ammonium hydroxide has been researched along with Galactosemias in 12 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Galactosemias: A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Extracorporeal liver perfusion in hepatic coma, used to eliminate toxic metabolites causing hepatic encephalopathy, is limited by the antibody (Ab) and complement-mediated hyperacute rejection of discordant xenografts." | 1.30 | Application of immunoapheresis for delaying hyperacute rejection during isolated xenogeneic pig liver perfusion. ( Hammer, C; Hoebel, G; Mueller-Derlich, J; Pascher, A; Poehlein, C; Stangl, M; Thiery, J, 1997) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (66.67) | 18.7374 |
| 1990's | 4 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Mowat, AP | 1 |
| Henderson, JM | 1 |
| Warren, WD | 1 |
| Pascher, A | 1 |
| Poehlein, C | 1 |
| Stangl, M | 1 |
| Hoebel, G | 1 |
| Thiery, J | 1 |
| Mueller-Derlich, J | 1 |
| Hammer, C | 1 |
| Cheung, KL | 1 |
| Tang, NL | 1 |
| Hsiao, KJ | 1 |
| Law, LK | 1 |
| Wong, W | 1 |
| Ng, PC | 1 |
| Pang, CP | 1 |
| Applegarth, DA | 1 |
| Fok, TF | 1 |
| Hjelm, NM | 1 |
| Maisawa, S | 1 |
| Takasago, Y | 1 |
| Oyake, Y | 1 |
| Maeta, H | 1 |
| Fujiwara, T | 1 |
| Goodman, SI | 1 |
| Greene, CL | 1 |
| Kolodny, EH | 1 |
| Yatziv, S | 1 |
| Holtzman, NA | 1 |
| Merin, S | 1 |
| Crawford, JS | 1 |
| Roschlau, G | 1 |
| O'Reilly, S | 1 |
| D'iachkova, AIa | 1 |
| Lebedev, BV | 1 |
6 reviews available for ammonium hydroxide and Galactosemias
| Article | Year |
|---|---|
Hepatic Disorders.
Topics: Adolescent; Adult; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Ammonia; Ch | 1982 |
Selective variceal decompression: current status and recent advances.
Topics: Amino Acids; Ammonia; Angiography; Ascites; Brain Diseases; Esophageal and Gastric Varices; Galactos | 1984 |
Classical galactosaemia in Chinese: A case report and review of disease incidence.
Topics: Ammonia; Asian People; China; Female; Galactosemias; Humans; Incidence; Infant, Newborn; Japan; Male | 1999 |
Inborn errors as causes of acute disease in infancy.
Topics: Acidosis, Lactic; Acute Disease; Ammonia; Galactosemias; Humans; Hyperglycemia; Infant; Infant, Newb | 1991 |
Dietary treatment of inborn errors of metabolism.
Topics: Ammonia; Carbohydrate Metabolism, Inborn Errors; Diet Therapy; Female; Fructose; Galactosemias; Glyc | 1970 |
[Mental retardation and hereditary enzymopathy (review)].
Topics: Ammonia; Carboxy-Lyases; Child; Child, Preschool; Eye Diseases; Galactosemias; Growth Disorders; Har | 1971 |
6 other studies available for ammonium hydroxide and Galactosemias
| Article | Year |
|---|---|
Application of immunoapheresis for delaying hyperacute rejection during isolated xenogeneic pig liver perfusion.
Topics: Acute Disease; Ammonia; Animals; Antibodies, Heterophile; Blood Component Removal; Complement C3; Co | 1997 |
Patent ductus venosus with hypoplastic right hepatoportal system in a young child born with asymmetric intra-uterine growth retardation.
Topics: Abnormalities, Multiple; Ammonia; Angiography, Digital Subtraction; Child, Preschool; Fetal Growth R | 1992 |
Laboratory approaches for inherited neurometabolic diseases.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Galactosemias; Homocystinuria; Humans; Lactates; Lact | 1985 |
The etiology of congenital cataracts. A survey of 386 cases.
Topics: Ammonia; Birth Weight; Cataract; Central Nervous System Diseases; Congenital Abnormalities; Down Syn | 1971 |
[The histological findings of tubular insufficiency in galactosemia, hereditary fructose intolerance, and oculocerebro-renal syndrome (Lowe-syndrome) (author's transl].
Topics: Ammonia; Autopsy; Carbohydrate Metabolism, Inborn Errors; Female; Fructose; Galactosemias; Growth Di | 1973 |
Neurologic disorders and liver disease.
Topics: Adipose Tissue; Ammonia; Brain Diseases; Citrulline; Fatty Liver; Galactosemias; Hepatic Encephalopa | 1971 |