phenylalanine and Infant, Newborn, Diseases

phenylalanine has been researched along with Infant, Newborn, Diseases in 79 studies

Research

Studies (79)

Timeframe	Studies, this research(%)	All Research%
pre-1990	76 (96.20)	18.7374
1990's	2 (2.53)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (1.27)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Akiyama, M; Suga, Y; Sugiura, K	1
ARMSTRONG, MD; BINKLEY, EL	1
GUTHRIE, R; SUSI, A	1
BERMAN, JL; HSIA, DY; SLATIS, HM	1
PARTINGTON, MW; SINNOTT, B	1
FLEMING, W; NOTRICASIN, HR	1
ALT, EJ; DORSEY, DC; JENSEN, RL; SOLOMS, G	1
Cawley, LP; Dibbern, P; Goodwin, WL	1
Hudson, FP	1
Antonozzi, I; De Giorgis, GF; Del Castello, PG; Loizzo, A; Rosano, M	1
Castro, JV; Norton, PM; Sansaricq, C; Snyderman, SE	1
Dhondt, JL; Farriaux, JP	1
Levy, HL; Mitchell, ML	1
Clemens, P; Grüttner, R; Plettner, C	1
Schneider, AJ	1
Corbeel, L	1
McCabe, ER; McCabe, L	1
Dóber, I; Klujber, L; Mestyán, J; Schultz, K; Soltész, G	1
Stroud, HW; Tenbrinck, MS	1
Knoll, E; Scheibenreiter, S; Schön, R; Thalhammer, O; Wehle, E	1
Paunier, L	1
Alm, J; Larsson, A	1
Friedman, EG; Koch, R	1
Hayde, M; Lubec, G; Menzel, D; Pollak, A; Widness, JA	1
Gebre-Medhin, M; Larsson, U; Lindblad, BS; Zetterström, R	1
Brown, DA; Connelly, J; Francis, I; Hill, G; Masters, P; McFarlane, J; Pitt, D; Raby, J; Tucker, RG; Wilcken, B	1
Rodríguez Alarcón, J; Sanjurjo, P; Vallo, A	1
Dilger, J; Peters, FD; Roemer, VM	1
Woody, NC	1
Briard, ML; du Fraysseix, M; Rapoport, D; Rey, F; Rey, J	1
Rey, F; Rey, J	1
Enzenauer, J; Matz, D; Menne, F	1
Koepp, P	1
Güttler, F; Wamberg, E	1
Alm, J; Holmgren, G; Larsson, A; Palmstierna, H	1
Holub, J; Hoza, J; Hyánek, J; Karger, P; Simková, M; Viletová, H	1
Abrosimova, NA; Barashnev, IuI; Chicherin, LP; Dukarskiĭ, FG; Pesnia, VV	1
Alvarez Domínguez, L; Campistol Plana, J; Castillo Rivera, P; Maya Victoria, A; Prats Coll, R; Riverola de Veciana, AT	1
Hsia, DY	1
Bremer, HJ; Przyrembel, H	1
Nothjunge, J	1
Adams, B; McIntire, MS	1
Janssen, EG	1
Saugstad, LF	1
Cunningham, GC; Dontanville, VK	1
Blaton, V; Lievens-Taveirne, J; Peeters, H; Vercaemst, R	1
Thalhammer, O	1
Holtzman, NA; Kallman, CH; Mellits, ED	1
Holtzman, NA; Kallman, CH; Meek, AG; Mellits, ED	1
Svatý, J	1
Snyder, MJ; Woodward, TE	1
Linneweh, F	1
Howell, RR; Stevenson, RE	1
Berman, JL; Blumenfeld, CM; Pildes, RS	1
Smith, BA; Waisman, HA	1
Berry, HK; Hunt, MM; Sutherland, BS	1
Curtius, HC; Gitzelmann, R; Rampini, S	1
Schön, R; Thalhammer, O	1
Bosshard, HR; Curtius, HC; Müller, M; Rampini, S; Völlmin, JA	1
Becroft, DM; Horn, CR	1
O'Halloran, MT; Stuckey, SJ; Yu, JS	1
Cabalska, B; Duczyńska, N; Wnuk, W	1
Babin, JP; Hehunstre, JP; Marc, Y; Martin, C; Navarro, C; San Juan, B	1
Komrower, GM	1
Schmidt, H	1
Hagge, W; Irtel von Brenndorff, A	1
Humbel, R; Kutter, D	1
Woolf, LI	1
Cahalane, SF	1
Carré, IJ; Carson, NA; Neill, DW	1
Partington, MW	1
Nitschké, E	1
Egorov, NS; Khokhlov, AP	1
Day, RW; Kleinman, DS; Twiss, S	1
Bickel, H	1

Reviews

7 review(s) available for phenylalanine and Infant, Newborn, Diseases

Article	Year
[Diagnosis and therapy of 6 inherited, metabolic diseases, leading to mental deficiency. 1]. Medizinische Klinik, 1976, Apr-23, Volume: 71, Issue:17 Topics: Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Heterozygote; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intelligence Tests; Mass Screening; Mental Disorders; Phenylalanine; Phenylketonurias; Tyrosine	1976
[Transitory disorders of amino acid metabolism. Practical viewpoints]. Monatsschrift fur Kinderheilkunde, 1973, Volume: 121, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Ascorbic Acid; Cystathionine; Diagnosis, Differential; Histidine; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Infant, Premature, Diseases; Male; Metabolic Diseases; Methionine; Milk Proteins; Phenylalanine; Rats; Testicular Diseases; Time Factors; Tyrosine	1973
