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alanine and Glycogen Storage Disease

alanine has been researched along with Glycogen Storage Disease in 6 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

Glycogen Storage Disease: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.

Research Excerpts

ExcerptRelevanceReference
"The ketosis was reversed by glucagon administration."1.27Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiency. ( Brown, BI; Burke, BA; Tuchman, M; Ulstrom, RA, 1986)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19906 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Sadeghi-Nejad, A1
Hochman, H1
Senior, B1
Kreutner, W1
Springer, SC1
Sherwood, JE1
Tuchman, M1
Brown, BI1
Burke, BA1
Ulstrom, RA1
Felig, P2
Havel, RJ2
Jorfeldt, L2
Pernow, B2
Saltin, B2
Wahren, J2
Boisse, J1

Reviews

1 review available for alanine and Glycogen Storage Disease

ArticleYear
[New etiologic approach to periodic ketoacidosis in children].
    Canadian Medical Association journal, 1971, Aug-07, Volume: 105, Issue:3

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Butyrates; Carbohydrate Metabolism, Inborn Errors; Ch

1971

Other Studies

5 other studies available for alanine and Glycogen Storage Disease

ArticleYear
Studies in type I glycogenosis: the paradoxical effect of ethanol on lactate.
    The Journal of pediatrics, 1975, Volume: 86, Issue:1

    Topics: Adolescent; Adult; Alanine; Blood Glucose; Carbon Radioisotopes; Child; Chromatography; Ethanol; Fem

1975
Resistance of gluconeogenic and glycogenic pathways in obese-hyperglycemic mice.
    The American journal of physiology, 1975, Volume: 228, Issue:2

    Topics: Alanine; Animals; Enzyme Activation; Female; Genotype; Gluconeogenesis; Glucose Tolerance Test; Glyc

1975
Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiency.
    Metabolism: clinical and experimental, 1986, Volume: 35, Issue:7

    Topics: 3-Hydroxybutyric Acid; Alanine; Blood Glucose; Child, Preschool; Glycogen Storage Disease; Histocyto

1986
Amino acid metabolism during exercise in McArdle's syndrome: evidence of altered alanine metabolism.
    The Journal of physiology, 1972, Volume: 227, Issue:2

    Topics: Alanine; Amino Acids; Glucosyltransferases; Glycogen Storage Disease; Humans; Muscles; Muscular Dise

1972
Amino acid metabolism in McArdle's syndrome.
    The New England journal of medicine, 1973, Apr-12, Volume: 288, Issue:15

    Topics: Adult; Alanine; Amino Acids; Glucosyltransferases; Glycogen Storage Disease; Humans; Leg; Male; Musc

1973