Page last updated: 2024-08-22

mannose and Genetic Diseases

mannose has been researched along with Genetic Diseases in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (66.67)	18.7374
1990's	1 (33.33)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Dodds, WJ; Jolly, RD; Ruth, GR; Trauner, DB	1
Berger, R; Boonman, AM; de Jong, GJ; de Koning, TJ; De Schryver, J; Dorland, L; Duran, M; Gerwig, GJ; Poll-The, BT; van den Berg, IE; van Diggelen, OP; van Noort, WL	1
Atkins, L; Kanvfer, JN; Kolodny, EH; Littlefield, JW; Milunsky, A; Shih, VE	1

Reviews

2 review(s) available for mannose and Genetic Diseases

Article	Year
Screening for genetic diseases: principles and practice. Advances in veterinary science and comparative medicine, 1981, Volume: 25 Topics: Animals; Blood Coagulation Disorders; Breeding; Carbohydrate Metabolism, Inborn Errors; Cattle; Cattle Diseases; Cytogenetics; Dog Diseases; Dogs; Enzymes; Eye Diseases; Female; Genetic Carrier Screening; Genetic Diseases, Inborn; Genetic Testing; Male; Mannose; New Zealand; Pedigree; Porphyrias; Reference Standards	1981
Prenatal genetic diagnosis. 3. The New England journal of medicine, 1970, Dec-31, Volume: 283, Issue:27 Topics: Abortion, Induced; Acid Phosphatase; Adrenal Hyperplasia, Congenital; Amnion; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Congenital Abnormalities; Counseling; Culture Techniques; Cystic Fibrosis; Economics, Medical; Ethics, Medical; Female; Fetal Diseases; Fibroblasts; Genetic Diseases, Inborn; Glycogen Storage Disease; Heterozygote; Homozygote; Humans; Lysosomes; Mannose; Marfan Syndrome; Methods; Mucopolysaccharidoses; Muscular Dystrophies; Porphyrias; Pregnancy; Punctures; Xeroderma Pigmentosum	1970

Article

Year

Screening for genetic diseases: principles and practice.

Advances in veterinary science and comparative medicine, 1981, Volume: 25

Topics: Animals; Blood Coagulation Disorders; Breeding; Carbohydrate Metabolism, Inborn Errors; Cattle; Cattle Diseases; Cytogenetics; Dog Diseases; Dogs; Enzymes; Eye Diseases; Female; Genetic Carrier Screening; Genetic Diseases, Inborn; Genetic Testing; Male; Mannose; New Zealand; Pedigree; Porphyrias; Reference Standards

1981

Prenatal genetic diagnosis. 3.

The New England journal of medicine, 1970, Dec-31, Volume: 283, Issue:27

Topics: Abortion, Induced; Acid Phosphatase; Adrenal Hyperplasia, Congenital; Amnion; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Congenital Abnormalities; Counseling; Culture Techniques; Cystic Fibrosis; Economics, Medical; Ethics, Medical; Female; Fetal Diseases; Fibroblasts; Genetic Diseases, Inborn; Glycogen Storage Disease; Heterozygote; Homozygote; Humans; Lysosomes; Mannose; Marfan Syndrome; Methods; Mucopolysaccharidoses; Muscular Dystrophies; Porphyrias; Pregnancy; Punctures; Xeroderma Pigmentosum

1970

Other Studies

1 other study(ies) available for mannose and Genetic Diseases

Article	Year
A novel disorder of N-glycosylation due to phosphomannose isomerase deficiency. Biochemical and biophysical research communications, 1998, Apr-07, Volume: 245, Issue:1 Topics: Adolescent; Child; Congenital Disorders of Glycosylation; Female; Fructose; Genetic Diseases, Inborn; Glucose; Glycosylation; Humans; Male; Mannose; Mannose-6-Phosphate Isomerase; Phosphotransferases (Phosphomutases); Transferrin	1998

Article

Year

A novel disorder of N-glycosylation due to phosphomannose isomerase deficiency.

Biochemical and biophysical research communications, 1998, Apr-07, Volume: 245, Issue:1

Topics: Adolescent; Child; Congenital Disorders of Glycosylation; Female; Fructose; Genetic Diseases, Inborn; Glucose; Glycosylation; Humans; Male; Mannose; Mannose-6-Phosphate Isomerase; Phosphotransferases (Phosphomutases); Transferrin

1998