histidine has been researched along with Cystinuria in 21 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 21 (100.00) | 18.7374 |
1990's | 0 (0.00) | 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 |
---|---|
EFRON, ML | 1 |
GEROK, W; PABST, K | 1 |
DOWNING, S; ROSENBERG, LE | 1 |
Blackburn, P; Brown, A; Peterson, CM; Pospischil, MA; Rodman, JS; Williams, JJ | 1 |
Arakawa, T; Chikaoka, H; Katsushima, N; Kobayashi, M; Minagawa, A; Saito, TG; Shioji, R | 1 |
Brown, DA; Smith, A; Wilcken, B | 1 |
Bremer, HJ; Przyrembel, H | 1 |
Brown, DA; Connelly, J; Francis, I; Hill, G; Masters, P; McFarlane, J; Pitt, D; Raby, J; Tucker, RG; Wilcken, B | 1 |
berger, H; jarosch, E; Ludescher, E | 1 |
Bradley, DM | 1 |
Méhes, K; Mogyar, M; Németh, E | 1 |
Bundgaard, L; Winther, A | 1 |
Holmgren, G; Nordström, S; Thorburn, W | 1 |
Ampola, MG | 1 |
Levy, HL | 1 |
Tomaszewski, L | 1 |
Buravina, TA; Iur'eva, EA; Koroleva, IA; Lebedev, VP; Mukhina, IuG | 1 |
Brown, DA; Turner, B | 1 |
Holmgren, G; Jeppson, JO; Samuelson, G | 1 |
Antener, I | 1 |
5 review(s) available for histidine and Cystinuria
Article | Year |
---|---|
AMINOACIDURIA.
Topics: Amino Acid Metabolism, Inborn Errors; Biological Transport; Cystinuria; Histidine; Homocysteine; Humans; Hydroxyproline; Kidney; Methionine; Proline; Renal Aminoacidurias | 1965 |
[ON THE PATHOPHYSIOLOGY AND CLINICAL MANIFESTATIONS OF DISORDERS OF RENAL TUBULAR PARTIAL FUNCTION].
Topics: Acidosis; Acidosis, Renal Tubular; Amino Acids; Cystinuria; Diabetes Insipidus; Glycine; Glycosuria; Glycosuria, Renal; Histidine; Humans; Kidney Diseases; Kidney Tubules; Lipidoses; Renal Aminoacidurias; Tay-Sachs Disease; Urine | 1965 |
Phenylketonuria and other disorders of amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Child, Preschool; Counseling; Cystathionine; Cystinosis; Cystinuria; Diet Therapy; Dietary Proteins; Family; Female; Hartnup Disease; Histidine; Homocystinuria; Humans; Hyperglycemia; Infant; Infant, Newborn; Lysine; Maple Syrup Urine Disease; Ornithine; Phenylketonurias; Pregnancy; Proline; Tyrosine | 1973 |
Genetic screening.
Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Erythrocytes; Fanconi Syndrome; Galactosemias; Genetics, Population; Glucosephosphate Dehydrogenase; Glycine; Hartnup Disease; Heterozygote; Histidine; Homocystine; Humans; Lysine; Maple Syrup Urine Disease; Mass Screening; Methods; Ornithine; Phenylalanine; Phenylketonurias; Succinates; Tyrosine | 1973 |
[Primary and secondary hyperaminoaciduria in children (review of the literature)].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Biological Transport, Active; Cystinuria; Fanconi Syndrome; Glycine; Glycosuria, Renal; Hartnup Disease; Histidine; Humans; Infant, Newborn; Kidney Diseases; Kidney Tubules; Maple Syrup Urine Disease; Phenylketonurias; Proline; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Sodium | 1970 |
16 other study(ies) available for histidine and Cystinuria
Article | Year |
---|---|
TRANSPORT OF NEUTRAL AND DIBASIC AMINO ACIDS BY HUMAN LEUKOCYTES: ABSENCE OF DEFECT IN CYSTINURIA.
Topics: Alanine; Amides; Amino Acids; Amino Acids, Diamino; Aminoisobutyric Acids; Antimetabolites; Arginine; Biological Transport; Cyanides; Cystine; Cystinuria; Dinitrophenols; Fluorides; Genetics, Medical; Glycine; Histidine; Humans; Hydrogen-Ion Concentration; Leukocytes; Lysine; Methionine; Pharmacology | 1965 |
The effect of dietary protein on cystine excretion in patients with cystinuria.
Topics: Adolescent; Adult; Body Weight; Cystinuria; Dietary Proteins; Energy Intake; Female; Histidine; Humans; Kidney Calculi; Lysine; Male; Methylhistidines; Ornithine; Time Factors | 1984 |
Higher excretion of urinary bound amino acids in infants: probably related to protein-anabolic effect of growth hormone.
