mannose has been researched along with Microcephaly 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 | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aiello, C; Barone, R; Bertini, E; Carella, M; Concolino, D; Fiumara, A; Foulquier, F; Garozzo, D; Jaeken, J; Lefeber, DJ; Matthijs, G; Mercuri, E; Messina, S; Morava, E; Passarelli, C; Race, V; Riemersma, M; Santorelli, F; Sturiale, L; Vleugels, W; Wevers, RA | 1 |
| Filiano, J; Freeze, HH; Karnes, PS; Kim, S; Mehta, DP; Patterson, MC; Peterson, S; Srikrishna, G; Westphal, V | 1 |
2 other study(ies) available for mannose and Microcephaly
| Article | Year |
|---|---|
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy.
Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Coagulation Protein Disorders; Congenital Disorders of Glycosylation; DNA Mutational Analysis; Drug Resistance; Dystroglycans; Electromyography; Endoplasmic Reticulum; Epilepsy; Female; Fibroblasts; Glycosylation; Humans; Infant; Isoelectric Focusing; Liver Diseases; Male; Mannose; Mannosyltransferases; Microcephaly; Middle Aged; Molecular Sequence Data; Muscular Dystrophies; Mutation; Mutation, Missense; Pregnancy; Vision Disorders; Young Adult | 2012 |
Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)
Topics: Brain Diseases, Metabolic, Inborn; Carbohydrate Sequence; Cells, Cultured; Congenital Disorders of Glycosylation; Developmental Disabilities; DNA Mutational Analysis; Female; Fibroblasts; Glycoside Hydrolases; Glycosylation; Humans; Infant; Isoelectric Focusing; Isoenzymes; Male; Mannose; Mannosyltransferases; Microcephaly; Molecular Sequence Data; Mutation; Reverse Transcriptase Polymerase Chain Reaction; Seizures; Sequence Deletion; Transferrin | 2000 |