Page last updated: 2024-08-17

histidine and Classic Galactosemia

histidine has been researched along with Classic Galactosemia in 30 studies

Research

Studies (30)

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

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

Reviews

3 review(s) available for histidine and Classic Galactosemia

Article	Year
Neonatal screening tests. Pediatric clinics of North America, 1980, Volume: 27, Issue:4 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. Clinics in perinatology, 1976, Volume: 3, Issue:1 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. 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

Other Studies

27 other study(ies) available for histidine and Classic Galactosemia

Article	Year
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM. Journal of the Irish Medical Association, 1964, Volume: 54 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. European journal of pediatrics, 1984, Volume: 142, Issue:3 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. Human heredity, 1984, Volume: 34, Issue:1 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. Medical decision making : an international journal of the Society for Medical Decision Making, 1982, Volume: 2, Issue:1 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. Acta paediatrica Scandinavica, 1981, Volume: 70, Issue:5 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]. Fortschritte der Medizin, 1978, Jun-22, Volume: 96, Issue:24 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]. MMW, Munchener medizinische Wochenschrift, 1979, Jun-22, Volume: 121, Issue:25 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]. Medizinische Klinik, 1976, Apr-30, Volume: 71, Issue:18 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. The Medical journal of Australia, 1979, May-05, Volume: 1, Issue:9 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]. La Clinica terapeutica, 1979, Mar-15, Volume: 88, Issue:5 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. Pediatrics, 1978, Volume: 61, Issue:5 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]. Monatsschrift fur Kinderheilkunde, 1976, Volume: 129, Issue:9 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. 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
Outcome of the patients detected by newborn screening in Japan. Acta paediatrica Japonica : Overseas edition, 1988, Volume: 30, Issue:4 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. Journal of clinical pathology. Supplement (Royal College of Pathologists), 1974, Volume: 8 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]. Monatsschrift fur Kinderheilkunde, 1973, Volume: 121, Issue:5 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. Acta paediatrica Scandinavica, 1973, Volume: 62, Issue:4 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. Advances in human genetics, 1973, Volume: 4 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. Acta Universitatis Carolinae. Medica. Monographia, 1973, Volume: 56 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. Acta paediatrica Scandinavica, 1974, Volume: 63, Issue:3 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]. Humangenetik, 1972, Volume: 15, Issue:2 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]. Wiener klinische Wochenschrift, 1972, Volume: 84 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]. Minerva medica, 1971, Nov-03, Volume: 62, Issue:83 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. Transactions of the ophthalmological societies of the United Kingdom, 1967, Volume: 87 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]. Wiener klinische Wochenschrift, 1970, Jan-02, Volume: 82, Issue:1 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]. Minerva pediatrica, 1967, Dec-22, Volume: 19, Issue:51 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]. Hippokrates, 1968, Feb-15, Volume: 39, Issue:3 Topics: Galactosemias; Histidine; Humans; Infant, Newborn; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Phenylketonurias	1968