arginine vasopressin has been researched along with De Morsier Syndrome in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Allegri, AE; Bertelli, E; Calcagno, A; di Iorgi, N; Gastaldi, R; Maghnie, M; Napoli, F; Olivieri, I; Pala, G; Parodi, S; Rossi, A; Secco, A | 1 |
Alatzoglou, KS; Dattani, MT; Farooqi, IS; Gaston-Massuet, C; Gerrelli, D; Gregory, LC; Kavanaugh, SI; Martinez-Barbera, JP; McCabe, MJ; Pitteloud, N; Puelles, E; Raza, J; Signore, M; Tsai, PS; Tziaferi, V; Walker, J | 1 |
2 other study(ies) available for arginine vasopressin and De Morsier Syndrome
Article | Year |
---|---|
Posterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia.
Topics: Adolescent; Arginine Vasopressin; Choristoma; Female; Humans; Hypopituitarism; Hypothalamus; Magnetic Resonance Imaging; Male; Osmolar Concentration; Pituitary Gland, Posterior; Prospective Studies; Saline Solution, Hypertonic; Septo-Optic Dysplasia; Thirst; Water-Electrolyte Imbalance | 2011 |
Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction.
Topics: Agenesis of Corpus Callosum; Arginine Vasopressin; Craniofacial Abnormalities; DNA Mutational Analysis; Female; Fibroblast Growth Factor 8; Holoprosencephaly; Human Growth Hormone; Humans; Hydrocortisone; Hypothalamic Diseases; Hypothalamo-Hypophyseal System; Immunohistochemistry; In Situ Hybridization; Infant; Magnetic Resonance Imaging; Mutation; Pituitary Diseases; Pituitary Gland; Prosencephalon; Receptor, Fibroblast Growth Factor, Type 1; Septo-Optic Dysplasia; Thyrotropin | 2011 |