[Clinico-chemical symptom: hyperphenylalaninemia]. Hippokrates, 1974, Volume: 45, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Diet Therapy; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Phenylalanine; Phenylketonurias; Prognosis; Syndrome	1974
Hyperphenylalaninemia and pregnancy. Nutrition reviews, 1972, Volume: 30, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Child; Female; Haplorhini; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Intelligence Tests; Male; Mass Screening; Microcephaly; Phenylalanine; Pregnancy; Pregnancy Complications	1972
[Problems around phenylketonuria]. Ceskoslovenska pediatrie, 1969, Volume: 24, Issue:8 Topics: Diet Therapy; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Intelligence Tests; Phenylalanine; Phenylketonurias; Tyrosine	1969
The clinical use of chloramphenicol. The Medical clinics of North America, 1970, Volume: 54, Issue:5 Topics: Anemia, Aplastic; Chemical Phenomena; Chemistry; Chloramphenicol; Eye Diseases; Female; Hematologic Diseases; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infections; Melioidosis; Phenylalanine; Pregnancy; Respiratory Tract Infections; Rickettsia Infections; Salmonella Infections; Sepsis; Tularemia	1970
The offspring of phenylketonuric women. Social biology, 1971, Volume: 18 Topics: Abortion, Spontaneous; Adult; Birth Weight; Black or African American; Brain Chemistry; Breast Feeding; Child, Preschool; Congenital Abnormalities; Diet Therapy; Female; Glutamine; Heart Auscultation; Heterozygote; Hexokinase; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Intelligence Tests; Male; Maryland; Microcephaly; Myelin Sheath; Nerve Tissue Proteins; Phenylacetates; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Prenatal Care; Pyruvate Kinase; Umbilical Cord	1971

Other Studies

72 other study(ies) available for phenylalanine and Infant, Newborn, Diseases

Article	Year
Very mild lamellar ichthyosis with compound heterozygous TGM1 mutations including the novel missense mutation p.Leu693Phe. Journal of dermatological science, 2013, Volume: 72, Issue:2 Topics: Amino Acid Sequence; Arginine; Base Sequence; DNA Mutational Analysis; Heterozygote; Humans; Ichthyosis, Lamellar; Infant; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Male; Molecular Sequence Data; Mutation; Mutation, Missense; Phenylalanine; Prognosis; Protein Structure, Tertiary; Sequence Homology, Amino Acid; Transglutaminases	2013
Studies on phenylketonuria. V. Observations on a newborn infant with phenylketonuria. Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 1956, Volume: 93, Issue:3 Topics: Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias	1956
A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS. Pediatrics, 1963, Volume: 32 Topics: Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Phenylalanine; Phenylketonurias	1963
SCREENING NEWBORN INFANTS FOR PHENYLKETONURIA. JAMA, 1964, Apr-20, Volume: 188 Topics: Biomedical Research; Blood Chemical Analysis; Humans; Illinois; Infant; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Neonatal Screening; Phenylalanine; Phenylketonurias; Statistics as Topic	1964
CASE FINDING IN PHENYLKETONURIA. II. THE GUTHRIE TEST. Canadian Medical Association journal, 1964, Jul-18, Volume: 91 Topics: Bacteriological Techniques; Biological Assay; Canada; Clinical Laboratory Techniques; Filtration; Hematologic Tests; Hospitalization; Hospitals; Hospitals, Psychiatric; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Laboratories; Mass Screening; Paper; Phenylalanine; Phenylketonurias; Prisons; Urine	1964
BLOOD PHENYLALANINE LEVELS OF NEWBORN INFANTS. A ROUTINE SCREENING PROGRAM FOR THE HOSPITAL NEWBORN NURSERY. California medicine, 1964, Volume: 101 Topics: Blood; Brain Injuries; Clinical Laboratory Techniques; Hospitals; Hospitals, Community; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Laboratories; Life; Mass Screening; Nurseries, Hospital; Phenylalanine; Phenylketonurias	1964
