Page last updated: 2024-08-17

histidine and Cystinuria

histidine has been researched along with Cystinuria in 21 studies

Research

Studies (21)

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

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

Reviews

5 review(s) available for histidine and Cystinuria

Article	Year
AMINOACIDURIA. The New England journal of medicine, 1965, May-27, Volume: 272 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]. Munchener medizinische Wochenschrift (1950), 1965, Jan-08, Volume: 107 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. Pediatric clinics of North America, 1973, Volume: 20, Issue:2 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. Advances in human genetics, 1973, Volume: 4 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)]. Voprosy okhrany materinstva i detstva, 1970, Volume: 15, Issue:11 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

Other Studies

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. The Journal of clinical investigation, 1965, Volume: 44 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. Clinical nephrology, 1984, Volume: 22, Issue:6 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. The Tohoku journal of experimental medicine, 1982, Volume: 137, Issue:1 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. The Journal of pediatrics, 1980, Volume: 97, Issue:3 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]. 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
Genetic screening of the newborn in Australia. Results for 1978. The Medical journal of Australia, 1979, Sep-08, Volume: 2, Issue:5 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)]. Padiatrie und Padologie, 1975, Volume: 10, Issue:1 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. Archives of disease in childhood, 1975, Volume: 50, Issue:4 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]. Orvosi hetilap, 1975, Aug-24, Volume: 116, Issue:34 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. Humangenetik, 1975, Dec-23, Volume: 30, Issue:4 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. Acta dermato-venereologica, 1968, Volume: 48, Issue:6 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. Acta ophthalmologica, 1974, Volume: 52, Issue:2 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]. Postepy biochemii, 1973, Volume: 19, Issue:1 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. The Medical journal of Australia, 1972, Jan-08, Volume: 1, Issue:2 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. Scandinavian journal of clinical and laboratory investigation, 1970, Volume: 26, Issue:4 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]. Zeitschrift fur klinische Chemie und klinische Biochemie, 1970, Sep-08, Volume: 7, Issue:5 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