proline and Alkaptonuria

proline has been researched along with Alkaptonuria in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19903 (60.00)18.7374
1990's2 (40.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Beltrán-Valero de Bernabé, D; Fernández-Cañón, JM; Fernández-Ruiz, E; Granadino, B; Peñalva, MA; Renedo, M; Rodríguez de Córdoba, S1
Cabrera, VM; González, AM; González, P; Hernández, M; Larruga, JM; Pinto, FM; Ramos, SM; Roces, A1
Greco, GM; Magli, A1
Kroll, S; Toussaint, W; Zebisch, P2

Reviews

1 review(s) available for proline and Alkaptonuria

ArticleYear
[Eye manifestations of amino acid disorders].
    Minerva pediatrica, 1978, May-31, Volume: 30, Issue:10

    Topics: Alanine; Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Child; Cystinosis; Cystinuria; Eye Diseases; Eye Manifestations; Glycine; Hartnup Disease; Hepatolenticular Degeneration; Homocystinuria; Humans; Lysine; Oculocerebrorenal Syndrome; Oxidoreductases; Phenylketonurias; Proline; Pyruvates

1978

Other Studies

4 other study(ies) available for proline and Alkaptonuria

ArticleYear
The molecular basis of alkaptonuria.
    Nature genetics, 1996, Volume: 14, Issue:1

    Topics: Alkaptonuria; Amino Acid Sequence; Base Sequence; Chromosome Mapping; Chromosomes, Human, Pair 3; Cloning, Molecular; Dioxygenases; DNA, Complementary; Female; Homogentisate 1,2-Dioxygenase; Humans; Male; Molecular Sequence Data; Oxygenases; Point Mutation; Proline; Serine; Tissue Distribution

1996
Molecular diagnosis of alkaptonuria mutation by analysis of homogentisate 1,2 dioxygenase mRNA from urine and blood.
    American journal of medical genetics, 1998, Jun-30, Volume: 78, Issue:2

    Topics: Alkaptonuria; Amino Acid Substitution; Dioxygenases; Female; Homogentisate 1,2-Dioxygenase; Humans; Male; Oxygenases; Pedigree; Point Mutation; Proline; RNA, Messenger; Serine

1998
[Hereditary amino acid metabolism disorders. Indications for early diagnosis].
    Fortschritte der Medizin, 1972, Apr-13, Volume: 90, Issue:11

    Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Cystathionine; Cystinosis; Diagnosis, Differential; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine

1972
[Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
    Fortschritte der Medizin, 1972, Apr-13, Volume: 90, Issue:11

    Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Clinical Laboratory Techniques; Cystathionine; Cystinosis; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine

1972