valine has been researched along with Froehlich's Syndrome in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (100.00) | 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 |
---|---|
Bernasconi, S; Gagliardi, PC; Repaske, DR | 1 |
1 other study(ies) available for valine and Froehlich's Syndrome
Article | Year |
---|---|
Autosomal dominant neurohypophyseal diabetes insipidus associated with a missense mutation encoding Gly23-->Val in neurophysin II.
Topics: Arginine Vasopressin; Diabetes Insipidus; DNA; Exons; Female; Glycine; Humans; Hypothalamic Diseases; Infant; Magnetic Resonance Imaging; Male; Mutation; Neurophysins; Pedigree; Pituitary Gland, Posterior; Polymerase Chain Reaction; Sequence Analysis, DNA; Valine | 1997 |