phenylalanine and Hypopituitarism

phenylalanine has been researched along with Hypopituitarism in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Arnhold, IJ; Kopp, P; Latronico, AC; Marui, S; Mendonca, BB; Osorio, MG1
Christiansen, JS; Jørgensen, JO; Møller, N; Nair, KS; Nørrelund, H1

Reviews

1 review(s) available for phenylalanine and Hypopituitarism

ArticleYear
Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1.
    The Journal of clinical endocrinology and metabolism, 2000, Volume: 85, Issue:8

    Topics: Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Consanguinity; Conserved Sequence; Female; Homeodomain Proteins; Humans; Hypopituitarism; Infant; Male; Phenylalanine; Pituitary Gland; Pituitary Hormones; Point Mutation; Radiography; Serine

2000

Other Studies

1 other study(ies) available for phenylalanine and Hypopituitarism

ArticleYear
Continuation of growth hormone (GH) substitution during fasting in GH-deficient patients decreases urea excretion and conserves protein synthesis.
    The Journal of clinical endocrinology and metabolism, 2001, Volume: 86, Issue:7

    Topics: Adult; Amino Acids; Blood Glucose; Calorimetry, Indirect; Fasting; Fatty Acids, Nonesterified; Female; Glycerol; Human Growth Hormone; Humans; Hydrocortisone; Hypopituitarism; Insulin; Insulin-Like Growth Factor I; Kinetics; Lipid Peroxidation; Lipids; Male; Middle Aged; Oxidation-Reduction; Phenylalanine; Protein Biosynthesis; Triiodothyronine; Urea

2001