

Topics: Amnion; Child; Child, Preschool; Female; G(M1) Ganglioside; Gangliosidoses; Humans; Male; Mucolipidoses; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis VI

1985