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ammonium hydroxide and Lipid Metabolism, Inborn Error

ammonium hydroxide has been researched along with Lipid Metabolism, Inborn Error in 7 studies

azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.

Research Excerpts

ExcerptRelevanceReference
"Today we know a great number of inborn errors of metabolism which can be treated by a special diet."1.27[Nutrition in congenital metabolic diseases]. ( Plöchl, E, 1984)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19905 (71.43)18.7374
1990's2 (28.57)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Plöchl, E1
Ogier de Baulny, H1
Slama, A1
Touati, G1
Turnbull, DM1
Pourfarzam, M1
Brivet, M1
Imamura, Y1
Saheki, T1
Arakawa, H1
Noda, T1
Koizumi, T1
Nikaido, H1
Hayakawa, J1
Kolodny, EH1
Yatziv, S1
Gardner, LI1
Pabico, RC1
Atancio, BC1
McKenna, BA1
Pamukcoglu, T1
Yodaiken, R1
Danis, MP1

Reviews

1 review available for ammonium hydroxide and Lipid Metabolism, Inborn Error

ArticleYear
Genetically expressed abnormalities in the fetus.
    Clinical obstetrics and gynecology, 1974, Volume: 17, Issue:3

    Topics: Adrenal Insufficiency; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Ammonia; Anemia, S

1974

Other Studies

6 other studies available for ammonium hydroxide and Lipid Metabolism, Inborn Error

ArticleYear
[Nutrition in congenital metabolic diseases].
    Padiatrie und Padologie, 1984, Volume: 19, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Carbohydrate Metabolism, Inborn Errors;

1984
Neonatal hyperammonemia caused by a defect of carnitine-acylcarnitine translocase.
    The Journal of pediatrics, 1995, Volume: 127, Issue:5

    Topics: Ammonia; Carnitine Acyltransferases; Diagnosis, Differential; Diseases in Twins; Fatal Outcome; Fema

1995
Urea cycle disorder in C3H-H-2 degree mice with juvenile steatosis of viscera.
    FEBS letters, 1990, Jan-15, Volume: 260, Issue:1

    Topics: Ammonia; Animals; Fatty Liver; Gene Expression Regulation, Enzymologic; Homozygote; Lipid Metabolism

1990
Laboratory approaches for inherited neurometabolic diseases.
    Developmental medicine and child neurology, 1985, Volume: 27, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Galactosemias; Homocystinuria; Humans; Lactates; Lact

1985
Renal pathologic lesions and functional alterations in a man with Fabry's disease.
    The American journal of medicine, 1973, Volume: 55, Issue:3

    Topics: Ammonia; Epithelial Cells; Glomerular Filtration Rate; Glycolipids; Humans; Hydrogen-Ion Concentrati

1973
[Anatomo-clinical correlations in some metabolic and tumoral ocular diseases].
    Bulletin des societes d'ophtalmologie de France, 1973, Volume: 73, Issue:2

    Topics: Adult; Ammonia; Brain Neoplasms; Cataract; Child; Child, Preschool; Ciliary Body; Eye; Eye Diseases;

1973