lactic acid has been researched along with Glycogenosis in 26 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 fasting glucagon test of 40 patients with hepatic glycogen storage disease (type I, 13 patients; type Ib, 5 patients; type III, 12 patients; type IX (phosphorylase kinase deficiency), 10 patients) has been reviewed." | 7.66 | Value of the glucagon test in screening for hepatic glycogen storage disease. ( Dunger, DB; Leonard, JV, 1982) |
"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) |
"The fasting glucagon test of 40 patients with hepatic glycogen storage disease (type I, 13 patients; type Ib, 5 patients; type III, 12 patients; type IX (phosphorylase kinase deficiency), 10 patients) has been reviewed." | 3.66 | Value of the glucagon test in screening for hepatic glycogen storage disease. ( Dunger, DB; Leonard, JV, 1982) |
"The ketosis was reversed by glucagon administration." | 1.27 | Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiency. ( Brown, BI; Burke, BA; Tuchman, M; Ulstrom, RA, 1986) |
"Three patients with McArdle's disease exercised for 2 h at 30% VO2max." | 1.27 | The second wind phenomenon in McArdle's disease. ( Binkhorst, RA; Braakhekke, JP; de Bruin, MI; Joosten, EM; Stegeman, DF; Wevers, RA, 1986) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 17 (65.38) | 18.7374 |
1990's | 2 (7.69) | 18.2507 |
2000's | 3 (11.54) | 29.6817 |
2010's | 2 (7.69) | 24.3611 |
2020's | 2 (7.69) | 2.80 |
Authors | Studies |
---|---|
Serrano-Lorenzo, P | 1 |
Rabasa, M | 1 |
Esteban, J | 1 |
Hidalgo Mayoral, I | 1 |
Domínguez-González, C | 1 |
Blanco-Echevarría, A | 1 |
Garrido-Moraga, R | 1 |
Lucia, A | 1 |
Blázquez, A | 1 |
Rubio, JC | 1 |
Palma-Milla, C | 1 |
Arenas, J | 1 |
Martín, MA | 1 |
Regan, JA | 1 |
Golubski, B | 1 |
Gilbert, EB | 1 |
Sullivan, B | 1 |
McCall, SJ | 1 |
Sata, SS | 1 |
Preisler, N | 1 |
Laforêt, P | 2 |
Echaniz-Laguna, A | 1 |
Ørngreen, MC | 1 |
Lonsdorfer-Wolf, E | 1 |
Doutreleau, S | 1 |
Geny, B | 1 |
Stojkovic, T | 2 |
Piraud, M | 2 |
Petit, FM | 1 |
Vissing, J | 2 |
Petit, F | 1 |
Orngreen, MC | 1 |
Andersen, G | 1 |
Claeys, KG | 1 |
Wary, C | 1 |
Hogrel, JY | 1 |
Soggia, AP | 1 |
Correa-Giannella, ML | 1 |
Fortes, MA | 1 |
Luna, AM | 1 |
Pereira, MA | 1 |
Tarnopolsky, M | 1 |
Stevens, L | 1 |
MacDonald, JR | 1 |
Rodriguez, C | 1 |
Mahoney, D | 1 |
Rush, J | 1 |
Maguire, J | 1 |
OEI, TL | 1 |
Bröjer, JT | 1 |
Essén-Gustavsson, B | 1 |
Annandale, EJ | 1 |
Valberg, SJ | 1 |
Mineo, I | 2 |
Kono, N | 2 |
Shimizu, T | 2 |
Sumi, S | 2 |
Nonaka, K | 2 |
Tarui, S | 2 |
Slonim, AE | 1 |
Coleman, RA | 1 |
Moses, S | 1 |
Bashan, N | 1 |
Shipp, E | 1 |
Mushlin, P | 1 |
Greene, HL | 1 |
Rumpf, KW | 1 |
Wagner, H | 1 |
Kaiser, H | 1 |
Meinck, HM | 1 |
Goebel, HH | 1 |
Scheler, F | 1 |
Hagberg, JM | 1 |
Coyle, EF | 1 |
Carroll, JE | 1 |
Miller, JM | 1 |
Martin, WH | 1 |
Brooke, MH | 1 |
Dunger, DB | 1 |
Leonard, JV | 1 |
Clark, DG | 2 |
Neville, SD | 2 |
Brinkman, M | 2 |
Filsell, OH | 1 |
de Barsy, T | 1 |
Hers, HG | 1 |
Nishimura, Y | 1 |
Challiss, RA | 1 |
Leighton, B | 1 |
Wilson, S | 1 |
Thurlby, PL | 1 |
Arch, JR | 1 |
Biggemann, B | 1 |
Hilgarth, R | 1 |
Wendel, U | 1 |
Smit, GP | 1 |
Ververs, MT | 1 |
Belderok, B | 1 |
Van Rijn, M | 1 |
Berger, R | 1 |
Fernandes, J | 1 |
Tuchman, M | 1 |
Brown, BI | 1 |
Burke, BA | 1 |
Ulstrom, RA | 1 |
Braakhekke, JP | 1 |
de Bruin, MI | 1 |
Stegeman, DF | 1 |
Wevers, RA | 1 |
Binkhorst, RA | 1 |
Joosten, EM | 1 |
van Riet, W | 1 |
de Meirsman, J | 1 |
de Saedeleer, J | 1 |
Dom, R | 1 |
Carton, H | 1 |
van den Heede, J | 1 |
Bulcke, JA | 1 |
Hara, N | 1 |
Yamada, Y | 1 |
Haynes, WD | 1 |
Williams, J | 1 |
Hosking, G | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
The Effect of Triheptanoin in Adults With McArdle Disease (Glycogen Storage Disease Type V)[NCT02432768] | Phase 2 | 22 participants (Actual) | Interventional | 2015-04-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
2 reviews available for lactic acid and Glycogenosis
Article | Year |
---|---|
Glycogen storage disease.
