pyridoxal phosphate has been researched along with Deficiency, Mental in 10 studies
Pyridoxal Phosphate: This is the active form of VITAMIN B 6 serving as a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. During transamination of amino acids, pyridoxal phosphate is transiently converted into pyridoxamine phosphate (PYRIDOXAMINE).
pyridoxal 5'-phosphate : The monophosphate ester obtained by condensation of phosphoric acid with the primary hydroxy group of pyridoxal.
Excerpt | Relevance | Reference |
---|---|---|
"Pyridoxine-dependent epilepsy is a rare autosomal recessive disorder." | 7.69 | Glutamate in pyridoxine-dependent epilepsy: neurotoxic glutamate concentration in the cerebrospinal fluid and its normalization by pyridoxine. ( Baumeister, FA; Egger, J; Gsell, W; Shin, YS, 1994) |
"Pyridoxine-dependent epilepsy is a rare autosomal recessive disorder." | 3.69 | Glutamate in pyridoxine-dependent epilepsy: neurotoxic glutamate concentration in the cerebrospinal fluid and its normalization by pyridoxine. ( Baumeister, FA; Egger, J; Gsell, W; Shin, YS, 1994) |
"Mabry syndrome is the triad of seizures, hyperphosphatasia, and mental disability." | 1.48 | Mabry Syndrome in a Child of South Asian Descent. ( Durrani, MYK; Humayun, KN; Ibrahim, SH; Sohail, AH, 2018) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 7 (70.00) | 18.7374 |
1990's | 1 (10.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Sohail, AH | 1 |
Durrani, MYK | 1 |
Ibrahim, SH | 1 |
Humayun, KN | 1 |
Albersen, M | 1 |
Bosma, M | 1 |
Jans, JJ | 1 |
Hofstede, FC | 1 |
van Hasselt, PM | 1 |
de Sain-van der Velden, MG | 1 |
Visser, G | 1 |
Verhoeven-Duif, NM | 1 |
Frimpter, GW | 2 |
Greenberg, AJ | 1 |
Hilgartner, M | 1 |
Fuchs, F | 1 |
Tada, K | 2 |
Wada, Y | 1 |
Arakawa, T | 2 |
Baumeister, FA | 1 |
Gsell, W | 1 |
Shin, YS | 1 |
Egger, J | 1 |
Coburn, SP | 2 |
Seidenberg, M | 1 |
Mahuren, JD | 1 |
Eichenwald, HF | 1 |
Fry, PC | 1 |
George, WF | 1 |
Andelman, RJ | 1 |
Yokoyama, Y | 1 |
Nakagawa, H | 1 |
Yoshida, T | 1 |
1 review available for pyridoxal phosphate and Deficiency, Mental
Article | Year |
---|---|
Nutrition and learning.
Topics: Animals; Brain; Child; Child, Preschool; Deficiency Diseases; Growth; Humans; Infant; Infant Nutriti | 1969 |
9 other studies available for pyridoxal phosphate and Deficiency, Mental
Article | Year |
---|---|
Mabry Syndrome in a Child of South Asian Descent.
Topics: Abnormalities, Multiple; Brain; Humans; Infant; Intellectual Disability; Male; Phosphorus Metabolism | 2018 |
Vitamin B6 in plasma and cerebrospinal fluid of children.
Topics: Adolescent; Anticonvulsants; Child; Child, Preschool; Chromatography, Liquid; Cross-Sectional Studie | 2015 |
Cystathioninuria: management.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Amniotic Fluid; Child; Child, Preschool; C | 1967 |
Hypervalinemia. Its metabolic lesion and therapeutic approach.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Body Weight; Chromatography, Paper; Diet Therapy; | 1967 |
Glutamate in pyridoxine-dependent epilepsy: neurotoxic glutamate concentration in the cerebrospinal fluid and its normalization by pyridoxine.
Topics: Adrenocorticotropic Hormone; Electroencephalography; Epilepsy; gamma-Aminobutyric Acid; Genes, Reces | 1994 |
Leukocyte pyridoxal phosphate and alkaline phosphatase in Down's syndrome and other retardates.
Topics: Adolescent; Adrenal Cortex Hormones; Adult; Aldehydes; Alkaline Phosphatase; Body Surface Area; Depr | 1969 |
Pyridoxal phosphate in lymphocytes, polymorphonuclear leukocytes, and platelets in Down's syndrome.
Topics: Adolescent; Adult; Blood Platelets; Carbon Radioisotopes; Down Syndrome; Female; Humans; Intellectua | 1974 |
Cystathioninuria and B6 dependency.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Child; Child, Prescho | 1969 |
Vitamin B6 dependent xanthurenic aciduria.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Aspartate Aminotransferases; Autoanalysis; | 1967 |