ornithine has been researched along with Intellectual Disability in 27 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 23 (85.19) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 4 (14.81) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Angle, B; Araújo, HC; Barshop, B; Coskun, T; Diogo, L; Geraghty, M; Grolik, C; Haliloglu, G; Konstantopoulou, V; Korenke, GC; Leuzzi, V; Levtova, A; Longo, N; Mackenzie, J; Maranda, B; Marquart, I; Mercimek-Mahmutoglu, S; Mhanni, AA; Mitchell, G; Morris, A; Newlove, T; Nyhan, W; Renaud, D; Scaglia, F; Schlune, A; Schulze, A; Stockler-Ipsiroglu, S; Valayannopoulos, V; van Karnebeek, C; van Spronsen, FJ; Verbruggen, KT; Yuskiv, N | 1 |
| Braissant, O | 1 |
| Nguyen, T; Pitt, JJ; Tzanakos, N | 1 |
| Cheillan, D; Dessein, AF; Dobbelaere, D; Fontaine, M; Joncquel-Chevalier Curt, M; Mention-Mulliez, K; Porchet, N; Soto-Ares, G; Vamecq, J; Voicu, PM | 1 |
| GABUZDA, GJ; HALL, PW; SCHWARTZ, R | 1 |
| Courtecuisse, V; Dommergues, JP; Girard, F; Limal, JM | 1 |
| Armstrong, MD; Robinow, M | 1 |
| Prisco, F; Santinelli, R; Stoppoloni, G; Tolone, C | 1 |
| Jarosch, E; Plöchl, E | 1 |
| Colombo, JP; Lavinha, F; Lowenthal, A; Terheggen, HG | 1 |
| Eskelin, LE; Perheentupa, J; Rapola, J; Simell, O; Visakorpi, JK | 1 |
| Beaudry, MA; Collu, R; Dallairf, L; Ducharme, JR; Leboeuf, G; Letarte, J; Melancon, SB | 1 |
| Gordon, BA; Haust, MD | 1 |
| Alme, A; Broch, H; Gjessing, LR; Lie, SO; Lunde, H; Undrum, T | 1 |
| Fluharty, AL; Kihara, H; Porter, MT; Valente, M | 1 |
| Bicknell, J; Cavanagh, NP; Howard, F | 1 |
| Brenton, DP; Cusworth, DC; Hartley, S; Kuzemko, JA; Lumley, S | 1 |
| Oldendorf, WH | 1 |
| Iivanainen, M; Palo, J; Savolainen, H | 1 |
| Fell, V; Pollitt, RJ; Sampson, GA; Wright, T | 1 |
| Szliwowski, HB; Thiriar, MJ; Vis, HL | 1 |
| Miura, R; Oyanagi, K; Yamanouchi, T | 1 |
| Kajii, T; Matsuda, I; Sugai, M | 1 |
| Bickel, H; Feist, D; Müller, H; Quadbeck, G | 1 |
| Greer, M; Sprinkle, T; Williams, CM | 1 |
| Efron, ML; Moser, HW; Shih, VE | 1 |
| Efron, ML; Holmes, LB; McGowan, BL | 1 |
1 review(s) available for ornithine and Intellectual Disability
| Article | Year |
|---|---|
Creatine biosynthesis and transport in health and disease.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Amino Acid Transport Systems, Basic; AMP-Activated Protein Kinases; Animals; Biological Transport, Active; Brain Diseases, Metabolic, Inborn; Creatine; Developmental Disabilities; Energy Metabolism; Guanidinoacetate N-Methyltransferase; Gyrate Atrophy; Humans; Hyperammonemia; Intellectual Disability; Language Development Disorders; Mental Retardation, X-Linked; Methylation; Mitochondrial Membrane Transport Proteins; Movement Disorders; Mutation; Nerve Tissue Proteins; Ornithine; Plasma Membrane Neurotransmitter Transport Proteins; Prenatal Diagnosis; S-Adenosylmethionine; Speech Disorders; Urea Cycle Disorders, Inborn | 2015 |
26 other study(ies) available for ornithine and Intellectual Disability
| Article | Year |
|---|---|
Guanidinoacetate methyltransferase (GAMT) deficiency: outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoring.
