histidine has been researched along with Classic Galactosemia in 30 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 30 (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 |
---|---|
COFFEY, VP | 1 |
Aoki, K; Arashima, S; Kawamura, M; Kitagawa, T; Oura, T; Sakai, K; Suwa, S; Tada, K; Takesada, M; Tateda, H | 1 |
Yasuda, N | 1 |
Alm, J; Larsson, A; Rosenqvist, U | 1 |
Mamunes, P | 2 |
Alm, J; Larsson, A | 1 |
Schmid-Rüter, E | 2 |
Krüger, M; Menne, F; Otte, HJ; Winterhoff, D | 1 |
Enzenauer, J; Matz, D; Menne, F | 1 |
Hill, GN; Pollard, AC; Robertson, EF | 1 |
Menne, F | 1 |
Davidow, B; Goldberg, D; Grossi, M; Grover, R; Shahidi, S; Wethers, D | 1 |
Bickel, H | 1 |
Aoki, K; Wada, Y | 1 |
Clayton, BE | 1 |
Levy, HL | 2 |
Thalhammer, O | 1 |
Bozkowa, K; Cabalska, MB | 1 |
Scheiber, V; Thalhammer, O | 1 |
Knoll, E; Scheibenreiter, S; Schmierer, G; Schön, R; Thalhammer, O | 1 |
Steuer, W | 1 |
Carson, NA; Martin, VA | 1 |
Biedl, E; Scheibenreiter, S; Thalhammer, O | 1 |
Giovannini, M | 1 |
Bauer, B | 1 |
3 review(s) available for histidine and Classic Galactosemia
Article | Year |
---|---|
Neonatal screening tests.
Topics: Adenosine Deaminase; Anemia, Sickle Cell; Biological Assay; Costs and Cost Analysis; Galactosemias; Histidine; Homocystinuria; Humans; Infant, Newborn; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Tyrosine; United States | 1980 |
Newborn screening for metabolic disorders.
Topics: Chromatography, Paper; Congenital Hypothyroidism; Cost-Benefit Analysis; Costs and Cost Analysis; Female; Fluorometry; Galactosemias; Histidine; Humans; Hypothyroidism; Infant, Newborn; Infant, Newborn, Diseases; Metabolism, Inborn Errors; Phenylketonurias; Pregnancy; Time Factors; United States; UTP-Hexose-1-Phosphate Uridylyltransferase | 1976 |
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 |
27 other study(ies) available for histidine and Classic Galactosemia
Article | Year |
---|---|
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Fructose; Galactosemias; Histidine; Homocysteine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Vitamin B 6 Deficiency | 1964 |
Follow-up study of a nation-wide neonatal metabolic screening program in Japan. A collaborative study group of neonatal screening for inborn errors of metabolism in Japan.
Topics: Biopterins; Female; Follow-Up Studies; Galactosemias; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Intelligence; Japan; Male; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias | 1984 |
Geographical variations in inborn errors of metabolism in Japan.
Topics: Amino Acid Metabolism, Inborn Errors; Galactosemias; Histidine; Humans; Japan; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Phenylketonurias | 1984 |
Health economic analysis of the Swedish neonatal metabolic screening programme. A method of optimizing routines.
Topics: Amino Acid Metabolism, Inborn Errors; Cost-Benefit Analysis; Galactosemias; Histidine; Homocystinuria; Humans; Infant, Newborn; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Sweden; Tyrosine | 1982 |
Evaluation of a nation-wide neonatal metabolic screening programme in Sweden 1965-1979.
Topics: Evaluation Studies as Topic; Galactosemias; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Sweden; Tyrosine | 1981 |
[Early diagnosis of hereditary metabolic diseases in the newborn by means of microbiological Guthrie tests].
Topics: Bacillus subtilis; Galactosemias; Germany, West; Histidine; Homocystinuria; Humans; Infant, Newborn; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Microbiological Techniques; Phenylketonurias | 1978 |
[Screening of the Westphalia-Lippe newborns of 1977 for phenylketonuria, histidinemia, homocystinuria and maple syrup disease. Furthermore a pilot study of galactosemia and galactokinase deficiency disease].
Topics: Galactokinase; Galactosemias; Germany, West; Histidine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Maple Syrup Urine Disease; Mass Screening; Metabolic Diseases; Phenylketonurias | 1979 |
[Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2].
Topics: Acute Disease; Diagnosis, Differential; Galactose; Galactosemias; Germany, West; Histidine; Homocystine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Methionine; Phosphotransferases | 1976 |
Evaluation of a state-wide neonatal screening programme.
Topics: alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Australia; Evaluation Studies as Topic; Follow-Up Studies; Galactosemias; Histidine; Humans; Hypothyroidism; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine | 1979 |
[Screening and therapy of 6 metabolic diseases of hereditary nature which are possible causes of mental retardation: screening of 1,900,000 newborn infants since the year 1965].
