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hydroxyproline and Phenylketonurias

hydroxyproline has been researched along with Phenylketonurias in 5 studies

Hydroxyproline: A hydroxylated form of the imino acid proline. A deficiency in ASCORBIC ACID can result in impaired hydroxyproline formation.
hydroxyproline : A proline derivative that is proline substituted by at least one hydroxy group.

Phenylketonurias: A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952).

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19905 (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
EFRON, ML2
YOUNG, D1
MOSER, HW1
MACCREADY, RA1
Goncerzewicz, M1
Socha, J1
Cichy, W1
Nagadowska, J1
Ampola, MG1
Menne, F1
Berio, A1
Di Stefano, A1
Bellati, R1
Viglione, M1

Reviews

2 reviews available for hydroxyproline and Phenylketonurias

ArticleYear
The aminoacidurias.
    Pediatric clinics of North America, 1967, Volume: 14, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; H

1967
[Feeble mindedness caused by genetic disorders of amino acid metabolism].
    Hippokrates, 1968, May-31, Volume: 39, Issue:10

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Glycine; Hartnup Disease; Histi

1968

Other Studies

3 other studies available for hydroxyproline and Phenylketonurias

ArticleYear
A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
    The New England journal of medicine, 1964, Jun-25, Volume: 270

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Chemical Analysis; Chromatography; Citrulli

1964
[Hydroxyproline indicators in the evaluation of nutritional status of children with various metabolic diseases].
    Pediatria polska, 1974, Volume: 49, Issue:2

    Topics: Child; Child Nutrition Disorders; Diabetes Mellitus, Type 1; Endocrine System Diseases; Female; Huma

1974
[The use of some recent methods for diagnosis of aminoacidopathy. Personal results].
    Minerva pediatrica, 1971, Sep-15, Volume: 23, Issue:37

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography; Electrophoresis; Fanconi Syndrome

1971