THE GUTHRIE TEST IN MONITORING THE DIET IN PKU: AN APPRAISAL OF ITS APPLICABILITY. Clinical pediatrics, 1965, Volume: 4 Topics: Blood Chemical Analysis; Diet; Diet Therapy; Electrocardiography; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Monitoring, Physiologic; Phenylalanine; Phenylketonurias	1965
One-dimensional paper chromatography of serum amino acids, with particular reference to phenylalanine. American journal of clinical pathology, 1967, Volume: 48, Issue:4 Topics: Amino Acids; Chromatography, Paper; Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias	1967
Phenylketonuria. Proceedings of the Royal Society of Medicine, 1967, Nov-01, Volume: 60, Issue:11 Part 1 Topics: Diet Therapy; Dietary Proteins; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Intelligence; Intelligence Tests; Male; Mass Screening; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications	1967
EEG as a possible prognostic tool in phenylketonuria. Electroencephalography and clinical neurophysiology, 1983, Volume: 55, Issue:1 Topics: Brain; Electroencephalography; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias; Prognosis	1983
Routine neonatal screening for phenylketonuria in the United Kingdom 1964-78. Medical Research Council Steering Committee for the MRC/DHSS Phenylketonuria Register. British medical journal (Clinical research ed.), 1981, May-23, Volume: 282, Issue:6277 Topics: False Negative Reactions; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Phenylalanine; Phenylketonurias; Registries; United Kingdom	1981
Plasma and cerebrospinal fluid amino acid concentrations in phenylketonuria during the newborn period. The Journal of pediatrics, 1981, Volume: 99, Issue:1 Topics: Amino Acids; Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias; Threonine; Tyrosine	1981
Hepatic phenylalanine hydroxylase activity in hyperphenylalaninaemia. Journal of inherited metabolic disease, 1981, Volume: 4, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Humans; Infant, Newborn; Infant, Newborn, Diseases; Liver; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias	1981
The current status of newborn screening. Hospital practice (Office ed.), 1982, Volume: 17, Issue:7 Topics: Bacteriological Techniques; Blood Specimen Collection; Congenital Hypothyroidism; Humans; Hypothyroidism; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Phenylalanine; Phenylketonurias; Thyrotropin; Thyroxine; United States	1982
[Phenylketonuria screening: false-positive and false-negative results]. Deutsche medizinische Wochenschrift (1946), 1983, Apr-22, Volume: 108, Issue:16 Topics: False Negative Reactions; False Positive Reactions; Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias	1983
Newborn phenylalanine/tyrosine metabolism. Implications for screening for phenylketonuria. American journal of diseases of children (1960), 1983, Volume: 137, Issue:5 Topics: Aging; Fetal Blood; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Tyrosine	1983
[Problems posed by maternal phenylketonuria]. Archives francaises de pediatrie, 1983, Volume: 40 Suppl 1 Topics: Brain; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tryptophan; Tyrosine	1983
Screening for PKU in sick or premature neonates. The Journal of pediatrics, 1983, Volume: 103, Issue:3 Topics: Humans; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature, Diseases; Phenylalanine; Phenylketonurias	1983
Metabolic effects of septicaemia in newborn and young infants with particular reference to the plasma free amino acids. Acta paediatrica Academiae Scientiarum Hungaricae, 1980, Volume: 21, Issue:4 Topics: Alanine; Amino Acids; Amino Acids, Branched-Chain; Bacterial Infections; Escherichia coli Infections; Glycine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Proline; Pseudomonas Infections; Sepsis; Tyrosine	1980
