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alanine and Deficiency, Glucosephosphatase

alanine has been researched along with Deficiency, Glucosephosphatase in 8 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.

Research Excerpts

ExcerptRelevanceReference
"Seven patients with glycogen disease type I have been treated with nocturnal intragastric feeding combined with frequent daytime feeding."1.27Glycogen storage disease type I. Results of treatment with frequent daytime feeding, combined with nocturnal intragastric feeding and with administration of an alpha-glucosidase inhibitor. ( Gröbe, H; Ullrich, K, 1983)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19904 (50.00)18.7374
1990's1 (12.50)18.2507
2000's2 (25.00)29.6817
2010's1 (12.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hornemann, T1
Alecu, I1
Hagenbuch, N1
Zhakupova, A1
Cremonesi, A1
Gautschi, M1
Jung, HH1
Meienberg, F1
Bilz, S1
Christ, E1
Baumgartner, MR1
Hochuli, M1
Gröbe, H1
Ullrich, K1
Wu, MC1
Tsai, FJ1
Le, CC1
Lin, SP1
Wu, JY1
Kozák, L1
Francová, H1
Hrabincová, E1
Stastná, S1
Pesková, K1
Elleder, M1
Israels, S1
Haworth, JC1
Dunn, HG1
Applegarth, DA1
Oka, Y1
Mitsuyama, T1
Nagai, B1
Arashima, S1
Ohkubo, I1
Matsuda, I1
Collins, JE1
Bartlett, K1
Leonard, JV1
Aynsley-Green, A1
Kalderon, B1
Lapidot, A1
Korman, SH1
Gutman, A1

Reviews

1 review available for alanine and Deficiency, Glucosephosphatase

ArticleYear
Lactic acidosis in childhood.
    Advances in pediatrics, 1976, Volume: 22

    Topics: Acidosis; Alanine; Autopsy; Brain; Brain Diseases; Central Nervous System Diseases; Child; Child, Pr

1976

Other Studies

7 other studies available for alanine and Deficiency, Glucosephosphatase

ArticleYear
Disturbed sphingolipid metabolism with elevated 1-deoxysphingolipids in glycogen storage disease type I - A link to metabolic control.
    Molecular genetics and metabolism, 2018, Volume: 125, Issue:1-2

    Topics: Adolescent; Adult; Alanine; Female; Glucose; Glycogen Storage Disease Type I; Humans; Lipid Metaboli

2018
Glycogen storage disease type I. Results of treatment with frequent daytime feeding, combined with nocturnal intragastric feeding and with administration of an alpha-glucosidase inhibitor.
    European journal of pediatrics, 1983, Volume: 140, Issue:2

    Topics: Acarbose; Alanine; Aspartate Aminotransferases; Blood Glucose; Child; Enteral Nutrition; Female; Gly

1983
Identification of a novel missense mutation (T16A) in the glucose-6-phosphatase gene in a Taiwan Chinese patient with glycogen storage disease Ia (Von Gierke disease).
    Human mutation, 2000, Volume: 15, Issue:4

    Topics: Alanine; Amino Acid Substitution; Asian People; China; Glucose-6-Phosphatase; Glycogen Storage Disea

2000
Identification of mutations in the glucose-6-phosphatase gene in Czech and Slovak patients with glycogen storage disease type ia, including novel mutations K76N, V166A and 540del5.
    Human mutation, 2000, Volume: 16, Issue:1

    Topics: Alanine; Amino Acid Substitution; Asparagine; Czech Republic; Glucose-6-Phosphatase; Glycogen Storag

2000
Glucose-6-phosphatase activity in liver and blood platelets of two patients with glycogen storage disease type I.
    Clinica chimica acta; international journal of clinical chemistry, 1978, Aug-01, Volume: 87, Issue:3

    Topics: Alanine; Blood Glucose; Blood Platelets; Child, Preschool; Female; Galactose; Glucagon; Glucose-6-Ph

1978
Glucose production rates in type 1 glycogen storage disease.
    Journal of inherited metabolic disease, 1990, Volume: 13, Issue:2

    Topics: Adolescent; Adult; Alanine; Blood Glucose; Female; Glucagon; Glucose; Glycogen Storage Disease Type

1990
Glucose recycling and production in children with glycogen storage disease type I, studied by gas chromatography/mass spectrometry and (U-13C)glucose.
    Biomedical & environmental mass spectrometry, 1988, Volume: 16, Issue:1-12

    Topics: Alanine; Blood Glucose; Carbon Isotopes; Child, Preschool; Gas Chromatography-Mass Spectrometry; Glu

1988