ammonium hydroxide has been researched along with Nervous System Diseases in 37 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Nervous System Diseases: Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Mitochondrial ornithine transporter deficiency has been called HHH syndrome, because this disorder is characterized by three biochemical abnormalities; hyperornithinemia, hyperammonemia, and homocitrullinuria, and presents with various neurological symptoms; mental retardation, spastic paraparesis with pyramidal signs, cerebellar ataxia and episodic disturbance of consciousness or coma due to hyperammonemia." | 8.81 | [Molecular genetic studies of mitochondrial ornithine transporter deficiency (HHH syndrome)]. ( Kanazawa, N; Miyamoto, T; Tsujino, S, 2001) |
| "Mitochondrial ornithine transporter deficiency has been called HHH syndrome, because this disorder is characterized by three biochemical abnormalities; hyperornithinemia, hyperammonemia, and homocitrullinuria, and presents with various neurological symptoms; mental retardation, spastic paraparesis with pyramidal signs, cerebellar ataxia and episodic disturbance of consciousness or coma due to hyperammonemia." | 4.81 | [Molecular genetic studies of mitochondrial ornithine transporter deficiency (HHH syndrome)]. ( Kanazawa, N; Miyamoto, T; Tsujino, S, 2001) |
| "We studied 26 children with inborn errors of urea synthesis who survived neonatal hyperammonemic coma." | 3.67 | Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies. ( Batshaw, ML; Brusilow, SW; Mellits, ED; Msall, M; Suss, R, 1984) |
| "Patients with cirrhosis were found to be extremely sensitive to tranylcypromine, and the use of this drug for the treatment of depression in such patients is contraindicated." | 3.65 | Antidepressants and liver disease. ( Morgan, MH; Read, AE, 1972) |
| "L-histidine (HIS) is an essential amino acid with unique roles in proton buffering, metal ion chelation, scavenging of reactive oxygen and nitrogen species, erythropoiesis, and the histaminergic system." | 2.66 | Histidine in Health and Disease: Metabolism, Physiological Importance, and Use as a Supplement. ( Holeček, M, 2020) |
| "Many neurologic disorders are related to congenital or acquired hyperammonemia (HA)." | 2.40 | Roles of neuroactive amino acids in ammonia neurotoxicity. ( Albrecht, J, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 24 (64.86) | 18.7374 |
| 1990's | 5 (13.51) | 18.2507 |
| 2000's | 5 (13.51) | 29.6817 |
| 2010's | 2 (5.41) | 24.3611 |
| 2020's | 1 (2.70) | 2.80 |
| Authors | Studies |
|---|---|
| Holeček, M | 1 |
| Mondal, P | 1 |
| Trigun, SK | 1 |
| Jayakumar, AR | 1 |
| Norenberg, MD | 1 |
| HARRIS, MM | 1 |
| ROTH, RT | 1 |
| HARRIS, RS | 1 |
| AIMARD, G | 1 |
| MAILLET, P | 1 |
| VILLAROS, J | 1 |
| DUFFRENE, D | 1 |
| FRANCOIS, B | 1 |
| Ortiz, M | 1 |
| Córdoba, J | 1 |
| Alonso, J | 1 |
| Rovira, A | 1 |
| Quiroga, S | 1 |
| Jacas, C | 1 |
| Esteban, R | 1 |
| Guardia, J | 1 |
| Singh, RH | 1 |
| Gropman, AL | 1 |
| Summar, M | 1 |
| Leonard, JV | 2 |
| Stegink, LD | 1 |
| Nomura, Y | 1 |
| Segawa, M | 1 |
| Hasegawa, M | 1 |
| Msall, M | 1 |
| Batshaw, ML | 1 |
| Suss, R | 1 |
| Brusilow, SW | 1 |
| Mellits, ED | 1 |
| Zapadlo, M | 1 |
| Zeman, J | 1 |
| Dubská, Z | 1 |
| Kvícala, J | 1 |
| Prusiner, SB | 1 |
| Rothberg, AD | 1 |
| Thomson, PD | 1 |
| Andronikou, S | 1 |
| Cohen, DF | 1 |
| Tollefsen, SE | 1 |
| McCabe, ER | 1 |
| Goodman, SI | 1 |
| Walter, JH | 1 |
| Wraith, JE | 1 |
| Cleary, MA | 1 |
| Brazil, TJ | 1 |
| Naylor, JM | 1 |
| Janzen, ED | 1 |
| Albrecht, J | 1 |
| Matsumura, R | 1 |
