Page last updated: 2024-08-17

histidine and Classic Galactosemia

histidine has been researched along with Classic Galactosemia in 30 studies

Research

Studies (30)

TimeframeStudies, this research(%)All Research%
pre-199030 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
COFFEY, VP1
Aoki, K; Arashima, S; Kawamura, M; Kitagawa, T; Oura, T; Sakai, K; Suwa, S; Tada, K; Takesada, M; Tateda, H1
Yasuda, N1
Alm, J; Larsson, A; Rosenqvist, U1
Mamunes, P2
Alm, J; Larsson, A1
Schmid-Rüter, E2
Krüger, M; Menne, F; Otte, HJ; Winterhoff, D1
Enzenauer, J; Matz, D; Menne, F1
Hill, GN; Pollard, AC; Robertson, EF1
Menne, F1
Davidow, B; Goldberg, D; Grossi, M; Grover, R; Shahidi, S; Wethers, D1
Bickel, H1
Aoki, K; Wada, Y1
Clayton, BE1
Levy, HL2
Thalhammer, O1
Bozkowa, K; Cabalska, MB1
Scheiber, V; Thalhammer, O1
Knoll, E; Scheibenreiter, S; Schmierer, G; Schön, R; Thalhammer, O1
Steuer, W1
Carson, NA; Martin, VA1
Biedl, E; Scheibenreiter, S; Thalhammer, O1
Giovannini, M1
Bauer, B1

Reviews

3 review(s) available for histidine and Classic Galactosemia

ArticleYear
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

ArticleYear
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