Topics: Adolescent; Adult; Arginine; Brain; Child; Child, Preschool; Combined Modality Therapy; Creatine; Female; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Infant; Infant, Newborn; Intellectual Disability; Language Development Disorders; Male; Middle Aged; Movement Disorders; Ornithine; Practice Guidelines as Topic; Sodium Benzoate; Treatment Outcome; Young Adult | 2014 |
GAMT deficiency: 20 years of a treatable inborn error of metabolism.
Topics: Arginine; Creatine; Female; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Intellectual Disability; Language Development Disorders; Male; Movement Disorders; Ornithine; Sodium Benzoate | 2014 |
Newborn screening for guanidinoacetate methyl transferase deficiency.
Topics: Arginine; Creatine; Diet; Female; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Intellectual Disability; Language Development Disorders; Male; Metabolism, Inborn Errors; Movement Disorders; Ornithine; Sodium Benzoate | 2014 |
METABOLISM OF ORNITHINE AND OTHER AMINO ACIDS IN THE CEREBRO-OCULO-RENAL SYNDROME.
Topics: Amino Acids; Blood Chemical Analysis; Brain Diseases; Cataract; Genetics, Medical; Glaucoma; Humans; Intellectual Disability; Kidney Diseases; Oculocerebrorenal Syndrome; Ophthalmology; Ornithine; Proteins; Reflex; Reflex, Abnormal; Urine | 1964 |
[Growth in height, bone and endocrine abnormalities in hypoplasia of the intrahepatic bile ducts. Eleven cases].
Topics: Abnormalities, Multiple; Adolescent; Adult; Arginine; Bile Ducts, Intrahepatic; Body Height; Bone and Bones; Cardiovascular Abnormalities; Child; Child, Preschool; Cholestasis; Endocrine System; Female; Fibrosis; Follow-Up Studies; Growth Disorders; Growth Hormone; Humans; Intellectual Disability; Male; Ornithine; Osteoporosis; Syndrome; Testis | 1976 |
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 |
Hyperornithinemia and gyrate atrophy of choroid and retina. Report of a case.
Topics: Atrophy; Child, Preschool; Dietary Proteins; Female; Humans; Intellectual Disability; Language Development; Ornithine; Ornithine-Oxo-Acid Transaminase; Retinal Diseases; Speech Disorders; Syndrome; Transaminases; Uveal Diseases | 1978 |
[Congenital hyperlysin-arginin-ornithinuria in a mentally retarded child (author's transl)].
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Biological Transport, Active; Child, Preschool; Humans; Intellectual Disability; Kidney; Lysine; Male; Ornithine | 1977 |
Familial hyperargininaemia.
Topics: Amino Acids; Ammonia; Arginine; Athetosis; Child, Preschool; Chromatography; Cystinuria; Dietary Proteins; Erythrocytes; Female; Guanidines; Humans; Hyperargininemia; Infant; Infant, Newborn; Intellectual Disability; Metabolism, Inborn Errors; Muscle Spasticity; Ornithine; Umbilical Cord; Urea | 1975 |
Lysinuric protein intolerance.
Topics: Adolescent; Adult; Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Arginine; Birth Weight; Child; Child, Preschool; Dietary Proteins; Eye Diseases; Female; Humans; Infant; Intellectual Disability; Intestinal Absorption; Liver; Lysine; Male; Nitrogen; Ornithine; Proteins; Renal Aminoacidurias; Urea | 1975 |
[Chronic hyperammonemia with orotic aciduria: evidence of pyrimidine pathway stimulation (author's transl)].
Topics: Alanine; Amino Acids; Ammonia; Child, Preschool; Dietary Proteins; Erythrocytes; Growth Disorders; Humans; Intellectual Disability; Leukocytes; Ornithine; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Orotate Phosphoribosyltransferase; Orotic Acid; Orotidine-5'-Phosphate Decarboxylase; Purine-Pyrimidine Metabolism, Inborn Errors; Pyrimidines; Seizures; Syndrome; Urea | 1975 |
Possible pathogenetic mechanism in hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome.