Normal infant born to a mother with phenylketonuria. JAMA, 1982, Apr-16, Volume: 247, Issue:15 Topics: Adult; Child, Preschool; Female; Fetal Diseases; Follow-Up Studies; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Maternal-Fetal Exchange; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Pregnancy Trimester, First	1982
[12 years Austrian newborn screening for inborn errors of metabolism. Results with special reference to phenylketonuria, hyperphenylalaninemia and histidinemia (author's transl)]. Klinische Padiatrie, 1980, Volume: 192, Issue:6 Topics: Austria; Female; Histidine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Male; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Psychometrics	1980
[Detections tests for newborn infants]. Revue medicale de la Suisse romande, 1981, Volume: 101, Issue:5 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. 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
Accuracy of newborn screening programs for phenylketonuria. The Journal of pediatrics, 1981, Volume: 98, Issue:2 Topics: Fetal Blood; Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias	1981
Hydroxyl radical generation in oxygen-treated infants. Pediatrics, 1997, Volume: 100, Issue:4 Topics: Apgar Score; Dose-Response Relationship, Drug; Humans; Hydroxyl Radical; Infant, Newborn; Infant, Newborn, Diseases; Oxygen; Oxygen Inhalation Therapy; Phenylalanine; Regression Analysis; Tyrosine	1997
Subclinical protein-energy malnutrition in under-privileged Ethiopian mothers and their newborn infants. Acta paediatrica Scandinavica, 1978, Volume: 67, Issue:2 Topics: Adolescent; Adult; Developing Countries; Ethiopia; Female; Fetal Blood; Glycine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Isoleucine; Methionine; Phenylalanine; Pregnancy; Pregnancy Complications; Protein-Energy Malnutrition; Socioeconomic Factors; Tyrosine; Valine	1978
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
[Hypophenylalaninemia in dietary treatment of phenylketonuria (author's transl)]. Anales espanoles de pediatria, 1978, Volume: 11, Issue:3 Topics: Diet Therapy; Female; Humans; Iatrogenic Disease; Infant; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias	1978
[Treatment of diabetes during pregnancy with Des-Phe insulin: preliminary results (author's transl)]. Deutsche medizinische Wochenschrift (1946), 1979, Jul-06, Volume: 104, Issue:27 Topics: Adult; Female; Humans; Hyperinsulinism; Infant, Newborn; Infant, Newborn, Diseases; Insulin; Insulin Antibodies; Phenylalanine; Pregnancy; Pregnancy in Diabetics	1979
What to do with the Guthrie test report. The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society, 1978, Volume: 130, Issue:5 Topics: Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Mass Screening; Phenylalanine; Phenylketonurias; Tyrosine	1978
[Results after 5 years of early treated phenyketonuria. Correlations with the quality of dietetic control]. Archives francaises de pediatrie, 1978, Volume: 35, Issue:10 Suppl Topics: Age Factors; Child Development; Female; Follow-Up Studies; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intelligence Tests; Male; Phenylalanine; Phenylketonurias; Sex Factors; Time Factors	1978
[Phenylketonuria and mental development: a badly stated problem]. Archives francaises de pediatrie, 1978, Volume: 35, Issue:10 Suppl Topics: Age Factors; Child Development; Follow-Up Studies; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intelligence Tests; Phenylalanine; Phenylketonurias; Time Factors	1978
[Phenylalanine metabolites in the urine after oral phenylalanine loading. Significance for the discrimination between classical phenylketonuria and variations of hyperphenylalaninemia (heterozygotes and homozygotes)]. Fortschritte der Medizin, 1977, Mar-10, Volume: 95, Issue:10 Topics: Administration, Oral; Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Genetic Variation; Heterozygote; Homozygote; Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias	1977
