citrulline has been researched along with Deficiency, Mental in 31 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 26 (83.87) | 18.7374 |
| 1990's | 3 (9.68) | 18.2507 |
| 2000's | 1 (3.23) | 29.6817 |
| 2010's | 1 (3.23) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Coppus, AM; Fekkes, D; Tuinier, S; van Duijn, CM; Verhoeven, WM | 1 |
| FREYCON, F; FREYCON, MT | 1 |
| COFFEY, VP | 1 |
| EFRON, ML; MACCREADY, RA; MOSER, HW; YOUNG, D | 1 |
| MCMURRAY, WC; MOHYUDDIN, F; RATHBUN, JC | 2 |
| Bachmann, C | 1 |
| Brown, H; Diamond, R; Efron, ML; Moser, HW; Neumann, CG | 1 |
| Armstrong, MD; Robinow, M | 1 |
| Barness, LA; Efron, ML; Morrow, G | 1 |
| Batshaw, ML; Brusilow, S; Painter, MJ; Schafer, IA; Sproul, GT; Thomas, GH | 1 |
| Brusilow, SW; Clissold, DB; Maestri, NE | 1 |
| Alonso, EM; Boyle, JT; Emond, JC; Millis, JM; Molleston, JP; Rosenthal, P; Whitington, PF | 1 |
| Nakao, T; Oyanagi, K; Sogawa, H | 1 |
| Nakao, T; Orii, T; Oyanagi, K; Sato, S; Sogawa, H | 1 |
| Nishi, N; Nishioka, N; Saito, Y; Suwa, N; Takahata, N | 1 |
| Stern, J | 1 |
| Brusilow, SW; Elliott, GR; Johnston, K; Rubenstein, JL | 1 |
| Gordon, BA; Haust, MD | 1 |
| Batshaw, ML | 1 |
| Gaffuri, G | 1 |
| Brenton, DP; Cusworth, DC; Hartley, S; Kuzemko, JA; Lumley, S | 1 |
| Cedrola, G; Guazzi, GC; Ragonese, G; Striano, S; Tancredi, F | 1 |
| Fell, V; Pollitt, RJ; Sampson, GA; Wright, T | 1 |
| Menne, F | 1 |
| Higgins, JV; Kohrman, AF; Scott-Emuakpor, A | 1 |
| Berry, HK | 1 |
| DeHackbeil, KF; Lis, AW; Lis, EW | 1 |
| Efron, ML; Moser, HW; Shih, VE | 1 |
| Dolan, TF; Nelligan, DJ; Shih, VE; Solitare, GB | 1 |
3 review(s) available for citrulline and Deficiency, Mental
| Article | Year |
|---|---|
[CITRULLINURIA].
Topics: Amino Acid Metabolism, Inborn Errors; Child; Citrulline; Citrullinemia; Humans; Infant; Intellectual Disability; Kidney; Renal Aminoacidurias; Urologic Diseases | 1963 |
Arginnosuccinic aciduria.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; Arginine; Blood Urea Nitrogen; Child, Preschool; Citrulline; Humans; Intellectual Disability; Lyases; Rats; Succinates | 1967 |
[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 |
28 other study(ies) available for citrulline and Deficiency, Mental
| Article | Year |
|---|---|
Plasma levels of nitric oxide related amino acids in demented subjects with Down syndrome are related to neopterin concentrations.
Topics: Alzheimer Disease; Amino Acids; Amino Acids, Aromatic; Amino Acids, Branched-Chain; Arginine; Citrulline; Cohort Studies; Dementia; Depression; Down Syndrome; Epilepsy; Female; Humans; Intellectual Disability; Male; Middle Aged; Neopterin; Nitric Oxide; Oxidative Stress; Severity of Illness Index | 2010 |
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 |
CITRULLINURIA.
Topics: Amino Acid Metabolism, Inborn Errors; Citrulline; Citrullinemia; Clinical Enzyme Tests; Humans; Infant; Intellectual Disability; Ligases; Metabolism; Urea | 1964 |
Long-term outcome of patients with urea cycle disorders and the question of neonatal screening.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Argininosuccinic Acid; Child; Citrulline; Diet; False Positive Reactions; Humans; Hyperammonemia; Infant, Newborn; Intellectual Disability; Metabolism, Inborn Errors; Neonatal Screening; Retrospective Studies; Treatment Outcome; Urea | 2003 |
Studies on amino acid metabolism in citrullinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Blood Chemical Analysis; Caseins; Child; Citrulline; Diet Therapy; Humans; Infant; Intellectual Disability; Ligases; Male; Neomycin; Urea | 1967 |
Argininosuccinic aciduria. Report of two new cases and demonstration of intermittent elevation of blood ammonia.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Arginine; Chromatography, Paper; Citrulline; Electroencephalography; Electrophoresis; Female; Humans; Intellectual Disability; Male; Microchemistry; Succinates | 1967 |
A case of hyperlysinemia: biochemical and clinical observations.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Autoanalysis; Child, Preschool; Chromatography, Paper; Citrulline; Humans; Intellectual Disability; Lysine; Male; Ornithine | 1967 |
Citrullinemia with defective urea production.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Diet Therapy; Female; Humans; Infant; Infant, Newborn; Intellectual Disability; Ligases; Liver; Seizures; Urea | 1967 |
Therapy of urea cycle enzymopathies: three case studies.
