ornithine and Brain Disorders

ornithine has been researched along with Brain Disorders in 16 studies

Research

Studies (16)

Timeframe	Studies, this research(%)	All Research%
pre-1990	12 (75.00)	18.7374
1990's	2 (12.50)	18.2507
2000's	1 (6.25)	29.6817
2010's	1 (6.25)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Jamuar, SS; Lim, JS; Qadri, SK; Ting, TW	1
GABUZDA, GJ; HALL, PW; SCHWARTZ, R	1
Hutchinson, JH; Jolley, RL; Labby, DH	1
Daune-Anglard, G; Seiler, N	1
Boveé, WM; Chamuleau, RA; Karlsen, OT; Mass, MA; Vogels, BA	1
Hayakawa, C; Kanazawa, N; Miyamoto, T; Tsujino, S	1
Amacher, AL; Bolton, RJ; Gatfield, PD	1
Tremblay, GC	1
Thaler, MM	1
Boswell, M; Hoogenraad, NJ; Thaler, MM	1
Honkonen, K	1
Girard, PF; Kopp, N; Trillet, M	1
Mundinger, F; Ostertag, C; Potthoff, PC	1
Merveille, P; Molimard, R; Paris, J	1
Bickel, H; Feist, D; Kekomäki, M; Müller, H; Quadbeck, G	1

Reviews

2 review(s) available for ornithine and Brain Disorders

Article	Year
Milder Form of Urea Cycle Defect Revisited: Report and Review of Hyperornithinaemia-Hyperammonaemia-Homocitrullinuria (HHH) Syndrome Diagnosed in a Teenage Girl Presenting with Recurrent Encephalopathy. Annals of the Academy of Medicine, Singapore, 2016, Volume: 45, Issue:12 Topics: Amino Acid Transport Systems, Basic; Brain Diseases; Child; Diet, Protein-Restricted; DNA Mutational Analysis; Female; Humans; Hyperammonemia; Mitochondrial Membrane Transport Proteins; Ornithine; Recurrence; Severity of Illness Index; Urea Cycle Disorders, Inborn	2016
Endogenous ornithine in search for CNS functions and therapeutic applications. Metabolic brain disease, 1993, Volume: 8, Issue:3 Topics: Ammonia; Animals; Brain; Brain Diseases; gamma-Aminobutyric Acid; Humans; Ornithine; Ornithine-Oxo-Acid Transaminase; Polyamines	1993

Article

Year

Milder Form of Urea Cycle Defect Revisited: Report and Review of Hyperornithinaemia-Hyperammonaemia-Homocitrullinuria (HHH) Syndrome Diagnosed in a Teenage Girl Presenting with Recurrent Encephalopathy.

Annals of the Academy of Medicine, Singapore, 2016, Volume: 45, Issue:12

Topics: Amino Acid Transport Systems, Basic; Brain Diseases; Child; Diet, Protein-Restricted; DNA Mutational Analysis; Female; Humans; Hyperammonemia; Mitochondrial Membrane Transport Proteins; Ornithine; Recurrence; Severity of Illness Index; Urea Cycle Disorders, Inborn

2016

Endogenous ornithine in search for CNS functions and therapeutic applications.

Metabolic brain disease, 1993, Volume: 8, Issue:3

Topics: Ammonia; Animals; Brain; Brain Diseases; gamma-Aminobutyric Acid; Humans; Ornithine; Ornithine-Oxo-Acid Transaminase; Polyamines

1993

Trials

1 trial(s) available for ornithine and Brain Disorders

Article	Year
[Haemostatic effect of ornithine-8-vasopressin (POR 8) in neurosurgical operations (author's transl)]. Der Anaesthesist, 1974, Volume: 23, Issue:7 Topics: Adult; Brain Diseases; Cerebrovascular Circulation; Drug Combinations; Electrocardiography; Epinephrine; Female; Hemostasis; Hemostatics; Humans; Male; Middle Aged; Ornithine; Tyrosine; Vasoconstrictor Agents; Vasopressins	1974

