transferrin has been researched along with Child Development Deviations in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (18.18) | 18.7374 |
| 1990's | 2 (18.18) | 18.2507 |
| 2000's | 3 (27.27) | 29.6817 |
| 2010's | 4 (36.36) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aral, B; Bellanné-Chantelot, C; Blair, E; Carmignac, V; Delva, L; Donadieu, J; Droin, N; Duplomb, L; Duvet, S; El Chehadeh-Djebbar, S; Faivre, L; Foulquier, F; Gigot, N; Girodon, F; Jego, G; Klein, A; Lopez, E; Marle, N; Michalski, JC; Philippe, C; Picot, D; Rivière, JB; Solary, E; Thauvin-Robinet, C; Thevenon, J | 1 |
| Albano, R; Budetta, M; Coppola, G; D'Aniello, R; Massa, G; Papa, E; Pisano, P; Sangermano, M; Scuccimarra, G; Vajro, P | 1 |
| Balta, T; Erdogan, M; Erguven, M; Guven, S; Pala, E | 1 |
| 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 |
| Kui, LQ; Ming, QZ; Yu, T | 1 |
| Coman, D; Klingberg, S; McGill, J; Mercer, H; Morris, D | 1 |
| Gylje, H; Stibler, H; Uller, A | 1 |
| Filiano, J; Freeze, HH; Karnes, PS; Kim, S; Mehta, DP; Patterson, MC; Peterson, S; Srikrishna, G; Westphal, V | 1 |
| Hagberg, B; Kristiansson, B; Strömland, K | 1 |
| Andersson, M; Hagberg, B; Kristiansson, B; Tonnby, B | 1 |
| Jaeken, J | 1 |
11 other study(ies) available for transferrin and Child Development Deviations
| Article | Year |
|---|---|
Cohen syndrome is associated with major glycosylation defects.
Topics: Antigens, CD; Cell Adhesion Molecules; Developmental Disabilities; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Fingers; Glycosylation; Golgi Apparatus; Humans; Intellectual Disability; Intercellular Adhesion Molecule-1; Microcephaly; Muscle Hypotonia; Myopia; Obesity; Retinal Degeneration; RNA Interference; Transferrin; Vesicular Transport Proteins | 2014 |
Nutritional problems in children with neuromotor disabilities: an Italian case series.
Topics: Adolescent; Anemia, Iron-Deficiency; Body Mass Index; Cerebral Palsy; Child; Child Nutrition Disorders; Child, Preschool; Developmental Disabilities; Diet Records; Energy Intake; Epilepsy; Feeding Behavior; Female; Humans; Italy; Male; Serum Albumin; Skinfold Thickness; Transferrin; Weight Loss | 2014 |
Psychomotor development in children with iron deficiency and iron-deficiency anemia.
Topics: Aging; Anemia, Iron-Deficiency; Child; Child Development; Child, Preschool; Developmental Disabilities; Erythrocyte Indices; Ferritins; Humans; Infant; Iron; Iron Deficiencies; Parents; Prevalence; Psychomotor Disorders; Psychomotor Performance; Severity of Illness Index; Surveys and Questionnaires; Transferrin; Turkey | 2010 |
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 |
Effect of asphyxia on non-protein-bound iron and lipid peroxidation in newborn infants.
Topics: Analysis of Variance; Asphyxia Neonatorum; Bilirubin; Brain Chemistry; Case-Control Studies; Developmental Disabilities; Factor Analysis, Statistical; Female; Follow-Up Studies; Gestational Age; Hemoglobins; Humans; Infant, Newborn; Iron; Iron-Binding Proteins; Lipid Peroxidation; Male; Thiobarbituric Acid Reactive Substances; Transferrin | 2003 |
Congenital disorder of glycosylation type Ia in a 6-year-old girl with a mild intellectual phenotype: two novel PMM2 mutations.
Topics: Alleles; Carbohydrate Metabolism, Inborn Errors; Child; Developmental Disabilities; Female; Genotype; Glycosylation; Humans; Leukocytes; Mutation; Phenotype; Phosphotransferases (Phosphomutases); Time Factors; Transferrin | 2005 |
A neurodystrophic syndrome resembling carbohydrate-deficient glycoprotein syndrome type III.
Topics: Abnormalities, Multiple; Atrophy; Blotting, Western; Congenital Disorders of Glycosylation; Consanguinity; Developmental Disabilities; Female; Frontal Lobe; Glycoproteins; Humans; Infant; Limb Deformities, Congenital; Magnetic Resonance Imaging; Nails, Malformed; Nipples; Protein Isoforms; Spasms, Infantile; Syringomyelia; Transferrin | 1999 |
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 |
Ocular pathology in disialotransferrin developmental deficiency syndrome.
Topics: Adolescent; Adult; Child; Child, Preschool; Developmental Disabilities; Electroretinography; Esotropia; Female; Humans; Male; Motor Neurons; Neuromuscular Diseases; Retinitis Pigmentosa; Syndrome; Transferrin; Vision Disorders | 1990 |
Disialotransferrin developmental deficiency syndrome.
Topics: Adolescent; Adult; Asialoglycoproteins; Child; Child, Preschool; Developmental Disabilities; Facial Expression; Female; Humans; Intellectual Disability; Isoelectric Focusing; Male; Metabolism, Inborn Errors; Nervous System Diseases; Sialoglycoproteins; Syndrome; Transferrin | 1989 |
Disialotransferrin developmental deficiency syndrome and olivopontocerebellar atrophy.
Topics: Adolescent; Adult; Child; Child, Preschool; Developmental Disabilities; Humans; Metabolism, Inborn Errors; Olivopontocerebellar Atrophies; Sialic Acids; Spinocerebellar Degenerations; Syndrome; Transferrin | 1989 |