On indications for treatment of the hyperphenylalaninemic neonate. Acta paediatrica Scandinavica, 1977, Volume: 66, Issue:3 Topics: Denmark; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Mass Screening; Phenylalanine; Phenylketonurias; Tyrosine	1977
The frequency of PKU and hyperphenylalaninemia in Sweden - a study in institutions for the mentally retarded as well as in neonates. Clinical genetics, 1976, Volume: 10, Issue:6 Topics: Adolescent; Adult; Aged; Child; Hospitals, Special; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Middle Aged; Phenylalanine; Phenylketonurias; Sweden	1976
[Clinical diagnosis of hyperphenylalaninemia in the newborn infant and infant stages]. Ceskoslovenska pediatrie, 1976, Volume: 31, Issue:11 Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias	1976
Results of the examination of newborn infants for phenylketonuria and histidinemia in Moscow. Pediatriia, 1975, Issue:5 Topics: Child Health Services; Female; Histidine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Moscow; Phenylalanine; Phenylketonurias	1975
[Follow up protocol of patients with hyperphenylalaninemia]. Anales espanoles de pediatria, 1990, Volume: 33, Issue:5 Topics: Follow-Up Studies; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Phenylalanine; Phenylketonurias	1990
The aminoacidopathies. Monographs in human genetics, 1972, Volume: 6 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
PKU testing in Omaha-Douglas County. The Nebraska medical journal, 1972, Volume: 57, Issue:3 Topics: Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Nebraska; Phenylalanine; Phenylketonurias	1972
[Clinical test of the adapted infant's rady-to-eat lactic food Pre-Aptamil]. Monatsschrift fur Kinderheilkunde, 1973, Volume: 121, Issue:2 Topics: Apgar Score; Ascorbic Acid; Birth Weight; Body Weight; Diet Therapy; Female; Food Preservation; Histidine; Humans; Infant Food; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Isoleucine; Leucine; Lysine; Male; Methionine; Phenylalanine; Threonine; Tryptophan; Valine	1973
Increased "reproductive casualty" in heterozygotes for phenylketonuria. Clinical genetics, 1973, Volume: 4, Issue:2 Topics: Abortion, Spontaneous; Birth Weight; Delivery, Obstetric; Embryonic and Fetal Development; Female; Fetal Death; Heterozygote; Humans; Infant Mortality; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Labor Presentation; Male; Obstetric Labor Complications; Parity; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Uterine Hemorrhage	1973
Effect of feeding on screening for PKU in infants. Pediatrics, 1973, Volume: 51, Issue:3 Topics: Age Factors; Animals; Breast Feeding; False Negative Reactions; Follow-Up Studies; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Milk; Milk, Human; Phenylalanine; Phenylketonurias; Time Factors	1973
Screening for hyperaminoacidemias in newborns by thin-layer chromatography on DEAE-cellulose. Acta paediatrica Belgica, 1973, Volume: 27, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Belgium; Chromatography, DEAE-Cellulose; Chromatography, Thin Layer; Humans; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Mass Screening; Methods; Phenylalanine; Tyrosine; Valine	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
Neonatal screening for phenylketonuria. II. Age dependence of initial phenylalanine in infants with PKU. Pediatrics, 1974, Volume: 53, Issue:3 Topics: Age Factors; Female; Follow-Up Studies; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Mass Screening; Ontario; Phenylalanine; Phenylketonurias; Quebec; Time Factors; United States	1974
Neonatal screening for phenylketonuria. 3. Altered sex ratio; extent and possible causes. The Journal of pediatrics, 1974, Volume: 85, Issue:2 Topics: Age Factors; Female; Follow-Up Studies; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Mass Screening; Phenylalanine; Phenylketonurias; Public Health Administration; Regression Analysis; Sex Factors; Surveys and Questionnaires; United States	1974