Other Studies

13 other study(ies) available for ornithine and Brain Disorders

Article	Year
METABOLISM OF ORNITHINE AND OTHER AMINO ACIDS IN THE CEREBRO-OCULO-RENAL SYNDROME. The American journal of medicine, 1964, Volume: 36 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
STUDIES OF RAT LIVER AND KIDNEY ENZYMES. I. RESPONSE TO MASSIVE INTRAGASTRIC DOSES OF CHRONICALLY ADMINISTERED NITROGENOUS SUBSTANCES. The American journal of clinical nutrition, 1964, Volume: 14 Topics: Alanine; Amino Acids; Ammonia; Arginine; Brain Diseases; Enzymes; Glutamates; Glutamine; Injections; Kidney; Liver; Liver Diseases; Nitrogen; Ornithine; Rats; Research; Stomach; Transaminases; Urea	1964
L-ornithine vs. L-ornithine-L-aspartate as a treatment for hyperammonemia-induced encephalopathy in rats. Journal of hepatology, 1997, Volume: 26, Issue:1 Topics: Ammonia; Analysis of Variance; Animals; Brain; Brain Diseases; Dipeptides; Drug Therapy, Combination; Magnetic Resonance Spectroscopy; Male; Microdialysis; Nitrogen; Ornithine; Portacaval Shunt, Surgical; Protons; Rats; Rats, Wistar; Synaptic Transmission	1997
A novel mutation, P126R, in a Japanese patient with HHH syndrome. Pediatric neurology, 2002, Volume: 26, Issue:1 Topics: Adolescent; Ammonia; Base Sequence; Brain Diseases; Carrier Proteins; Cysts; DNA Primers; Exons; Gene Expression; Humans; Magnetic Resonance Imaging; Male; Metabolism, Inborn Errors; Methionine; Mitochondrial Diseases; Molecular Sequence Data; Ornithine; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Septum Pellucidum; Syndrome; Tomography, X-Ray Computed	2002
Hyperammonemia (ornithinemia) presenting as a unilateral cerebral mass lesion. Surgical neurology, 1976, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Astrocytes; Brain Diseases; Brain Neoplasms; Carbamoyl-Phosphate Synthase (Ammonia); Cerebral Cortex; Child, Preschool; Diagnosis, Differential; Functional Laterality; Glioma; Humans; Male; Ornithine; Syndrome	1976
Letter: Ornithine or citrulline therapy in treatment of Reye's syndrome. The New England journal of medicine, 1975, Jan-16, Volume: 292, Issue:3 Topics: Animals; Brain Diseases; Citrulline; Humans; In Vitro Techniques; Ornithine; Rats; Reye Syndrome	1975
Pathogenesis of Reye's syndrome: A working hypothesis. Pediatrics, 1975, Volume: 56, Issue:6 Topics: Ammonia; Arginine; Brain Diseases; Child; Humans; Ornithine; Reye Syndrome	1975
Editorial: Encephalopathy and fatty degeneration of viscera. Lancet (London, England), 1974, Aug-24, Volume: 2, Issue:7878 Topics: Age Factors; Ammonia; Arginine; Brain Diseases; Chickenpox; Child; Fatty Liver; Humans; Influenza, Human; Ornithine; Orthomyxoviridae; Reye Syndrome; Transaminases; Urea	1974
Reye's syndrome due to a novel protein-tolerant variant of ornithine-transcarbamylase deficiency. Lancet (London, England), 1974, Aug-24, Volume: 2, Issue:7878 Topics: Ammonia; Brain Diseases; Child; Fatty Liver; Female; Hepatic Encephalopathy; Humans; Kinetics; Liver; Metabolism, Inborn Errors; Ornithine; Ornithine Carbamoyltransferase; Prothrombin Time; Reye Syndrome; Urea	1974
[Correction by L-dopa of neurologic manifestations of a chronic portocaval encephalopathy]. Revue neurologique, 1972, Volume: 127, Issue:5 Topics: Alcoholism; Ammonia; Brain Diseases; Dihydroxyphenylalanine; Electroencephalography; Humans; Ketoglutaric Acids; Lactulose; Liver Cirrhosis; Male; Middle Aged; Neurologic Manifestations; Ornithine; Prednisone; Silicosis; Tremor	1972
[Clinical use of ornithine-8-vasopressin in addition to a local anesthetic in neurosurgery]. Schweizer Archiv fur Neurologie, Neurochirurgie und Psychiatrie = Archives suisses de neurologie, neurochirurgie et de psychiatrie, 1971, Volume: 108, Issue:2 Topics: Adult; Analgesia; Anesthesia, General; Anesthetics, Local; Blood Pressure; Brain Diseases; Brain Neoplasms; Craniotomy; Epinephrine; Female; Hemorrhage; Hemostasis; Humans; Male; Middle Aged; Ornithine; Pallor; Parkinson Disease; Postoperative Complications; Pulse; Stereotaxic Techniques; Trephining; Vasoconstrictor Agents; Vasopressins; Wound Healing	1971
[1 (+) ornithine alpha ketoglutarate in hepatic encephalopathy]. La Presse medicale, 1970, Jun-20, Volume: 78, Issue:30 Topics: Brain Diseases; Electroencephalography; Hepatic Encephalopathy; Hepatitis; Humans; Ketoglutaric Acids; Liver Cirrhosis; Liver Diseases; Liver Neoplasms; Ornithine	1970
Ornithinaemia. Another disorder of aminoacid metabolism associated with brain damage. German medical monthly, 1969, Volume: 14, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Brain Diseases; Child; Child, Preschool; Female; Humans; Male; Ornithine; Transaminases	1969