Topics: Galactosemias; Germany, West; Histidine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias | 1979 |
Evaluation of the expanded newborn screening program in New York City.
Topics: Adenosine Deaminase; Anemia, Sickle Cell; Costs and Cost Analysis; Counseling; Galactosemias; Hemoglobinopathies; Histidine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Legislation, Medical; Mass Screening; Metabolic Diseases; New York; New York City; Organization and Administration; Phenylketonurias | 1978 |
[Methods and results of screening newborn infants for aminoacidopathies].
Topics: Amino Acid Metabolism, Inborn Errors; Europe; Galactosemias; Germany, West; Histidine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Maple Syrup Urine Disease; Mass Screening; Phenylketonurias | 1976 |
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 |
Outcome of the patients detected by newborn screening in Japan.
Topics: Amino Acid Metabolism, Inborn Errors; Biopterins; Female; Follow-Up Studies; Galactosemias; Histidine; Humans; Infant, Newborn; Japan; Male; Mass Screening; Phenylalanine | 1988 |
Problems affecting the community. Population screening.
Topics: Cystic Fibrosis; Galactosemias; Genetic Testing; Histidine; Humans; Infant; Infant, Newborn; Metabolism, Inborn Errors; Phenylketonurias; Tay-Sachs Disease; United Kingdom | 1974 |
[Screening results for inborn errors of metabolism in Western Europe].
Topics: Denmark; Europe; Evaluation Studies as Topic; France; Galactosemias; Germany, West; Histidine; Homocystinuria; Humans; Infant, Newborn; International Cooperation; Ireland; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Netherlands; Phenylketonurias; Preventive Medicine; Switzerland; Tyrosine; United Kingdom | 1973 |
Collective results of mass screening for inborn metabolic errors in eight European countries.
Topics: Belgium; Denmark; France; Galactosemias; Germany, West; Histidine; Homocystinuria; Humans; Infant, Newborn; Ireland; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Netherlands; Phenylketonurias; Switzerland; Tyrosine; United Kingdom | 1973 |
Genetic screening: notes added in proof.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Cystathionine; Galactosemias; Genetics, Population; Histidine; Humans; Infant; Infant, Newborn; Maple Syrup Urine Disease; Mass Screening; Phenylalanine; Phenylketonurias; Succinates | 1973 |
Austria newborn screening programme for inborn errors of metabolism.
Topics: Austria; Female; Galactosemias; Histidine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Sex Factors | 1973 |
Letter: Frequency of some metabolic disorders in Poland.
Topics: Biological Assay; Galactosemias; Histidine; Humans; Infant, Newborn; Mass Screening; Phenylalanine; Phenylketonurias; Poland; Tyrosine | 1974 |
[Studies on the frequencies of inborn errors of metabolism in Eastern and Western Austria].
Topics: Austria; Chromatography; Clinical Enzyme Tests; Galactosemias; Gene Frequency; Genetics, Population; Histidine; Humans; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Probability | 1972 |
[5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report].
Topics: Amino Acid Metabolism, Inborn Errors; Austria; Child, Preschool; Chromatography, Thin Layer; Diet Therapy; Economics, Medical; Follow-Up Studies; Galactosemias; Glycine; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Metal Metabolism, Inborn Errors; Multiphasic Screening; Phenylketonurias; Proline; Time Factors; Tyrosine | 1972 |
[Early diagnosis of congenital metabolic diseases].
Topics: Diet Therapy; Galactosemias; Histidine; Homocystinuria; Humans; Hyperglycemia; Infant, Newborn; Leucine; Lipoproteins; Lysine; Metabolism, Inborn Errors; Phenylketonurias; Time Factors; Valine | 1971 |
Inborn metabolic disorders with associated ocular lesions in Northern Ireland.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Cataract; Child; Child, Preschool; Cornea; Eye Diseases; Female; Galactosemias; Hepatolenticular Degeneration; Histidine; Homocystinuria; Humans; Infant; Lens, Crystalline; Male; Myopia; Northern Ireland; Pigmentation Disorders; Renal Aminoacidurias | 1967 |
[Austrian programm for the early detection of inborn errors of metabolism].
Topics: Austria; Child, Preschool; Female; Galactosemias; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Male; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias | 1970 |
[Current views on therapy of some dysmetabolic oligophrenias].
Topics: Child, Preschool; Diet Therapy; Galactosemias; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Intellectual Disability; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine | 1967 |
[Early recognition of congenital metabolic disorders].
Topics: Galactosemias; Histidine; Humans; Infant, Newborn; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Phenylketonurias | 1968 |