[Isotope use in the study of hereditary metabolic diseases]. Monatsschrift fur Kinderheilkunde, 1970, Volume: 118, Issue:6 Topics: Animals; Autoradiography; Blood Glucose; Brain Chemistry; Carbon Isotopes; Chromatography, Paper; Deficiency Diseases; Feces; Galactose; Glucokinase; Glucose; Glycosuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Malabsorption Syndromes; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Radioisotope Dilution Technique; Radioisotopes; Rats; Tritium	1970
Effect of protein loading on blood phenylalanine levels in newborn infants. Acta paediatrica Scandinavica, 1972, Volume: 61, Issue:3 Topics: Animals; Densitometry; Dietary Proteins; Female; Fluorometry; Humans; Infant Food; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Male; Milk; Phenylalanine; Phenylketonurias	1972
Leucine equivalency system in managing branched chain ketoaciduria. Journal of the American Dietetic Association, 1971, Volume: 59, Issue:4 Topics: Amino Acids; Chemical Phenomena; Chemistry; Diet; Diet Therapy; Female; Food Analysis; Growth; Humans; Infant Food; Infant, Newborn; Infant, Newborn, Diseases; Isoleucine; Keto Acids; Leucine; Maple Syrup Urine Disease; Methods; Phenylalanine; Time Factors; Valine	1971
Nutritional management in phenylketonuria. American journal of diseases of children (1960), 1971, Volume: 122, Issue:1 Topics: Amino Acids; Child; Child Development; Child Nutritional Physiological Phenomena; Child, Preschool; Diet Therapy; Dietary Proteins; Feeding Behavior; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Nutritional Requirements; Phenylalanine; Phenylketonurias	1971
[Phenylketonuria and hyperphenylalaninemia]. Helvetica paediatrica acta, 1971, Volume: 25 Topics: Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias	1971
[Routine thin-layer-chromatography in 25000 newborn infants. Comparison with the Guthrie-tests]. Zeitschrift fur Kinderheilkunde, 1971, Volume: 111, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, Thin Layer; Histidine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Mass Screening; Methionine; Methods; Phenylalanine; Tyrosine	1971
Determination of urinary aromatic acids by gas chromatography. Results from healthy infants and from patients with phenylketonuria. Zeitschrift fur klinische Chemie und klinische Biochemie, 1971, Volume: 9, Issue:5 Topics: Child; Child, Preschool; Chromatography, Gas; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias; Tyrosine	1971
The Guthrie screening test for phenylketonuria: a report on two years participation in the national programme. The New Zealand medical journal, 1969, Volume: 69, Issue:443 Topics: Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Methods; New Zealand; Phenylalanine; Phenylketonurias; State Medicine; Tyrosine	1969
The dangers of dietary therapy in phenylketonuria. The Medical journal of Australia, 1970, Aug-29, Volume: 2, Issue:9 Topics: Deficiency Diseases; Diet Therapy; Edema; Fatigue; Feeding and Eating Disorders; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Neurologic Manifestations; Phenylalanine; Phenylketonurias; Sucking Behavior; Vomiting	1970
The incidence of phenylketonuria and evaluation of its early treatment. Polish medical journal, 1969, Volume: 8, Issue:5 Topics: Child Development; Diet Therapy; Dietary Proteins; Follow-Up Studies; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Phenylalanine; Phenylketonurias; Poland	1969
[A case of phenylketonuria detected at birth. Favorable course thanks to the diet]. Archives francaises de pediatrie, 1970, Volume: 27, Issue:5 Topics: Diet Therapy; Female; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias	1970
Phenylketonuria. Some current problems. Archives of disease in childhood, 1970, Volume: 45, Issue:239 Topics: Biological Assay; Cerebral Cortex; Chromatography; Diet Therapy; Fluorometry; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intelligence; Lipids; Phenylalanine; Phenylketonurias; Time Factors	1970
