aspartic acid has been researched along with BCKD Deficiency in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (25.00) | 18.7374 |
| 1990's | 1 (12.50) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 3 (37.50) | 24.3611 |
| 2020's | 1 (12.50) | 2.80 |
| Authors | Studies |
|---|---|
| Ahrens-Nicklas, RC; Jakher, Y; Xu, J | 1 |
| Bigler, DC; Bunce, SC; Mack, J; Moore, GJ; Morton, DH; Muelly, ER; Strauss, KA | 1 |
| Adachi, M; Aida, N; Asakura, Y; Hanakawa, J; Hasegawa, T; Muroya, K; Sato, T; Tajima, G; Tomiyasu, M | 1 |
| Calli, C; Coker, M; Gokben, S; Koroglu, O; Kultursay, N; Terek, D; Yalaz, M | 1 |
| Berry, GT; Jan, W; Kaplan, PB; Kaye, EM; Wang, ZJ; Zimmerman, RA | 1 |
| Moser, HW; Prensky, AL | 1 |
| Dennis, JA; Dodd, PR; Gundlach, AL; Harper, PA; Healy, PJ; Johnston, GA; Williams, SH | 1 |
| Barkin, E; Levy, HL | 1 |
1 review(s) available for aspartic acid and BCKD Deficiency
| Article | Year |
|---|---|
Brain Branched-Chain Amino Acids in Maple Syrup Urine Disease: Implications for Neurological Disorders.
Topics: Amino Acids, Branched-Chain; Aspartic Acid; Brain; Central Nervous System; Disease Susceptibility; Glutamic Acid; Humans; Lactic Acid; Maple Syrup Urine Disease; Metabolic Networks and Pathways; Nervous System Diseases | 2020 |
7 other study(ies) available for aspartic acid and BCKD Deficiency
| Article | Year |
|---|---|
Biochemical correlates of neuropsychiatric illness in maple syrup urine disease.
Topics: Adolescent; Adult; Affect; Anxiety; Aspartic Acid; Attention; Brain; Case-Control Studies; Child; Child, Preschool; Creatine; Depression; Female; Glutamic Acid; Humans; Impulsive Behavior; Liver Transplantation; Male; Maple Syrup Urine Disease; Prevalence; Psychomotor Agitation; Risk; Young Adult | 2013 |
Neonatal case of classic maple syrup urine disease: usefulness of (1) H-MRS in early diagnosis.
Topics: Aspartic Acid; Diagnosis, Differential; Early Diagnosis; Humans; Infant, Newborn; Lymphocytes; Male; Maple Syrup Urine Disease; Proton Magnetic Resonance Spectroscopy; Reproducibility of Results | 2014 |
Diagnostic tools of early brain disturbances in an asymptomatic neonate with maple syrup urine disease.
Topics: Aspartic Acid; Brain Diseases; Brain Waves; Consanguinity; Developmental Disabilities; Diet; Diet, Carbohydrate-Restricted; Electroencephalography; Humans; Infant, Newborn; Inositol; Lactic Acid; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Maple Syrup Urine Disease | 2013 |
MR diffusion imaging and MR spectroscopy of maple syrup urine disease during acute metabolic decompensation.
Topics: 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide); Amino Acids, Branched-Chain; Aspartic Acid; Basal Ganglia; Biomarkers; Brain Stem; Cerebellum; Cerebral Cortex; Creatine; Diffusion Magnetic Resonance Imaging; Female; Follow-Up Studies; Humans; Infant; Infant Welfare; Infant, Newborn; Ketone Oxidoreductases; Lactic Acid; Magnetic Resonance Spectroscopy; Male; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Multienzyme Complexes; Phosphocreatine; Radiography; Statistics as Topic; Time Factors | 2003 |
Changes in the amino acid composition of proteolipids of white matter during maturation of the human nervous system.
Topics: Adult; Aged; Amino Acids; Aspartic Acid; Central Nervous System; Child; Frontal Lobe; Humans; Infant; Infant, Newborn; Leucine; Lipoproteins; Maple Syrup Urine Disease; Phenylalanine; Proline; Tyrosine | 1967 |
Glutamate and gamma-aminobutyric acid neurotransmitter systems in the acute phase of maple syrup urine disease and citrullinemia encephalopathies in newborn calves.
Topics: Acute-Phase Reaction; Animals; Animals, Newborn; Aspartic Acid; Brain Diseases; Cattle; Cattle Diseases; Cerebral Cortex; Citrulline; Dizocilpine Maleate; Female; gamma-Aminobutyric Acid; Glutamates; Male; Maple Syrup Urine Disease; Neurotransmitter Agents; Receptors, GABA-A; Receptors, N-Methyl-D-Aspartate | 1992 |
Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Aspartic Acid; Biological Transport; Child; Chromatography, Ion Exchange; Cystine; Erythrocytes; Glutamates; Glutathione; Glycine; Histidine; Homocystine; Homocystinuria; Humans; Infant; Maple Syrup Urine Disease; Methionine; Ornithine; Phenylketonurias; Plasma; Renal Tubular Transport, Inborn Errors; Serine; Spectrophotometry; Threonine; Tyrosine | 1971 |