mannose has been researched along with Hamartoma in 1 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 | 0 (0.00) | 24.3611 |
2020's | 1 (100.00) | 2.80 |
Authors | Studies |
---|---|
Akula, SK; AttiƩ-Bitach, T; de Brouwer, APM; Duvet, S; Fortuna, AM; Foulquier, F; Gheldof, A; Jansen, AC; Jorge, P; Lai, A; Loget, P; Maia, N; Nassogne, MC; O'Kane, K; Potelle, S; Proisy, M; Quelin, C; Schulz, C; Sermon, K; Soares, AR; Stouffs, K; Van Schaftingen, E; Walsh, CA; Wiame, E; Yildirim, H | 1 |
1 other study(ies) available for mannose and Hamartoma
Article | Year |
---|---|
Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorder.
Topics: Adolescent; Alleles; alpha-Mannosidase; Brain Stem; Cell Line, Tumor; Central Nervous System Cysts; Cerebellar Vermis; Child; Child, Preschool; Congenital Disorders of Glycosylation; Female; Fetus; Glycosylation; Hamartoma; Humans; Hypothalamus; Intellectual Disability; Leukocytes; Male; Mannose; Oligosaccharides; Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase; Polymicrogyria; Tongue | 2022 |