transferrin has been researched along with Lipodystrophy 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 | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Aracil, A; Artuch, R; Briones, P; Casado, M; Montero, R; Muchart, J; O'Callaghan, MM; Pérez, B; Pérez-Cerda, C; Pineda, M; Quintana, E | 1 |
1 other study(ies) available for transferrin and Lipodystrophy
Article | Year |
---|---|
Mild clinical and biochemical phenotype in two patients with PMM2-CDG (congenital disorder of glycosylation Ia).
Topics: Brain; Cerebellum; Congenital Disorders of Glycosylation; Developmental Disabilities; DNA; DNA Mutational Analysis; Female; Fibroblasts; Gait Disorders, Neurologic; Humans; Image Processing, Computer-Assisted; Infant; Isoelectric Focusing; Lipodystrophy; Magnetic Resonance Imaging; Neurologic Examination; Phenotype; Phosphotransferases (Phosphomutases); Transferrin | 2012 |