phenylalanine has been researched along with Galactosemias in 24 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 22 (91.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (8.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Murphy, E | 1 |
| Allen, J; Bonham, J; Casbolt, AM; Downing, M; Ellin, S; Maloney, M; Race, G; Shakespeare, L | 1 |
| BICKEL, H | 2 |
| Aoki, K; Arashima, S; Kawamura, M; Kitagawa, T; Oura, T; Sakai, K; Suwa, S; Tada, K; Takesada, M; Tateda, H | 1 |
| Hassemer, DJ; Hoffman, GL; Laessig, RH; Makowski, ER | 1 |
| Mamunes, P | 1 |
| Paunier, L | 1 |
| Alm, J; Larsson, A | 1 |
| Knapp, A | 1 |
| Omenn, GS | 1 |
| Aoki, K; Wada, Y | 1 |
| Henderson, MJ; McCowan, C; Shapiro, L | 1 |
| Roth, KS | 1 |
| Raine, DN | 1 |
| Hsia, DY | 1 |
| Royer, P | 1 |
| Levy, HL | 2 |
| Thalhammer, O | 1 |
| Bozkowa, K; Cabalska, MB | 1 |
| Dahlqvist, A; Jagenburg, R; Mark, A | 1 |
| Scheiber, V; Thalhammer, O | 1 |
| Hill, JB; Hochella, NJ | 1 |
4 review(s) available for phenylalanine and Galactosemias
| Article | Year |
|---|---|
Medical Problems in Obstetrics: Inherited Metabolic Disease.
Topics: Abortion, Spontaneous; Breast Feeding; Developmental Disabilities; Female; Galactosemias; Humans; Infertility, Female; Metabolism, Inborn Errors; Nausea; Phenylalanine; Phenylketonuria, Maternal; Postnatal Care; Preconception Care; Pregnancy; Pregnancy Complications; Teratogenesis; Vomiting | 2015 |
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 |
Inborn errors of metabolism: clues to understanding human behavioral disorders.
Topics: Adrenal Hyperplasia, Congenital; Brain; Galactosemias; Glycine; Hepatolenticular Degeneration; Heterozygote; Homocystinuria; Humans; Lesch-Nyhan Syndrome; Maple Syrup Urine Disease; Mental Disorders; Metabolism, Inborn Errors; Mucopolysaccharidoses; Phenylalanine; Phenylketonurias; Porphyrias; Sphingolipidoses; Turner Syndrome; Urea | 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 |
20 other study(ies) available for phenylalanine and Galactosemias
| Article | Year |
|---|---|
Elevated phenylalanine on newborn screening: follow-up testing may reveal undiagnosed galactosaemia.
Topics: Galactosemias; Humans; Infant, Newborn; Neonatal Screening; Phenylalanine; Phenylketonurias | 2010 |
[Diagnosis and therapy of galactosemia and phenylketonuria].
Topics: Blood; Body Fluids; Galactose; Galactosemias; Humans; Phenylalanine; Phenylketonurias; Urine | 1955 |
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 |
Dual-channel continuous-flow system for determination of phenylalanine and galactose: application to newborn screening.
Topics: Autoanalysis; Galactosemias; Humans; Infant, Newborn; Mass Screening; Phenylalanine | 1984 |
[Detections tests for newborn infants].
Topics: Amino Acid Metabolism, Inborn Errors; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Methionine; Phenylalanine | 1981 |
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 |
[Problems and results of screening tests in genetic disorders].
Topics: Cystic Fibrosis; Galactosemias; Genetic Diseases, Inborn; Humans; Hypothyroidism; Infant, Newborn; Mass Screening; Phenylalanine; Phenylketonurias; Pilot Projects; Risk | 1978 |
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 |
Galactosemia detection from phenylketonuria screening.
Topics: Female; Galactosemias; Humans; Infant, Newborn; Mass Screening; Phenylalanine; Phenylketonurias | 1988 |
Newborn metabolic screening: a search for "nature's experiments".
Topics: Biopterins; Galactosemias; Homocystinuria; Humans; Infant, Newborn; Keto Acids; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Thiamine; Time Factors; United States | 1986 |
Differential diagnosis and treatment of hyperphenylalaninaemia.
Topics: Acid-Base Equilibrium; Amino Acids; Biopterins; Diagnosis, Differential; Galactosemias; Humans; Hydrogen-Ion Concentration; Infant, Newborn; Maple Syrup Urine Disease; Mass Screening; Phenylalanine; Phenylketonurias | 1985 |
Inherited metabolic disease.
Topics: Albumins; Amino Acid Metabolism, Inborn Errors; Chromatography; Clinical Laboratory Techniques; Costs and Cost Analysis; Cystic Fibrosis; Evaluation Studies as Topic; Galactosemias; Genetic Counseling; Humans; Hyperlipidemias; Infant; Infant, Newborn; Iron; Mass Screening; Meconium; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias | 1974 |
The aminoacidopathies.
Topics: Amino Acid Metabolism, Inborn Errors; Cells, Cultured; Clone Cells; Culture Techniques; Female; Fibroblasts; Galactosemias; Genes, Recessive; Heterozygote; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Mucopolysaccharidoses; Phenylalanine; Phenylketonurias; Sex Factors | 1972 |
[Dietetics in hereditary enzyme deficiencies].
Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Diarrhea, Infantile; Diet Therapy; Galactosemias; Homocystinuria; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Isoleucine; Leucine; Maple Syrup Urine Disease; Methionine; Phenylalanine; Phenylketonurias; Tyrosine; Valine | 1970 |
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 |
A patient with hereditary galactosemia studied with a screening method for galactose in urine.
Topics: Amino Acids; Cerebrospinal Fluid; Chromatography, Paper; Diet Therapy; Electroencephalography; Erythrocytes; Exchange Transfusion, Whole Blood; Galactose; Galactosemias; Glycosuria; Humans; Infant; Infant, Newborn; Male; Methods; Parenteral Nutrition; Phenylalanine; RNA Nucleotidyltransferases; Spinal Puncture; Time Factors | 1969 |
[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 |
Fluorometric screening procedure for galactosemia utilizing the autoanalyzer.
Topics: Autoanalysis; Equipment and Supplies; Female; Fluorometry; Galactose; Galactosemias; Humans; Indicators and Reagents; Infant, Newborn; Male; Mass Screening; Methods; Nucleotidyltransferases; Phenylalanine; Time Factors | 1969 |