Page last updated: 2024-09-04

glucagon and Orphan Diseases

glucagon has been researched along with Orphan Diseases in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's2 (66.67)2.80

Authors

AuthorsStudies
Garcia-Tsao, G; Mistry, PK1
Boujan, N; GĂ©raud, C1
Cecere, G; Franzese, A; Muzzi, G; Salerno, M; Shield, JP; Temple, KI; Valerio, G1

Other Studies

3 other study(ies) available for glucagon and Orphan Diseases

ArticleYear
Liver Transplantation for Mahvash Disease, an Inborn Error of Metabolism.
    The New England journal of medicine, 2023, Nov-23, Volume: 389, Issue:21

    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.
    Lancet (London, England), 2020, 03-21, Volume: 395, Issue:10228

    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.
    Diabetes care, 2004, Volume: 27, Issue:10

    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