Page last updated: 2024-10-18

glycine and Carbohydrate Metabolism, Inborn Error

glycine has been researched along with Carbohydrate Metabolism, Inborn Error in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19906 (85.71)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Glinton, KE1
Benke, PJ1
Lines, MA1
Geraghty, MT1
Chakraborty, P1
Al-Dirbashi, OY1
Jiang, Y1
Kennedy, AD1
Grotewiel, MS1
Sutton, VR1
Elsea, SH1
El-Hattab, AW1
Grøn, IH1
Gregersen, N1
Rasmussen, K1
Brady, RO1
Onisawa, J1
Lee, TY1
Levy, HL1
Duran, M1
Ketting, D1
Wadman, SK1
Trijbels, JM1
Bakkeren, JA1
Waelkens, JJ1
Thier, SO1
Alpers, DH1

Reviews

2 reviews available for glycine and Carbohydrate Metabolism, Inborn Error

ArticleYear
Genetic screening.
    Advances in human genetics, 1973, Volume: 4

    Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn

1973
Disorders of intestinal transport of amino acids.
    American journal of diseases of children (1960), 1969, Volume: 117, Issue:1

    Topics: Amino Acids; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Fructose; Galactosemias;

1969

Other Studies

5 other studies available for glycine and Carbohydrate Metabolism, Inborn Error

ArticleYear
Disturbed phospholipid metabolism in serine biosynthesis defects revealed by metabolomic profiling.
    Molecular genetics and metabolism, 2018, Volume: 123, Issue:3

    Topics: Carbohydrate Metabolism, Inborn Errors; Cell Differentiation; Child; Child, Preschool; Dietary Suppl

2018
N-Dicarboxylmonoglycines: excretion in dicarboxylic acidurias and mode of formation.
    Journal of inherited metabolic disease, 1978, Volume: 1, Issue:3

    Topics: Acyltransferases; Carbohydrate Metabolism, Inborn Errors; Dicarboxylic Acids; Gas Chromatography-Mas

1978
Inherited metabolic diseases of the nervous system.
    Science (New York, N.Y.), 1976, Aug-27, Volume: 193, Issue:4255

    Topics: Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors

1976
Biochemical studies of urinary acid mucopolysaccharide--peptide complexes in Hurler's syndrome.
    Biochemical medicine, 1970, Volume: 3, Issue:5

    Topics: Amino Acids; Aspartic Acid; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child; Child, Pr

1970
Propionic acid, an artefact which can leave methylmalonic acidemia undiscovered.
    Clinica chimica acta; international journal of clinical chemistry, 1973, Dec-12, Volume: 49, Issue:2

    Topics: Acidosis; Carbohydrate Metabolism, Inborn Errors; Chromatography, Gas; Diagnosis, Differential; Fema

1973