leucine has been researched along with Glycogen Storage Disease Type I in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gu, Y; Qiang, W; Sun, Y; Wu, R; Yin, T; Yuan, J | 1 |
| GINSBERG, DM | 1 |
| Chan, BY; Chan, KY; Chan, YT; Chan, YW; Lam, CW; Tong, SF | 1 |
| Lee, CC; Tsai, CH; Tsai, FJ; Wu, JY; Wu, MC | 1 |
| Porath, U; Schreier, K | 1 |
2 review(s) available for leucine and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
HYPOGLYCEMIA ASSOCIATED WITH EXTRAPANCREATIC NEOPLASMS, WITH A NOTE ON OTHER UNUSUAL FORMS OF HYPOGLYCEMIA.
Topics: Adrenogenital Syndrome; Carcinoma, Hepatocellular; Drug Therapy; Glycogen Storage Disease Type I; Humans; Hypoglycemia; Leucine; Liver Glycogen; Liver Neoplasms; Mesenchymoma; Neoplasms; Retroperitoneal Neoplasms; Thoracic Neoplasms; Tolbutamide | 1964 |
[Congenital metabolic acidosis in the postnatal period].
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Fructose-1,6-Diphosphatase Deficiency; Glutarates; Glycogen Storage Disease Type I; Humans; Hyperglycemia; Infant, Newborn; Isoleucine; Ketosis; Lactates; Leucine; Leukoencephalitis, Acute Hemorrhagic; Methylmalonic Acid; Propionates; Syndrome; Thiamine; Valerates; Valine | 1978 |
3 other study(ies) available for leucine and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
A glycogen storage disease type 1a patient with type 2 diabetes.
Topics: Adenoma; Adult; Diabetes Mellitus, Type 2; Electrolytes; Female; Glucose; Glucose-6-Phosphatase; Glycogen Storage Disease Type I; Humans; Insulins; Leucine; Proline; Starch | 2022 |
A novel missense mutation (P191L) in the glucose-6-phosphate translocase gene identified in a Chinese family with glycogen storage disease 1b.
Topics: Amino Acid Substitution; Antiporters; Glycogen Storage Disease Type I; Hong Kong; Humans; Leucine; Monosaccharide Transport Proteins; Mutation, Missense; Phosphotransferases; Proline | 2000 |
A novel missense mutation (H119L) identified in a Taiwan Chinese family with glycogen storage disease Ia (Von Gierke disease).
Topics: Alternative Splicing; China; Female; Glucose-6-Phosphatase; Glycogen Storage Disease Type I; Histidine; Humans; Leucine; Male; Mutation, Missense; Nuclear Family; Taiwan | 2000 |