Topics: Ammonia; Arginine; Argininosuccinic Acid; Argininosuccinic Aciduria; Child, Preschool; Citrulline; Coma; Female; Humans; Infant; Infant, Newborn; Intellectual Disability; Lyases; Male; Ornithine Carbamoyltransferase Deficiency Disease; Urea | 1981 |
Long-term survival of patients with argininosuccinate synthetase deficiency.
Topics: Adolescent; Age of Onset; Amino Acids; Anthropometry; Argininosuccinate Synthase; Child; Child, Preschool; Citrulline; Clinical Protocols; Follow-Up Studies; Humans; Infant; Infant, Newborn; Intellectual Disability; Nutritional Status; Survival Rate | 1995 |
Liver transplantation for the treatment of urea cycle disorders.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Canada; Carbamoyl-Phosphate Synthase (Ammonia); Child; Citrulline; Communication Disorders; Female; Graft Rejection; Humans; Intellectual Disability; Liver Transplantation; Male; Microcephaly; Ornithine Carbamoyltransferase Deficiency Disease; Treatment Outcome; United States; Urea | 1998 |
Periodic hyperammonemia, hyperlysinemia, and homocitrullinuria associated with decreased argininosuccinate synthetase and arginase activities.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Arginase; Arginine; Argininosuccinate Synthase; Citrulline; Humans; Hyperargininemia; Intellectual Disability; Ligases; Liver; Lysine; Male | 1977 |
Clinical and biochemical studies on periodic hyperammonemia with hyperlysinemia and homocitrullinuria.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Anorexia; Arginase; Arginine; Citrulline; Erythrocytes; Growth Disorders; Humans; Intellectual Disability; Lysine; Male | 1976 |
[Hepato-cerebral diseases caused by abnormal amino acid metabolism ---clinical observation in 3 cases of citrullinemia].
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Citrulline; Electroencephalography; Female; Humans; Intellectual Disability; Liver Diseases | 1976 |
Biochemistry of mental retardation.
Topics: Aged; Citrulline; Female; Glycine; Histidine; Humans; Infant; Infant, Newborn; Intellectual Disability; Metabolism, Inborn Errors; Phenylketonurias | 1975 |
Haloperidol-induced hyperammonaemia in a child with citrullinaemia.
Topics: Ammonia; Attention Deficit Disorder with Hyperactivity; Child, Preschool; Citrulline; Haloperidol; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors | 1990 |
Possible pathogenetic mechanism in hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome.
Topics: Ammonia; Citrulline; Growth Disorders; Humans; Intellectual Disability; Liver; Lymphocytes; Mitochondria; Ornithine; Syndrome | 1987 |
The diagnosis of ornithine transcarbamylase deficiency.
Topics: Animals; Carbamyl Phosphate; Citrulline; Coma; Female; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Metabolism, Inborn Errors; Mitochondria; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid | 1985 |
[Use of a preparation with a base of L-citrulline and L-acetylaspartic acid in minors with "mental fatigue" and slight "mental retardation"].
Topics: Adolescent; Aspartic Acid; Child; Citrulline; Female; Humans; Intellectual Disability; Male; Mental Fatigue | 1966 |
Argininosuccinicaciduria: clinical, metabolic and dietary study.
Topics: Affective Symptoms; Amino Acid Metabolism, Inborn Errors; Ammonia; Arginase; Arginine; Ataxia; Child; Citrulline; Dietary Proteins; Electroencephalography; Epilepsy; Female; Humans; Intellectual Disability; Intelligence Tests; Male; Ornithine; Phenobarbital; Seizures; Succinates; Tremor | 1974 |
[Argininosuccinic aciduria with and without hyperammoniemia. Study of 2 cases].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Child; Child Behavior Disorders; Child, Preschool; Chromosome Aberrations; Citrulline; Dietary Proteins; Electrocardiography; Electroencephalography; Hepatomegaly; Humans; Intellectual Disability; Male; Movement Disorders; Seizures; Speech Disorders | 1973 |
Ornithinemia, hyperammonemia, and homocitrullinuria. A disease associated with mental retardation and possibly caused by defective mitochondrial transport.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Dietary Proteins; Female; Humans; Intellectual Disability; Lysine; Mitochondria; Ornithine; Ornithine Carbamoyltransferase; Proline; Transaminases | 1974 |
Citrullinemia: a new case, with implications concerning adaptation to defective urea synthesis.
Topics: Adult; Amino Acids; Ammonia; Citrulline; Dietary Proteins; Fibroblasts; Humans; Intellectual Disability; Ligases; Lysine; Male; Metabolism, Inborn Errors; Urea | 1972 |
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 |
Ultraviolet-absorbing components of urine from mentally retarded children. 3.
Topics: Adolescent; Adult; Ammonia; Autistic Disorder; Central Nervous System Diseases; Child; Child, Preschool; Chromatography, Ion Exchange; Chromatography, Paper; Citrulline; Creatinine; Dialysis; Humans; Hypnotics and Sedatives; Intellectual Disability; Male; Nephrectomy; Orotic Acid; RNA, Messenger; Sleep; Tranquilizing Agents; Ultraviolet Rays | 1970 |
Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Ataxia; Child, Preschool; Citrulline; Diet Therapy; Humans; Intellectual Disability; Lysine; Male; Myoclonus; Ornithine; Ornithine Carbamoyltransferase; Seizures | 1969 |
Argininosuccinic aciduria: clinical, biochemical, anatomical and neuropathological observations.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Arginine; Aspartic Acid; Brain; Cerebellum; Citrulline; Female; Humans; Infant; Intellectual Disability; Liver; Lyases; Myelin Sheath; Neuroglia; Succinates | 1969 |