proline has been researched along with Alkaptonuria in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (60.00) | 18.7374 |
1990's | 2 (40.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Beltrán-Valero de Bernabé, D; Fernández-Cañón, JM; Fernández-Ruiz, E; Granadino, B; Peñalva, MA; Renedo, M; Rodríguez de Córdoba, S | 1 |
Cabrera, VM; González, AM; González, P; Hernández, M; Larruga, JM; Pinto, FM; Ramos, SM; Roces, A | 1 |
Greco, GM; Magli, A | 1 |
Kroll, S; Toussaint, W; Zebisch, P | 2 |
1 review(s) available for proline and Alkaptonuria
Article | Year |
---|---|
[Eye manifestations of amino acid disorders].
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 |
4 other study(ies) available for proline and Alkaptonuria
Article | Year |
---|---|
The molecular basis of alkaptonuria.
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.
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].
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].
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 |