[Treatment of phenylketonuria]. Deutsche medizinische Wochenschrift (1946), 1970, Feb-20, Volume: 95, Issue:8 Topics: Animals; Chromatography, Thin Layer; Diagnosis, Differential; Diet Therapy; Humans; Indicators and Reagents; Infant; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Milk; Phenylalanine; Phenylketonurias	1970
[Spicular formation of the radius metaphysis as a manifestation of phenylalanine deficiency]. Monatsschrift fur Kinderheilkunde, 1970, Volume: 118, Issue:6 Topics: Anemia; Body Weight; Calcinosis; Deficiency Diseases; Diet Therapy; Female; Growth Disorders; Hand; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Male; Nutritional Requirements; Phenylalanine; Phenylketonurias; Radiography; Radius; Ulna	1970
[Systematic screening for phenylketonuria with Phenistix]. Das Medizinische Laboratorium, 1967, Volume: 20, Issue:12 Topics: Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenotype; Phenylalanine; Phenylketonurias	1967
Screening tests for phenylketonuria. British medical journal, 1968, Mar-16, Volume: 1, Issue:5593 Topics: Diet Therapy; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Phenylalanine; Phenylketonurias	1968
Population screening by Guthrie test for phenylketonuria in South-east Scotland. Report by the consultant paediatricians and medical officers of health of the S.E. Scotland Hospital Region. British medical journal, 1968, Mar-16, Volume: 1, Issue:5593 Topics: Blood Specimen Collection; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Phenylalanine; Phenylketonurias; Scotland	1968
Mass screening of the newborn for metabolic disease. Archives of disease in childhood, 1968, Volume: 43, Issue:228 Topics: Automation; Diet Therapy; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; United Kingdom; United States	1968
Phenylketonuria. Mass screening of newborns in Ireland. Archives of disease in childhood, 1968, Volume: 43, Issue:228 Topics: Chromatography; Humans; Infant, Newborn; Infant, Newborn, Diseases; Ireland; Mass Screening; Phenylalanine; Phenylketonurias; Tyrosine	1968
Results of routine screening for phenylketonuria in early infancy, Northern Ireland (1960-67). Archives of disease in childhood, 1968, Volume: 43, Issue:228 Topics: Chlorides; Filtration; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Iron; Mass Screening; Northern Ireland; Phenylalanine; Phenylketonurias	1968
Case-finding in phenylketonuria: 3. One-way paper chromatography of amino acids in blood. Canadian Medical Association journal, 1968, Oct-05, Volume: 99, Issue:13 Topics: Amino Acids; Chromatography, Paper; Humans; Infant, Newborn; Infant, Newborn, Diseases; Methods; Phenylalanine; Phenylketonurias; Tyrosine	1968
[Thin layer chromatography separation and semi-quantitative determination of blood phenylalanine as procedure for the systematic screening of phenylketonuria in newborn infants]. Zeitschrift fur klinische Chemie und klinische Biochemie, 1968, Volume: 6, Issue:3 Topics: Chromatography, Thin Layer; Humans; Infant, Newborn; Infant, Newborn, Diseases; Methods; Phenylalanine; Phenylketonurias	1968
[Excretion of phenylacetylglutamine in the newborn with birth trauma, intrauterine hypotrophy and hemolytic disease]. Pediatriia, 1968, Volume: 6 Topics: Birth Injuries; Congenital Abnormalities; Erythroblastosis, Fetal; Female; Fetal Diseases; Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Pregnancy	1968
Some factors affecting McCaman-Robins test results in screening newborns for PKU. Pediatrics, 1966, Volume: 38, Issue:4 Topics: Blood Specimen Collection; California; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Phenylalanine; Phenylketonurias; Specimen Handling	1966
[Early diagnosis of phenylketonuria]. Monatsschrift fur Kinderheilkunde, 1966, Volume: 114, Issue:1 Topics: Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias	1966