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histidine and Hypophosphatemia, Familial

histidine has been researched along with Hypophosphatemia, Familial in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19902 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Scriver, CR1
Bremer, HJ; Przyrembel, H1

Reviews

1 review(s) available for histidine and Hypophosphatemia, Familial

ArticleYear
Garrod's legacy to the nations of mice and men.
    Progress in clinical and biological research, 1981, Volume: 45

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Biological Transport; Cell Membrane; Disease Models, Animal; Histidine; Humans; Hypophosphatemia, Familial; Metabolism, Inborn Errors; Mice; Mice, Mutant Strains; Ornithine Carbamoyltransferase Deficiency Disease; Phosphates; Proline Oxidase

1981

Other Studies

1 other study(ies) available for histidine and Hypophosphatemia, Familial

ArticleYear
[Hereditary metabolic disorders with significance for adult age. Homocystinuria, histidinemia, cystinuria, vitamin-D-resistant rickets, alpha1-antitrypsin deficiency].
    Der Internist, 1976, Volume: 17, Issue:7

    Topics: Adult; Age Factors; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Child; Cystinuria; Diagnosis, Differential; Histidine; Homocystinuria; Humans; Hypophosphatemia, Familial; Liver Cirrhosis; Marfan Syndrome; Metabolism, Inborn Errors; Pulmonary Emphysema

1976