pteridines has been researched along with Brain Diseases, Metabolic, Familial in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (80.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Veldman, A | 1 |
| Santamaria-Araujo, JA | 1 |
| Sollazzo, S | 1 |
| Pitt, J | 1 |
| Gianello, R | 1 |
| Yaplito-Lee, J | 1 |
| Wong, F | 1 |
| Ramsden, CA | 1 |
| Reiss, J | 1 |
| Cook, I | 1 |
| Fairweather, J | 1 |
| Schwarz, G | 1 |
| Johnson, JL | 1 |
| Rashed, MS | 1 |
| Saadallah, AA | 1 |
| Rahbeeni, Z | 1 |
| Eyaid, W | 1 |
| Seidahmed, MZ | 1 |
| Al-Shahwan, S | 1 |
| Salih, MA | 1 |
| Osman, ME | 1 |
| Al-Amoudi, M | 1 |
| Al-Ahaidib, L | 1 |
| Jacob, M | 1 |
| Per, H | 1 |
| Gümüş, H | 1 |
| Ichida, K | 1 |
| Cağlayan, O | 1 |
| Kumandaş, S | 1 |
| Arslanoglu, S | 1 |
| Yalaz, M | 1 |
| Gökşen, D | 1 |
| Coker, M | 1 |
| Tütüncüoglu, S | 1 |
| Akisu, M | 1 |
| Darcan, S | 1 |
| Kultursay, N | 1 |
| Ciriş, M | 1 |
| Demirtaş, E | 1 |
1 review available for pteridines and Brain Diseases, Metabolic, Familial
| Article | Year |
|---|---|
Prenatal diagnosis of molybdenum cofactor deficiency and isolated sulfite oxidase deficiency.
Topics: Adult; Brain Diseases, Metabolic, Inborn; Carbon-Carbon Lyases; Carrier Proteins; Chorionic Villi; C | 2003 |
4 other studies available for pteridines and Brain Diseases, Metabolic, Familial
| Article | Year |
|---|---|
Successful treatment of molybdenum cofactor deficiency type A with cPMP.
Topics: Brain Diseases, Metabolic, Inborn; Coenzymes; Diagnosis, Differential; Dose-Response Relationship, D | 2010 |
Determination of urinary S-sulphocysteine, xanthine and hypoxanthine by liquid chromatography-electrospray tandem mass spectrometry.
Topics: Adult; Brain Diseases, Metabolic, Inborn; Child; Child, Preschool; Chromatography, Liquid; Coenzymes | 2005 |
Molybdenum cofactor deficiency: clinical features in a Turkish patient.
Topics: Adult; Brain Diseases, Metabolic, Inborn; Coenzymes; DNA Mutational Analysis; Family Health; Female; | 2007 |
Molybdenum cofactor deficiency associated with Dandy-Walker complex.
Topics: Brain; Brain Diseases, Metabolic, Inborn; Coenzymes; Dandy-Walker Syndrome; Humans; Infant, Newborn; | 2001 |