lactic acid has been researched along with Amylo-1,6-Glucosidase Deficiency in 4 studies
Lactic Acid: A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
2-hydroxypropanoic acid : A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The plasma glucose, insulin, glucagon, lactate and amino acid response patterns to glucose and protein meals were examined in 11 patients with type III glycogen storage disease (GSD-III)." | 3.66 | Amino acid disturbances in type III glycogenosis: differences from type I glycogenosis. ( Bashan, N; Coleman, RA; Moses, S; Mushlin, P; Shipp, E; Slonim, AE, 1983) |
| "This report presents lens opacities not previously described in patients with type I or III GSD." | 1.42 | Lens opacities in glycogenoses type I and III. ( Allegrini, D; Autelitano, A; De Cillà, S; Fogagnolo, P; Mazza, M; Montanari, C; Paci, S; Piozzi, E; Riva, E; Rossetti, L, 2015) |
| "A 10-month-old girl with glycogen storage disease type III developed recurrent severe hypoglycaemia induced by infectious mononucleosis." | 1.31 | Severe hypoglycaemia in a patient with glycogen storage disease type III induced by infectious mononucleosis. ( Hayasaka, K; Ikeda, H; Ito, A; Kato, M; Kimura, T; Okubo, M, 2001) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Allegrini, D | 1 |
| Autelitano, A | 1 |
| Fogagnolo, P | 1 |
| De Cillà, S | 1 |
| Piozzi, E | 1 |
| Mazza, M | 1 |
| Paci, S | 1 |
| Montanari, C | 1 |
| Riva, E | 1 |
| Rossetti, L | 1 |
| Slonim, AE | 1 |
| Coleman, RA | 1 |
| Moses, S | 1 |
| Bashan, N | 1 |
| Shipp, E | 1 |
| Mushlin, P | 1 |
| Greene, HL | 1 |
| Kimura, T | 1 |
| Ikeda, H | 1 |
| Kato, M | 1 |
| Ito, A | 1 |
| Okubo, M | 1 |
| Hayasaka, K | 1 |
1 review available for lactic acid and Amylo-1,6-Glucosidase Deficiency
| Article | Year |
|---|---|
Glycogen storage disease.
Topics: Blood Glucose; Glucosephosphate Dehydrogenase Deficiency; Glycogen; Glycogen Storage Disease; Glycog | 1982 |
3 other studies available for lactic acid and Amylo-1,6-Glucosidase Deficiency
| Article | Year |
|---|---|
Lens opacities in glycogenoses type I and III.
Topics: Adolescent; Adult; Cataract; Creatine Kinase; Female; Glycogen Storage Disease Type I; Glycogen Stor | 2015 |
Amino acid disturbances in type III glycogenosis: differences from type I glycogenosis.
Topics: Adolescent; Adult; Amino Acids; Blood Glucose; Child; Child, Preschool; Diagnosis, Differential; Fem | 1983 |
Severe hypoglycaemia in a patient with glycogen storage disease type III induced by infectious mononucleosis.
Topics: Female; Glycogen Storage Disease Type III; Humans; Hypoglycemia; Infant; Infectious Mononucleosis; L | 2001 |