Topics: Ammonia; Citrulline; Growth Disorders; Humans; Intellectual Disability; Liver; Lymphocytes; Mitochondria; Ornithine; Syndrome | 1987 |
[Shih syndrome. A biochemical deviation in ornithine metabolism leading to mental retardation].
Topics: Amino Acids; Dietary Proteins; Humans; Infant; Intellectual Disability; Male; Metabolism, Inborn Errors; Ornithine; Syndrome | 1985 |
Hyperdibasicaminoaciduria in a mentally retarded homozygote with a peculiar response to phenothiazines.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Antipsychotic Agents; Arginine; Chlorpromazine; Cystinuria; Female; Fluphenazine; Humans; Intellectual Disability; Intestinal Absorption; Kidney Tubules; Lysine; Movement Disorders; Ornithine; Pedigree; Renal Aminoacidurias; Thioridazine; Trihexyphenidyl | 1973 |
Cystinuria with mental retardation and paroxysmal dyskinesia in 2 brothers.
Topics: Arginine; Child; Cystinuria; Humans; Intellectual Disability; Lysine; Male; Movement Disorders; Ornithine | 1974 |
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 |
Saturation of blood brain barrier transport of amino acids in phenylketonuria.
Topics: Amino Acids; Animals; Arginine; Blood-Brain Barrier; Brain; Carbon Isotopes; Dihydroxyphenylalanine; Female; Histidine; Humans; Intellectual Disability; Isoleucine; Leucine; Lysine; Male; Methionine; Ornithine; Phenylalanine; Phenylketonurias; Rats; Threonine; Tryptophan; Tyrosine; Valine | 1973 |
Free amino acids and carbohydrates in the cerebrospinal fluid of 305 mentally retarded patients: a screening study.
Topics: Adolescent; Adult; Alanine; Amino Acids; Arginine; Carbohydrates; Child; Child, Preschool; Chromatography, Thin Layer; Cystine; Epilepsy; Female; Glutamates; Glutamine; Humans; Intellectual Disability; Intelligence Tests; Isoleucine; Leucine; Lysine; Male; Metabolism, Inborn Errors; Methionine; Middle Aged; Ornithine; Phenylalanine; Pneumoencephalography; Threonine; Valine | 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 |
[Combined cystinuria-lysinuria in 2 brothers with mental retardation and morphologic and neurologic anomalies].
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Child; Cystinuria; Female; Humans; Infant; Intellectual Disability; Lysine; Male; Middle Aged; Ornithine | 1968 |
Congenital lysinuria: a new inherited transport disorder of dibasic amino acids.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Arginine; Biological Transport; Child; Chromatography, Thin Layer; Consanguinity; Cystine; Cystinuria; Diarrhea; Female; Growth; Humans; Intellectual Disability; Lysine; Malabsorption Syndromes; Ornithine; Renal Aminoacidurias; Vomiting | 1970 |
Ornithine loading test in Lowe's syndrome.
Topics: Abnormalities, Multiple; Amino Acids; Ammonia; Chromosome Aberrations; Chromosome Disorders; Eye Diseases; Growth Disorders; Humans; Intellectual Disability; Kidney Diseases; Ornithine | 1970 |
[Ornithinemia, additional disorder of amino acid metabolism with brain damage].
Topics: Amino Acids; Brain Damage, Chronic; Child; Child, Preschool; Electroencephalography; Female; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Methods; Nitrogen; Ornithine; Transaminases | 1968 |
Detection of argininosuccinic aciduria by gas chromatography.
Topics: Arginine; Aspartic Acid; Ataxia; Chemical Precipitation; Chromatography, Gas; Epilepsy; Esters; Humans; Hydrogen-Ion Concentration; Intellectual Disability; Liver Diseases; Metabolism, Inborn Errors; Methods; Ornithine; Spectrum Analysis; Succinates | 1969 |
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 |
Lowe's syndrome: a search or the carrier state.
Topics: Acidosis, Renal Tubular; Adolescent; Adult; Amino Acids; Cataract; Child, Preschool; Cytogenetics; Eye Manifestations; Female; Glaucoma; Humans; Infant; Intellectual Disability; Lens, Crystalline; Male; Middle Aged; Ornithine; Pedigree | 1969 |