ammonium hydroxide has been researched along with Glycogen Storage Disease in 14 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Glycogen Storage Disease: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
| Excerpt | Relevance | Reference |
|---|---|---|
| "To examine metabolism during exercise in 2 patients with muscle phosphorylase kinase (PHK) deficiency and to further define the phenotype of this rare glycogen storage disease (GSD)." | 3.78 | Muscle phosphorylase kinase deficiency: a neutral metabolic variant or a disease? ( Akman, HO; Dimauro, S; Doutreleau, S; Echaniz-Laguna, A; Geny, B; Laforet, P; Lonsdorfer-Wolf, E; Orngreen, MC; Preisler, N; Vissing, J, 2012) |
| "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 | 9 (64.29) | 18.7374 |
| 1990's | 1 (7.14) | 18.2507 |
| 2000's | 3 (21.43) | 29.6817 |
| 2010's | 1 (7.14) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Stojkovic, T | 1 |
| Vissing, J | 2 |
| Petit, F | 1 |
| Piraud, M | 1 |
| Orngreen, MC | 2 |
| Andersen, G | 1 |
| Claeys, KG | 1 |
| Wary, C | 1 |
| Hogrel, JY | 1 |
| Laforêt, P | 2 |
| Preisler, N | 1 |
| Echaniz-Laguna, A | 1 |
| Lonsdorfer-Wolf, E | 1 |
| Doutreleau, S | 1 |
| Geny, B | 1 |
| Akman, HO | 1 |
| Dimauro, S | 1 |
| Tarnopolsky, M | 1 |
| Stevens, L | 1 |
| MacDonald, JR | 1 |
| Rodriguez, C | 1 |
| Mahoney, D | 1 |
| Rush, J | 1 |
| Maguire, J | 1 |
| Mowat, AP | 1 |
| Rumpf, KW | 1 |
| Wagner, H | 1 |
| Kaiser, H | 1 |
| Meinck, HM | 1 |
| Goebel, HH | 1 |
| Scheler, F | 1 |
| Badizadegan, K | 1 |
| Perez-Atayde, AR | 1 |
| Livingstone, C | 1 |
| Chinnery, PF | 1 |
| Turnbull, DM | 1 |
| Shimizu, T | 3 |
| Kono, N | 3 |
| Kiyokawa, H | 2 |
| Yamada, Y | 3 |
| Hara, N | 3 |
| Mineo, I | 3 |
| Kawachi, M | 2 |
| Nakajima, H | 1 |
| Wang, YL | 2 |
| Tarui, S | 3 |
| Braakhekke, JP | 1 |
| de Bruin, MI | 1 |
| Stegeman, DF | 1 |
| Wevers, RA | 1 |
| Binkhorst, RA | 1 |
| Joosten, EM | 1 |
| Heller, SL | 1 |
| Kaiser, KK | 1 |
| Planer, GJ | 1 |
| Hagberg, JM | 1 |
| Brooke, MH | 1 |
| Sumi, S | 1 |
| Nonaka, K | 1 |
| Holtzman, NA | 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] | |||||||
3 reviews available for ammonium hydroxide and Glycogen Storage Disease
| Article | Year |
|---|---|
Hepatic Disorders.
Topics: Adolescent; Adult; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Ammonia; Ch | 1982 |
The ischaemic lactate-ammonia test.
Topics: Ammonia; Biomarkers; Exercise; Forearm; Glycogen Storage Disease; Humans; Ischemia; Lactates; Muscle | 2001 |
Dietary treatment of inborn errors of metabolism.
Topics: Ammonia; Carbohydrate Metabolism, Inborn Errors; Diet Therapy; Female; Fructose; Galactosemias; Glyc | 1970 |
11 other studies available for ammonium hydroxide and Glycogen Storage Disease
| Article | Year |
|---|---|
Muscle glycogenosis due to phosphoglucomutase 1 deficiency.
Topics: Adult; Ammonia; Exercise; Glycogen Storage Disease; Humans; Lactic Acid; Male; Muscle, Skeletal; Mut | 2009 |
Muscle phosphorylase kinase deficiency: a neutral metabolic variant or a disease?
Topics: Adult; Aged; Ammonia; Biopsy; Carbohydrate Metabolism; Creatine Kinase; Exercise; Exercise Test; For | 2012 |
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 |
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 |
Focal glycogenosis of the liver in disorders of ureagenesis: its occurrence and diagnostic significance.
Topics: Adolescent; Ammonia; Carbamoyl-Phosphate Synthase (Ammonia); Child; Child, Preschool; Diagnosis, Dif | 1997 |
Erythrocyte glycolysis and its marked alterations by muscular exercise in type VII glycogenosis.
Topics: 2,3-Diphosphoglycerate; Adenine Nucleotides; Adenosine Monophosphate; Adenosine Triphosphate; Adoles | 1988 |
The second wind phenomenon in McArdle's disease.
Topics: Adaptation, Physiological; Adult; Ammonia; Blood Glucose; Cardiac Output; Electromyography; Fatigue; | 1986 |
Myogenic hyperuricemia. A common pathophysiologic feature of glycogenosis types III, V, and VII.
Topics: Adult; Ammonia; Glycogen Storage Disease; Glycogen Storage Disease Type III; Glycogen Storage Diseas | 1987 |
McArdle's disease with myoadenylate deaminase deficiency: observations in a combined enzyme deficiency.
Topics: Adult; Ammonia; AMP Deaminase; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Hu | 1987 |
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 |
Editorial: Portacaval anastomosis for metabolic disease.
Topics: Age Factors; Ammonia; Child; Child, Preschool; Cholesterol; Follow-Up Studies; Glycogen Storage Dise | 1974 |