phenylalanine and Developmental Disabilities

phenylalanine has been researched along with Developmental Disabilities in 22 studies

Research

Studies (22)

Timeframe	Studies, this research(%)	All Research%
pre-1990	4 (18.18)	18.7374
1990's	4 (18.18)	18.2507
2000's	10 (45.45)	29.6817
2010's	3 (13.64)	24.3611
2020's	1 (4.55)	2.80

Authors

Authors	Studies
Çıkı, K; Dursun, A; Özgül, RK; Pektaş, E; Sivri, HS; Tokatlı, A; Yıldız, Y; Yücel Yılmaz, D	1
Murphy, E	1
Baudin, J; Lee, PJ; Lilburn, M; Maillot, F; Morley, DW	1
Ben Dridi, MF; Dhondt, JL; El Asmi, M; Feki, M; Jemaa, R; Kaabachi, N; Khemir, S; Mebazaa, A; Sanhaji, H; Tebib, N	1
Duvekot, JJ; Hop, WC; Prick, BW	1
Hartfield, DS; Yager, JY	1
Gurry, D; Ng, TW; Rae, A; Wray, J; Wright, H	1
Azen, C; Rouse, B	1
Cockburn, F; Lee, PJ; Ridout, D; Walter, JH	1
Blau, N; Connolly, MB; Demos, MK; Hyland, K; Lillquist, Y; Makhseed, N; Vallance, HD; Waters, PJ	1
Agostoni, C; Cockburn, F; Demellweek, C; Giovannini, M; Harkness, RA; Harvie, A; McCulloch, DL; Murray, G; Riva, E	1
Chang, M; He, C; Hsiao, KJ; Liu, TT; Shen, M; Shen, S; Wang, L; Yu, WM; Zhang, Z; Zhou, Z	1
Doesburg, WH; Sengers, RC; van der Schot, LW	1
Allred, E; Azen, C; Chang, P; de la Cruz, F; Hanley, W; Koch, R; Levy, HL; Matalon, R; Rouse, B; Shifrin, H; Waisbren, SE	1
Dhondt, JL; Mikaeloff, Y; Pinton, F; Ponsot, G; Sevin, C	1
Azen, C; de la Cruz, F; Hanley, W; Koch, R; Levy, H; Matalon, R; Rouse, B; Trefz, F	1
Huntington, K; Mandernach, T; Nortz, MJ; Steiner, RD; White, DA	1
Brown, ES; Warner, R	1
Lyon, IC; Macfarlane, SD; Pullon, DH	1
Ball, PA; Booth, IW; Edwards, MA; Green, A; Morgan, I; Puntis, JW	1
Buttè, C; Giovannini, M; Longhi, R; Paccanelli, S; Riva, E; Valsasina, R	1
Davidson, W; Hackney, IM; Hanley, WB; Lindsao, L	1

Reviews

3 review(s) available for phenylalanine and Developmental Disabilities

Article	Year
Medical Problems in Obstetrics: Inherited Metabolic Disease. Best practice & research. Clinical obstetrics & gynaecology, 2015, Volume: 29, Issue:5 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
Maternal phenylketonuria and hyperphenylalaninemia in pregnancy: pregnancy complications and neonatal sequelae in untreated and treated pregnancies. The American journal of clinical nutrition, 2012, Volume: 95, Issue:2 Topics: Congenital Abnormalities; Developmental Disabilities; Facial Bones; Female; Humans; Infant, Newborn; Infant, Small for Gestational Age; Intellectual Disability; Microcephaly; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Pregnancy Complications; Pregnancy Outcome; Pregnancy Trimesters; Skull	2012
Neurologic manifestations of iron deficiency in childhood. Pediatric neurology, 2002, Volume: 27, Issue:2 Topics: Anemia, Iron-Deficiency; Brain Diseases; Child; Child, Preschool; Developmental Disabilities; Dopamine; gamma-Aminobutyric Acid; Humans; Infant; Iron Deficiencies; Phenylalanine; Pseudotumor Cerebri; Serotonin; Stroke	2002

