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.
Excerpt | Relevance | Reference |
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"Seven patients with glycogen disease type I have been treated with nocturnal intragastric feeding combined with frequent daytime feeding." | 1.27 | 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. ( Gröbe, H; Ullrich, K, 1983) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (50.00) | 18.7374 |
1990's | 1 (12.50) | 18.2507 |
2000's | 2 (25.00) | 29.6817 |
2010's | 1 (12.50) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Hornemann, T | 1 |
Alecu, I | 1 |
Hagenbuch, N | 1 |
Zhakupova, A | 1 |
Cremonesi, A | 1 |
Gautschi, M | 1 |
Jung, HH | 1 |
Meienberg, F | 1 |
Bilz, S | 1 |
Christ, E | 1 |
Baumgartner, MR | 1 |
Hochuli, M | 1 |
Gröbe, H | 1 |
Ullrich, K | 1 |
Wu, MC | 1 |
Tsai, FJ | 1 |
Le, CC | 1 |
Lin, SP | 1 |
Wu, JY | 1 |
Kozák, L | 1 |
Francová, H | 1 |
Hrabincová, E | 1 |
Stastná, S | 1 |
Pesková, K | 1 |
Elleder, M | 1 |
Israels, S | 1 |
Haworth, JC | 1 |
Dunn, HG | 1 |
Applegarth, DA | 1 |
Oka, Y | 1 |
Mitsuyama, T | 1 |
Nagai, B | 1 |
Arashima, S | 1 |
Ohkubo, I | 1 |
Matsuda, I | 1 |
Collins, JE | 1 |
Bartlett, K | 1 |
Leonard, JV | 1 |
Aynsley-Green, A | 1 |
Kalderon, B | 1 |
Lapidot, A | 1 |
Korman, SH | 1 |
Gutman, A | 1 |
1 review available for alanine and Deficiency, Glucosephosphatase
Article | Year |
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Lactic acidosis in childhood.
Topics: Acidosis; Alanine; Autopsy; Brain; Brain Diseases; Central Nervous System Diseases; Child; Child, Pr | 1976 |
7 other studies available for alanine and Deficiency, Glucosephosphatase
Article | Year |
---|---|
Disturbed sphingolipid metabolism with elevated 1-deoxysphingolipids in glycogen storage disease type I - A link to metabolic control.
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.
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).
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.
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.
Topics: Alanine; Blood Glucose; Blood Platelets; Child, Preschool; Female; Galactose; Glucagon; Glucose-6-Ph | 1978 |
Glucose production rates in type 1 glycogen storage disease.
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.
Topics: Alanine; Blood Glucose; Carbon Isotopes; Child, Preschool; Gas Chromatography-Mass Spectrometry; Glu | 1988 |