glucagon has been researched along with Orphan Diseases in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 2 (66.67) | 2.80 |
Authors | Studies |
---|---|
Garcia-Tsao, G; Mistry, PK | 1 |
Boujan, N; GĂ©raud, C | 1 |
Cecere, G; Franzese, A; Muzzi, G; Salerno, M; Shield, JP; Temple, KI; Valerio, G | 1 |
3 other study(ies) available for glucagon and Orphan Diseases
Article | Year |
---|---|
Liver Transplantation for Mahvash Disease, an Inborn Error of Metabolism.
Topics: Glucagon; Humans; Liver; Liver Transplantation; Metabolism, Inborn Errors; Neoplastic Syndromes, Hereditary; Rare Diseases | 2023 |
Neuropsychiatric symptoms, skin disease, and weight loss: necrolytic migratory erythema and a glucagonoma.
Topics: Glucagon; Glucagonoma; Humans; Male; Middle Aged; Necrolytic Migratory Erythema; Neoplasm Invasiveness; Neoplasm Staging; Pancreatectomy; Pancreatic Neoplasms; Rare Diseases; Recovery of Function; Risk Assessment; Syndrome; Treatment Outcome; Weight Loss | 2020 |
Beta-cell dysfunction in classic transient neonatal diabetes is characterized by impaired insulin response to glucose but normal response to glucagon.
Topics: Chromosome Aberrations; Chromosomes, Human, Pair 6; Diabetes Mellitus; Female; Glucagon; Glucose Tolerance Test; Humans; Infant, Newborn; Insulin; Insulin Resistance; Islets of Langerhans; Male; Pedigree; Rare Diseases; Remission, Spontaneous; Risk Assessment; Sampling Studies; Siblings | 2004 |