Trials

1 trial(s) available for phenylalanine and Developmental Disabilities

Article	Year
A randomized trial of long-chain polyunsaturated fatty acid supplementation in infants with phenylketonuria. Developmental medicine and child neurology, 2006, Volume: 48, Issue:3 Topics: Developmental Disabilities; Double-Blind Method; Evoked Potentials, Visual; Fatty Acids, Unsaturated; Female; Humans; Infant; Male; Phenylalanine; Phenylketonurias; Prospective Studies	2006

Other Studies

18 other study(ies) available for phenylalanine and Developmental Disabilities

Article	Year
DNACJ12 deficiency in patients with unexplained hyperphenylalaninemia: two new patients and a novel variant. Metabolic brain disease, 2021, Volume: 36, Issue:6 Topics: Amino Acid Metabolism, Inborn Errors; Biopterins; Child; Developmental Disabilities; Female; Genetic Variation; HSP40 Heat-Shock Proteins; Humans; Infant, Newborn; Intellectual Disability; Male; Muscle Hypotonia; Neurotransmitter Agents; Phenylalanine; Phenylalanine Hydroxylase; Protein Isoforms	2021
Factors influencing outcomes in the offspring of mothers with phenylketonuria during pregnancy: the importance of variation in maternal blood phenylalanine. The American journal of clinical nutrition, 2008, Volume: 88, Issue:3 Topics: Body Weight; Developmental Disabilities; Female; Humans; Infant, Newborn; Learning Disabilities; Microcephaly; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Pregnancy Complications; Retrospective Studies; Treatment Outcome	2008
Phenylketonuria is still a major cause of mental retardation in Tunisia despite the possibility of treatment. Clinical neurology and neurosurgery, 2011, Volume: 113, Issue:9 Topics: Age of Onset; Amino Acids; Child, Preschool; Developmental Disabilities; Female; Gas Chromatography-Mass Spectrometry; Health Services Accessibility; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Neonatal Screening; Phenylalanine; Phenylketonurias; Pigmentation Disorders; Retrospective Studies; Speech Disorders; Tunisia	2011
Maternal phenylketonuria in Western Australia: pregnancy outcomes and developmental outcomes in offspring. Journal of paediatrics and child health, 2003, Volume: 39, Issue:5 Topics: Child Behavior; Child Development; Child, Preschool; Cognition; Developmental Disabilities; Female; Hospitals, Maternity; Humans; Infant; Infant, Newborn; Longitudinal Studies; Male; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Pregnancy Outcome; Risk Factors; Western Australia	2003
Effect of high maternal blood phenylalanine on offspring congenital anomalies and developmental outcome at ages 4 and 6 years: the importance of strict dietary control preconception and throughout pregnancy. The Journal of pediatrics, 2004, Volume: 144, Issue:2 Topics: Abnormalities, Multiple; Child; Child, Preschool; Cognition; Developmental Disabilities; Diet, Protein-Restricted; Face; Female; Fetal Growth Retardation; Gestational Age; Heart Defects, Congenital; Humans; Infant; Infant, Newborn; Intelligence Tests; Microcephaly; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Pregnancy Outcome; Prenatal Care	2004
Maternal phenylketonuria: report from the United Kingdom Registry 1978-97. Archives of disease in childhood, 2005, Volume: 90, Issue:2 Topics: Analysis of Variance; Birth Weight; Child; Child, Preschool; Cognition Disorders; Developmental Disabilities; Female; Head; Heart Defects, Congenital; Humans; Infant, Newborn; Intelligence; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Registries; Time Factors; United Kingdom	2005
6-pyruvoyl-tetrahydropterin synthase deficiency with mild hyperphenylalaninemia. Annals of neurology, 2005, Volume: 58, Issue:1 Topics: 5-Hydroxytryptophan; Biopterins; Carbidopa; Cerebral Palsy; Child; Developmental Disabilities; Diagnostic Errors; Dopamine Agents; Female; Humans; Levodopa; Movement Disorders; Phenylalanine; Phenylketonurias; Phosphorus-Oxygen Lyases; Seizures	2005