| Tsujino, S | 1 |
| Miyamoto, T | 1 |
| Kanazawa, N | 1 |
| Lemay, JF | 1 |
| Lambert, MA | 1 |
| Mitchell, GA | 1 |
| Vanasse, M | 1 |
| Valle, D | 1 |
| Arbour, JF | 1 |
| Dubé, J | 1 |
| Flessas, J | 1 |
| Laberge, M | 1 |
| Lafleur, L | 1 |
| Matsuoka, M | 1 |
| Igisu, H | 1 |
| Kohriyama, K | 1 |
| Inoue, N | 1 |
| Drogari, E | 1 |
| Mounger, EJ | 1 |
| Branson, AD | 1 |
| Conn, HO | 1 |
| Losowsky, MS | 1 |
| Scott, BB | 1 |
| Williams, R | 1 |
| Close, JH | 1 |
| Morgan, MH | 1 |
| Read, AE | 1 |
| O'Reilly, S | 1 |
| Price, JB | 1 |
| Sawada, M | 1 |
| Voorhees, AB | 1 |
| Zeegen, R | 1 |
| Drinkwater, JE | 1 |
| Fenton, JC | 1 |
| Vince, A | 1 |
| Dawson, AM | 1 |
| Pirotte, J | 1 |
| Pericoli, F | 1 |
| Hopkins, IJ | 1 |
| Connelly, JF | 1 |
| Hocking, B | 1 |
| Maddison, TG | 1 |
| Ivanchev, V | 1 |
| Vesin, P | 1 |
| Roberti, A | 1 |
11 reviews available for ammonium hydroxide and Nervous System Diseases
| Article | Year |
|---|---|
Histidine in Health and Disease: Metabolism, Physiological Importance, and Use as a Supplement.
Topics: Amino Acids, Branched-Chain; Ammonia; Chelating Agents; Contraindications; Dermatitis, Atopic; Dieta | 2020 |
Glutamine Synthetase: Role in Neurological Disorders.
Topics: Ammonia; Astrocytes; Glutamate-Ammonia Ligase; Glutamic Acid; Glutamine; Humans; Nervous System Dise | 2016 |
Nutritional management of patients with urea cycle disorders.
Topics: Adolescent; Adult; Ammonia; Child; Child, Preschool; Diet Therapy; Enzymes; Female; Humans; Hyperamm | 2007 |
Neurological implications of urea cycle disorders.
Topics: Ammonia; Brain; Cognition; Enzymes; Female; Humans; Hyperammonemia; Magnetic Resonance Imaging; Male | 2007 |
Amino acids in pediatric parenteral nutrition. Solutions infused--lessons learned.
Topics: Acid-Base Imbalance; Amino Acids; Ammonia; Child; Dicarboxylic Acids; England; History, 20th Century | 1983 |
Disorders of glutamate metabolism and neurological dysfunction.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; gamma-Aminobutyric Acid; Glutamates; Glutami | 1981 |
Roles of neuroactive amino acids in ammonia neurotoxicity.
Topics: Ammonia; Animals; Humans; Nervous System Diseases; Neurotransmitter Agents | 1998 |
[Disorders of the urea cycle].
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Argininosuccinic Acid; Citrullinemia; Human | 2000 |
[Molecular genetic studies of mitochondrial ornithine transporter deficiency (HHH syndrome)].
Topics: Amino Acid Transport Systems, Basic; Ammonia; Animals; Base Sequence; Carrier Proteins; Citrulline; | 2001 |
Hepatic encephalopathy.
Topics: Acetazolamide; Ammonia; Constipation; Diet Therapy; Electroencephalography; Gastrointestinal Hemorrh | 1973 |
The use of amino acid precursors in nitrogen-accumulation diseases.
Topics: Amino Acids; Amino Acids, Essential; Ammonia; Animals; Blood Urea Nitrogen; Chemical Phenomena; Chem | 1974 |
2 trials available for ammonium hydroxide and Nervous System Diseases
| Article | Year |
|---|---|
Complications of portacaval anastomosis. By-products of a controlled investigation.
Topics: Ammonia; Clinical Trials as Topic; Connecticut; Diabetes Mellitus; Gastric Juice; Hemosiderin; Hemos | 1973 |
Some observations on the effects of treatment with lactulose on patients with chronic hepatic encephalopathy.
Topics: Adult; Aged; Ammonia; Brain Diseases; Disaccharides; Electroencephalography; Feces; Female; Hepatiti | 1970 |
24 other studies available for ammonium hydroxide and Nervous System Diseases
| Article | Year |
|---|---|
Pannexin1 as a novel cerebral target in pathogenesis of hepatic encephalopathy.
