isomethyleugenol has been researched along with Pseudohypoparathyroidism in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Miake, H; Moriki, Y; Uno, Y; Usui, T; Watanabe, T; Yuno, A; Zeniya, S | 1 |
| Arroyo, J; Bernal-Chico, A; Castaño, L; de Nanclares, GP; Fernández-Rebollo, E; Garin, I; Goñi, F; Lecumberri, B; Orduña, R | 1 |
| Yasuda, T | 2 |
2 review(s) available for isomethyleugenol and Pseudohypoparathyroidism
| Article | Year |
|---|---|
[Pseudohypoparathyroidism].
Topics: Chromogranins; Chromosomes, Human, Pair 20; Female; Fibrous Dysplasia, Polyostotic; Genomic Imprinting; GTP-Binding Protein alpha Subunits, Gs; Humans; Male; Methylation; Mutation; Pseudohypoparathyroidism | 2005 |
[Pseudohypoparathyroidism].
Topics: Cholecalciferol; Chromogranins; Diagnosis, Differential; Exons; GTP-Binding Protein alpha Subunits, Gs; Humans; Methylation; Mutation; Pseudohypoparathyroidism | 2006 |
2 other study(ies) available for isomethyleugenol and Pseudohypoparathyroidism
| Article | Year |
|---|---|
A 22-year-old woman with hypocalcemia and clinical features of albright hereditary osteodystrophy diagnosed with sporadic pseudohypoparathyroidism type Ib using a methylation-specific multiplex ligation-dependent probe amplification assay.
Topics: Diagnosis, Differential; DNA; Female; Genetic Testing; Humans; Hypocalcemia; Methylation; Multiplex Polymerase Chain Reaction; Pseudohypoparathyroidism; Young Adult | 2014 |
New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism.
Topics: Adult; Child, Preschool; Chromogranins; Chromosomes, Human, Pair 20; Female; GTP-Binding Protein alpha Subunits, Gs; Humans; Male; Methylation; Microsatellite Repeats; Middle Aged; Polymorphism, Single Nucleotide; Pseudohypoparathyroidism; Uniparental Disomy | 2010 |