citrulline has been researched along with BCKD Deficiency in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (66.67) | 18.7374 |
| 1990's | 3 (25.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (8.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Belaiche, C; Haimi Cohen, Y; Haviv, R; Saada, A; Zeharia, A | 1 |
| COFFEY, VP | 1 |
| EFRON, ML; MACCREADY, RA; MOSER, HW; YOUNG, D | 1 |
| Dennis, JA; Healy, PJ | 1 |
| Dennis, JA; Healy, PJ; Moule, JF | 1 |
| Dennis, JA; Dodd, PR; Gundlach, AL; Harper, PA; Healy, PJ; Johnston, GA; Williams, SH | 1 |
| Bartmann, P; Gortner, L; Leupold, D; Pohlandt, F | 1 |
| Reavey, PC; Yadav, GC | 1 |
| Bloom, A; Spector, E; Streeter, S | 1 |
| Frimpter, GW | 1 |
| Menne, F | 1 |
| Berry, HK | 1 |
3 review(s) available for citrulline and BCKD Deficiency
| Article | Year |
|---|---|
Inherited enzyme deficiencies in livestock.
Topics: Animals; Animals, Domestic; Argininosuccinate Synthase; Cattle; Cattle Diseases; Citrulline; Enzymes; Factor XI Deficiency; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Multienzyme Complexes; Orotate Phosphoribosyltransferase; Orotidine-5'-Phosphate Decarboxylase; Porphyrias | 1993 |
Aminoacidurias due to inherited disorders of metabolism. 2.
Topics: Acidosis; Alanine; Amino Acid Metabolism, Inborn Errors; Arginase; Arginine; Carbamates; Citrulline; Dipeptides; Glutarates; Glycine; Histidine; Humans; Hydroxyproline; Hyperglycemia; Infant, Newborn; Keto Acids; Lysine; Malonates; Maple Syrup Urine Disease; Ornithine Carbamoyltransferase; Phosphotransferases; Proline; Sarcosine; Succinates; Urea; Valine | 1973 |
[Feeble mindedness caused by genetic disorders of amino acid metabolism].
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Intellectual Disability; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Sarcosine; Succinates; Transferases; Tryptophan; Valine | 1968 |
9 other study(ies) available for citrulline and BCKD Deficiency
| Article | Year |
|---|---|
Elevated plasma citrulline: look for dihydrolipoamide dehydrogenase deficiency.
Topics: Acidosis; Acidosis, Lactic; Alleles; Apathy; Biomarkers; Child; Child, Preschool; Citrulline; Dihydrolipoamide Dehydrogenase; DNA Mutational Analysis; Dried Blood Spot Testing; Early Diagnosis; Female; Glutamine; Humans; Infant; Infant, Newborn; Israel; Lethargy; Male; Maple Syrup Urine Disease; Neonatal Screening; Predictive Value of Tests; Reference Values; Retrospective Studies | 2014 |
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Fructose; Galactosemias; Histidine; Homocysteine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Vitamin B 6 Deficiency | 1964 |
A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Chemical Analysis; Chromatography; Citrulline; Glycine; Histidine; Homocysteine; Humans; Hydroxyproline; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Proline; Proteins; Renal Aminoacidurias; Urine | 1964 |
Use of hair root as a source of DNA for the detection of heterozygotes for recessive defects in cattle.
Topics: Animals; Cattle; Cattle Diseases; Citrulline; DNA; Genes, Recessive; Genetic Carrier Screening; Genetic Testing; Genotype; Hair Follicle; Leukocyte-Adhesion Deficiency Syndrome; Maple Syrup Urine Disease; Polymerase Chain Reaction; Polymorphism, Genetic; Porphyrias | 1995 |
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 |
Peritoneal dialysis in the treatment of metabolic crises caused by inherited disorders of organic and amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Citrulline; Creatinine; Female; Humans; Infant, Newborn; Male; Maple Syrup Urine Disease; Peritoneal Dialysis; Propionates; Tyrosine | 1989 |
Aminoacidopathies: a review of 3 years experience of investigations in a Kuwait hospital.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Citrulline; Cystinuria; Female; Glycine; Homocystinuria; Humans; Infant; Infant, Newborn; Kuwait; Male; Maple Syrup Urine Disease; Phenylalanine; Phenylketonurias; Proline; Tyrosine | 1988 |
Growth of establishes lymphocytes in selective media: application to studies of inborn metabolic errors and somatic mutations.
Topics: Amino Acid Metabolism, Inborn Errors; Cell Line; Citrulline; Culture Media; DNA, Viral; Galactosemias; Herpesvirus 4, Human; Humans; Hybrid Cells; Lesch-Nyhan Syndrome; Lymphocytes; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Mutation; Pentosyltransferases | 1973 |
Hereditary disorders of amino acid metabolism associated with mental deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Child, Preschool; Citrulline; Deficiency Diseases; Hartnup Disease; Homocystinuria; Humans; Intellectual Disability; Maple Syrup Urine Disease; Phenylketonurias; Succinates | 1969 |