Page last updated: 2024-09-04

glucagon and Myoglobinuria

glucagon has been researched along with Myoglobinuria in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19903 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
FAHN, S; ROWLAND, LP; SCHOTLAND, DL1
HARLEY, EL; KELLY, JJ; KONTOS, HA; MAGEE, JH; WASSERMAN, AJ1
Faloon, WW; Fattah, SM; Rubulis, A1

Other Studies

3 other study(ies) available for glucagon and Myoglobinuria

ArticleYear
MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE.
    Archives of neurology, 1963, Volume: 9

    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.
    The American journal of medicine, 1963, Volume: 35

    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.
    The American journal of medicine, 1970, Volume: 48, Issue:6

    Topics: Adult; Ethanol; Fructose; Glucagon; Glucose; Glucosyltransferases; Glycogen Storage Disease; Humans; Lactates; Male; Muscles; Muscular Diseases; Myoglobinuria; Physical Exertion; Potassium

1970