Topics: Blood Glucose; Glucosephosphate Dehydrogenase Deficiency; Glycogen; Glycogen Storage Disease; Glycog | 1982 |
Normal metabolism and disorders of carbohydrate metabolism.
Topics: Carbohydrate Metabolism; Enzymes; Glucose; Glycogen; Glycogen Storage Disease; Glycolysis; Humans; L | 1990 |
1 trial available for lactic acid and Glycogenosis
Article | Year |
---|---|
[Type I glycogenosis: extending therapy with uncooked cornstarch].
Topics: Adolescent; Blood Glucose; Child; Child, Preschool; Combined Modality Therapy; Creatinine; Enteral N | 1986 |
23 other studies available for lactic acid and Glycogenosis
Article | Year |
---|---|
Clinical, Biochemical, and Molecular Characterization of Two Families with Novel Mutations in the
Topics: Codon, Nonsense; Dermatitis; Female; Glycogen Storage Disease; Humans; Isoenzymes; Lactate Dehydroge | 2022 |
Glycogenic Hepatopathy Causing Elevated Lactic Acid and Liver Enzymes.
Topics: Alanine Transaminase; Alkaline Phosphatase; Aspartate Aminotransferases; Blood Glucose; Diabetes Mel | 2020 |
Fat and carbohydrate metabolism during exercise in phosphoglucomutase type 1 deficiency.
Topics: Adult; Bicycling; Carbohydrate Metabolism; Exercise Test; Exercise Tolerance; Glucose; Glycogen Stor | 2013 |
Muscle glycogenosis due to phosphoglucomutase 1 deficiency.
Topics: Adult; Ammonia; Exercise; Glycogen Storage Disease; Humans; Lactic Acid; Male; Muscle, Skeletal; Mut | 2009 |
A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0.
Topics: Base Sequence; Blood Glucose; Child; Codon, Nonsense; Exons; Fasting; Female; Frameshift Mutation; G | 2010 |
Diagnostic utility of a modified forearm ischemic exercise test and technical issues relevant to exercise testing.
Topics: Adult; Ammonia; Catheterization, Peripheral; Eating; Exercise Test; Forearm; Glycogen Storage Diseas | 2003 |
Hexose monophosphate, pyruvate and lactate in the peripheral blood in glycogen-storage disease type I.
Topics: Glycogen; Glycogen Storage Disease; Hexosephosphates; Hexoses; Humans; Lactates; Lactic Acid; Pyruva | 1962 |
Proglycogen, macroglycogen, glucose, and glucose-6-phosphate concentrations in skeletal muscles of horses with polysaccharide storage myopathy performing light exercise.
Topics: Animals; Biopsy; Creatine Kinase; Female; Glucose; Glucose-6-Phosphate; Glycogen; Glycogen Storage D | 2006 |
A comparative study on glucagon effect between McArdle disease and Tarui disease.
Topics: Adult; Female; Glucagon; Glucose; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; | 1984 |
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 |
Increased ammonia production during forearm ischemic work test in McArdle's disease.
Topics: Ammonia; Forearm; Glycogen; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; Ische | 1981 |
Exercise hyperventilation in patients with McArdle's disease.
Topics: Adult; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; Hyperventilation; | 1982 |
Value of the glucagon test in screening for hepatic glycogen storage disease.
Topics: Blood Glucose; Fasting; Glucagon; Glycogen Storage Disease; Humans; Lactates; Lactic Acid; Liver Dis | 1982 |
Glycogen metabolism in the liver of the neonatal gsd/gsd and control (GSD/GSD) rat.
Topics: Animals; Animals, Newborn; Blood Glucose; Glycogen Storage Disease; Lactates; Lactic Acid; Liver Gly | 1982 |
[Lactate dehydrogenase M subunit deficiency].
Topics: Exercise Test; Glycogen Storage Disease; Glycolysis; Humans; Isoenzymes; L-Lactate Dehydrogenase; La | 1990 |
An investigation of the beta-adrenoceptor that mediates metabolic responses to the novel agonist BRL28410 in rat soleus muscle.
Topics: Animals; Dose-Response Relationship, Drug; Ethanolamines; Female; Glycogen Storage Disease; Heart Ra | 1988 |
Complex carbohydrates in the dietary management of patients with glycogenosis caused by glucose-6-phosphatase deficiency.
Topics: Adolescent; Blood Glucose; Child; Dietary Carbohydrates; Glycogen Storage Disease; Glycogen Storage | 1988 |
Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiency.
Topics: 3-Hydroxybutyric Acid; Alanine; Blood Glucose; Child, Preschool; Glycogen Storage Disease; Histocyto | 1986 |
The second wind phenomenon in McArdle's disease.
Topics: Adaptation, Physiological; Adult; Ammonia; Blood Glucose; Cardiac Output; Electromyography; Fatigue; | 1986 |
Early onset myophosphorylase deficiency (Mc Ardle's disease) with absence of myophosphorylase protein on SDS electrophoresis. The role of the ischemic forearm test.
Topics: Adult; Biopsy; Electromyography; Electrophoresis, Polyacrylamide Gel; Exercise Test; Female; Forearm | 1985 |
Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VII.
Topics: Adult; Ammonia; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Glycogen Storage | 1985 |
Effects in vivo of food deprivation and 3-mercaptopicolinate in the glycogen-storage-disease (gsd/gsd) rat.
Topics: Animals; Blood Glucose; Body Weight; Female; Food Deprivation; Glycerol; Glycogen Storage Disease; L | 1985 |
Type V glycogen storage disease.
Topics: Child; Creatine Kinase; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; L | 1985 |