Topics: Aging; Alanine; Amino Acids; Arginine; Child; Child, Preschool; Cystine; Cystinuria; Glycine; Growth Hormone; Histidine; Humans; Infant; Isoleucine; Leucine; Lysine; Male; Methionine; Phenylalanine; Proteins; Valine | 1982 |
Urine screening for aminoacidopathies: is it beneficial? Results of a long-term follow-up of cases detected bny screening one millon babies.
Topics: Amino Acid Metabolism, Inborn Errors; Australia; Cystinuria; Follow-Up Studies; Histidine; Humans; Infant; Mass Screening | 1980 |
[Hereditary metabolic disorders with significance for adult age. Homocystinuria, histidinemia, cystinuria, vitamin-D-resistant rickets, alpha1-antitrypsin deficiency].
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 |
Genetic screening of the newborn in Australia. Results for 1978.
Topics: Australia; Blood Stains; Congenital Hypothyroidism; Cystinuria; Female; Fetal Blood; Genetic Testing; Histidine; Homocystinuria; Humans; Hypothyroidism; Infant, Newborn; Infant, Newborn, Diseases; Male; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias | 1979 |
[Disturbance of the Histidine Reabsorption of the Renal Tubes in Patient with Cystine Lysinuria in Conjunction with Severe Cerebral Damage (author's transl)].
Topics: Amino Acid Metabolism, Inborn Errors; Brain Damage, Chronic; Child; Cystinuria; Histidine; Humans; Intellectual Disability; Kidney Tubules; Levodopa; Lysine; Male; Parkinson Disease | 1975 |
Screening for inherited metabolic disease in Wales using urine-impregnated filter paper.
Topics: Alkaptonuria; Chromatography, Paper; Cystinuria; Diabetes Mellitus; Filtration; Glycosuria; Histidine; Homocystinuria; Humans; Infant, Newborn; Mass Screening; Metabolism, Inborn Errors; Paper; Phenylketonurias; Proteinuria; Wales | 1975 |
[Biochemical and genetic screening of newborn infants].
Topics: Blood Glucose; Chromatography, Thin Layer; Cystinuria; Histidine; Humans; Hungary; Infant, Newborn; Mass Screening; Phenylketonurias; Urine | 1975 |
Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study.
Topics: Amino Acid Metabolism, Inborn Errors; Argininosuccinic Acid; Australia; Cystinuria; Ethnicity; Europe; Galactosemias; Genetics, Population; Hartnup Disease; Histidine; Homocystinuria; Humans; Inbreeding; Infant, Newborn; Israel; Japan; Maple Syrup Urine Disease; Mass Screening; New Zealand; North America; Phenylketonurias; Tyrosine | 1975 |
Argininosuccinic aciduria in hereditary hair diseases.
Topics: Adolescent; Adult; Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Chromatography, Paper; Cystinuria; Female; Glutamates; Glutamine; Glycine; Hair; Histidine; Humans; Infant; Lysine; Male; Middle Aged; Serine; Skin Diseases; Threonine; Tyrosine; Valine | 1968 |
Urinary metabolic studies in hereditary macular degeneration.
Topics: Albuminuria; Amino Acids; Carbohydrates; Cystinuria; Electrophoresis, Paper; Female; Glycosuria; Histidine; Humans; Keto Acids; Male; Pedigree; Phenylketonurias; Retinal Degeneration; Syndrome; Tyrosine | 1974 |
[The inborn errors of metabolism of amino acids].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chemical Phenomena; Chemistry; Cystinuria; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Sarcosine; Tyrosine; Valine | 1973 |
Amino acid excretion in infancy and early childhood. A survey of 200,000 infants.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography; Cystathionine; Cystinuria; Glycine; Histidine; Humans; Infant; Lysine; Mass Screening; Phenylketonurias; Proline | 1972 |
High-voltage electrophoresis in urinary amino acid screening.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ampicillin; Chromatography; Cystinuria; Electrophoresis; Glycine; Histidine; Homocystinuria; Humans; Hydrogen-Ion Concentration; Mass Screening; Methods; Phenylketonurias; Renal Aminoacidurias | 1970 |
[Biochemical studies on inherited disorders of amino acid metabolism in pediatrics].
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Chemistry, Clinical; Child; Child, Preschool; Chromatography, Paper; Cystine; Cystinosis; Cystinuria; Electrophoresis; Fanconi Syndrome; Feces; Histidine; Humans; Keto Acids; Lysine; Maple Syrup Urine Disease; Ornithine; Phenylketonurias | 1970 |