Topics: Ammonia; Brain; Connexins; Energy Metabolism; Glutamic Acid; Heart Arrest; Hepatic Encephalopathy; H | 2014 |
Studies regarding glutamine and ammonia in the cerebrospinal fluid of patients with nervous and mental diseases (with some observations on insulin hypoglycemic shock and oligophrenia phenylpyruvica).
Topics: Ammonia; Cerebrospinal Fluid; Glutamine; Humans; Hypoglycemic Agents; Insulin; Intellectual Disabili | 1945 |
[Ammonemia and neurological disorders during experimental protacaval encephalopathy].
Topics: Ammonia; Brain; Brain Diseases; Humans; Nervous System Diseases; Neurologic Manifestations; Portacav | 1961 |
Oral glutamine challenge and magnetic resonance spectroscopy in three patients with congenital portosystemic shunts.
Topics: Administration, Oral; Adult; Ammonia; Area Under Curve; Brain; Cardiovascular Abnormalities; Female; | 2004 |
Rett syndrome--clinical studies and pathophysiological consideration.
Topics: Ammonia; Atrophy; Autistic Disorder; Cerebral Cortex; Child; Child Development; Child, Preschool; El | 1984 |
Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria | 1984 |
[Transient hyperammonemia in a full-term newborn infant].
Topics: Ammonia; Female; Humans; Infant; Infant, Newborn; Nervous System Diseases | 1984 |
Transient neonatal hyperammonaemia. A case report.
Topics: Ammonia; Diagnosis, Differential; Exchange Transfusion, Whole Blood; Female; Humans; Infant, Newborn | 1982 |
Neonatal hyperammonemia.
Topics: Adult; Ammonia; Asphyxia Neonatorum; Female; Humans; Hyaline Membrane Disease; Infant, Newborn; Nerv | 1980 |
Absence of acidosis in the initial presentation of propionic acidaemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Ammonia; Benzoates; Benzoic Acid; Carnitine; Food Pr | 1995 |
Ammoniated forage toxicosis in nursing calves: a herd outbreak.
Topics: Ammonia; Animal Feed; Animals; Cattle; Cattle Diseases; Diagnosis, Differential; Disease Outbreaks; | 1994 |
Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Child, Preschool; Citrullin | 1992 |
Suppression of neurotoxicity of ammonia by L-carnitine.
Topics: Ammonia; Animals; Behavior, Animal; Brain Chemistry; Carnitine; Energy Metabolism; Male; Mice; Mice, | 1991 |
Late onset ornithine carbamoyl transferase deficiency in males.
Topics: Adolescent; Age Factors; Ammonia; Child; Child, Preschool; Genetic Linkage; Heterozygote; Humans; In | 1988 |
Ammonia encephalopathy secondary to ureterosigmoidostomy: a case report.
Topics: Adult; Ammonia; Colon, Sigmoid; Coma; Enema; Female; Humans; Intestinal Absorption; Mental Disorders | 1972 |
Hepatic encephalopathy.
Topics: Acetaminophen; Ammonia; Animals; Brain; Brain Edema; Diet Therapy; Dopamine; Female; Humans; Lactulo | 1973 |
Antidepressants and liver disease.
Topics: Amitriptyline; Ammonia; Ammonium Chloride; Depression; Electroencephalography; Humans; Liver Cirrhos | 1972 |
Neurologic disorders and liver disease.
Topics: Adipose Tissue; Ammonia; Brain Diseases; Citrulline; Fatty Liver; Galactosemias; Hepatic Encephalopa | 1971 |
Clinical significance of intraluminal pH in intestinal ammonia transport.
Topics: Ammonia; Animals; Biological Transport; Colon; Dogs; Humans; Hydrogen-Ion Concentration; Intestinal | 1970 |
[Physiopathologic bases of treatment of portacaval encephalopathy].
Topics: Ammonia; Brain; Brain Diseases; Hepatic Encephalopathy; Humans; Liver Circulation; Liver Cirrhosis; | 1971 |
[Hepatic encephalopathy and its therapy with lactulose].
Topics: Ammonia; Disaccharides; Electroencephalography; Encephalitis; Humans; Hydrogen-Ion Concentration; Li | 1971 |
Neurological abnormalities in primary hyperammonaemia.
Topics: Ammonia; Diet Therapy; Dietary Proteins; Female; Humans; Infant; Intellectual Disability; Lysine; Me | 1968 |
[On changes in certain indices of autonomic reactivity in tobacco fermentation room workers].
Topics: Adult; Air Pollution; Ammonia; Autonomic Nervous System; Carbon Dioxide; Humans; Methanol; Middle Ag | 1968 |
[Treatment of porto-caval encephalopathy].
Topics: Ammonia; Brain Diseases; Humans; Liver Diseases; Nervous System Diseases | 1968 |