adenosine has been researched along with Developmental Disabilities 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 | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Becker, PH; Benoist, JF; Davit-Spraul, A; Demir, Z; Gaignard, P; Gonzales, E; Habes, D; Imbard, A; Jacquemin, E; Mozer Glassberg, Y; Mussini, C; Rozenfeld Bar Lev, M; Sevin, C; Slama, A; Thérond, P | 1 |
| Cui, GS; Jiang, GB; Jiang, LY; Lai, WY; Li, A; Li, W; Liu, X; Sun, BF; Tong, WM; Wang, CX; Wang, HL; Wang, M; Wang, XJ; Xu, K; Yang, Y; Yang, YG; Zhang, XX; Zhou, Q | 1 |
| Barker, PB; De Boer, L; Engelke, U; Fahrner, JA; Horská, A; Lin, DD; Maegawa, GH; Marie, S; Morava, E; Van der Graaf, M; Vining, E; Wevers, RA; Willemsen, MA; Zulfiqar, M | 1 |
3 other study(ies) available for adenosine and Developmental Disabilities
| Article | Year |
|---|---|
Adenosine kinase deficiency: Three new cases and diagnostic value of hypermethioninemia.
Topics: Adenosine; Adenosine Kinase; Amino Acid Metabolism, Inborn Errors; Child; Developmental Disabilities; Epilepsy; Female; Genetic Predisposition to Disease; Glycine N-Methyltransferase; Humans; Infant; Infant, Newborn; Liver Diseases; Male; Retrospective Studies | 2021 |
METTL3-mediated m6A modification is required for cerebellar development.
Topics: Adenosine; Alternative Splicing; Animals; Apoptosis; Cells, Cultured; Cerebellum; Developmental Disabilities; Gene Expression Regulation; Methylation; Methyltransferases; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Mice, Knockout; Nervous System Malformations; RNA Stability; RNA, Messenger | 2018 |
Novel proton MR spectroscopy findings in adenylosuccinate lyase deficiency.
Topics: Adenosine; Adenylosuccinate Lyase; Aminoimidazole Carboxamide; Autistic Disorder; Brain; Developmental Disabilities; DNA Mutational Analysis; Female; Humans; Image Enhancement; Image Interpretation, Computer-Assisted; Infant; Magnetic Resonance Spectroscopy; Male; Psychomotor Disorders; Purine-Pyrimidine Metabolism, Inborn Errors; Ribonucleosides | 2013 |