Long-term outcome and neuroradiological findings of 31 patients with 6-pyruvoyltetrahydropterin synthase deficiency. Journal of inherited metabolic disease, 2006, Volume: 29, Issue:1 Topics: Brain; Brain Diseases, Metabolic, Inborn; Child, Preschool; Developmental Disabilities; Female; Humans; Infant; Magnetic Resonance Imaging; Male; Nervous System Diseases; Phenylalanine; Phosphorus-Oxygen Lyases; Time Factors; Treatment Outcome	2006
The phenylalanine response curve in relation to growth and mental development in the first year of life. Acta paediatrica (Oslo, Norway : 1992). Supplement, 1994, Volume: 407 Topics: Child, Preschool; Developmental Disabilities; Growth Disorders; Humans; Infant; Infant, Newborn; Phenylalanine; Phenylketonurias	1994
Neonatal neurological assessment of offspring in maternal phenylketonuria. Journal of inherited metabolic disease, 1998, Volume: 21, Issue:1 Topics: Developmental Disabilities; Female; Follow-Up Studies; Humans; Infant, Newborn; Male; Neurologic Examination; Neuropsychological Tests; Phenylalanine; Phenylketonuria, Maternal; Pregnancy	1998
[Progressive convulsive encephalopathy: considering a abnormality of biopterin metabolism]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 1999, Volume: 6, Issue:7 Topics: 5-Hydroxytryptophan; Algeria; Anticonvulsants; Biopterins; Brain; Child, Preschool; Consanguinity; Developmental Disabilities; Diet Therapy; Epilepsy; France; Humans; Levodopa; Magnetic Resonance Imaging; Male; Neopterin; Phenylalanine; Phenylketonurias	1999
Maternal phenylketonuria syndrome: congenital heart defects, microcephaly, and developmental outcomes. The Journal of pediatrics, 2000, Volume: 136, Issue:1 Topics: Adult; Child Development; Cohort Studies; Developmental Disabilities; Diet; Female; Follow-Up Studies; Genotype; Gestational Age; Heart Defects, Congenital; Humans; Infant, Newborn; Intelligence; Medical Records; Microcephaly; Mutation; Phenylalanine; Phenylketonurias; Preconception Care; Pregnancy; Pregnancy Complications; Psychomotor Performance; Risk Factors; Ultrasonography, Prenatal	2000
Age-related working memory impairments in children with prefrontal dysfunction associated with phenylketonuria. Journal of the International Neuropsychological Society : JINS, 2002, Volume: 8, Issue:1 Topics: Adolescent; Age Factors; Analysis of Variance; Case-Control Studies; Child; Cognition; Developmental Disabilities; Female; Humans; Male; Memory, Short-Term; Neuropsychological Tests; Phenylalanine; Phenylketonurias; Prefrontal Cortex	2002
Mental development of phenylketonuric children on or off diet after the age of six. Psychological medicine, 1976, Volume: 6, Issue:2 Topics: Adolescent; Child; Developmental Disabilities; Female; Humans; Intelligence; Male; Phenylalanine; Phenylketonurias	1976
Maternal phenylketonuria. The New Zealand medical journal, 1990, Aug-22, Volume: 103, Issue:896 Topics: Child; Child, Preschool; Developmental Disabilities; Diseases in Twins; Female; Humans; Infant; Intellectual Disability; Intelligence; Male; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy	1990
Hyperphenylalaninaemia in parenterally fed newborn babies. Lancet (London, England), 1986, Nov-08, Volume: 2, Issue:8515 Topics: Developmental Disabilities; Humans; Infant, Newborn; Male; Parenteral Nutrition; Phenylalanine	1986
Cranial computerized tomography in dihydropteridine reductase deficiency. Journal of inherited metabolic disease, 1985, Volume: 8, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Atrophy; Basal Ganglia Diseases; Brain Diseases; Calcinosis; Developmental Disabilities; Female; Humans; Infant; NADH, NADPH Oxidoreductases; Phenylalanine; Phenylketonurias; Tomography, X-Ray Computed	1985
Phenylketonuria: mental development, behavior, and termination of low phenylalanine diet. The Journal of pediatrics, 1968, Volume: 72, Issue:5 Topics: Adolescent; Age Factors; Autistic Disorder; Child Behavior Disorders; Developmental Disabilities; Diet Therapy; Follow-Up Studies; Humans; Infant; Infant, Newborn; Intellectual Disability; Intelligence Tests; Phenylalanine; Phenylketonurias; Psychological Tests	1968