glucagon has been researched along with Myoglobinuria in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
FAHN, S; ROWLAND, LP; SCHOTLAND, DL | 1 |
HARLEY, EL; KELLY, JJ; KONTOS, HA; MAGEE, JH; WASSERMAN, AJ | 1 |
Faloon, WW; Fattah, SM; Rubulis, A | 1 |
3 other study(ies) available for glucagon and Myoglobinuria
Article | Year |
---|---|
MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE.
Topics: Adenosine Triphosphate; Consanguinity; Electromyography; Genetics, Medical; Glucagon; Glycogen Storage Disease; Glycogen Storage Disease Type V; Hemoglobinuria; Hemoglobinuria, Paroxysmal; Humans; Metabolic Diseases; Muscle Cramp; Muscular Diseases; Myoglobin; Myoglobinuria; Pathology; Phosphorylase Kinase; Phosphorylases; Physical Exertion | 1963 |
EXERTIONAL IDIOPATHIC PAROXYSMAL MYOGLOBINURIA. EVIDENCE OF A DEFECT IN SKELETAL MUSCLE METABOLISM.
Topics: Biopsy; Black People; Blood Chemical Analysis; Fatigue; Glucagon; Glucose; Glucose Tolerance Test; Hemoglobinuria; Hemoglobinuria, Paroxysmal; Humans; Insulin; Metabolic Diseases; Metabolism; Muscle, Skeletal; Muscles; Muscular Atrophy; Muscular Diseases; Myoglobin; Myoglobinuria; Pain; Physical Exertion | 1963 |
McArdle's disease. Metabolic studies in a patient and review of the syndrome.
Topics: Adult; Ethanol; Fructose; Glucagon; Glucose; Glucosyltransferases; Glycogen Storage Disease; Humans; Lactates; Male; Muscles; Muscular Diseases; Myoglobinuria; Physical Exertion; Potassium | 1970 |