phenylalanine has been researched along with Stunted Growth in 21 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (61.90) | 18.7374 |
| 1990's | 4 (19.05) | 18.2507 |
| 2000's | 1 (4.76) | 29.6817 |
| 2010's | 3 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Álvarez de la Campa, E; Colobran, R; de la Cruz, X; Martín-Nalda, A; Martínez-Gallo, M; Pujol-Borrell, R; Soler-Palacín, P | 1 |
| Bélanger-Quintana, A; Blau, N; Demirkol, M; Feillet, F; Giovannini, M; MacDonald, A; Trefz, FK; van Spronsen, FJ | 1 |
| Hosoki, K; Saitoh, S; Sudo, A; Takeichi, N | 1 |
| Debrabander, A; Dobbelaere, D; Farriaux, JP; Gottrand, F; Michaud, L; Turck, D; Vanderbecken, S | 1 |
| Benevenga, NJ; Steele, RD | 1 |
| Bartley, J; Beuhler, B; Lipson, A; O'Halloran, M; Walsh, D; Webster, W; Yu, J | 1 |
| Doesburg, WH; Sengers, RC; van der Schot, LW | 1 |
| Acosta, PB; Yannicelli, S | 1 |
| Borrow, P; de la Torre, JC; Oldstone, MB; Teng, MN | 1 |
| Johnson, RC; Shah, SN | 1 |
| Halliday, D; Pacy, PJ; Thompson, GN; Watts, RW | 1 |
| O'Halloran, MT; Yu, JS | 1 |
| Daftari, B; Fishman, MA; Prensky, AL | 1 |
| Bost, M; Boucharlat, J; Favier, A; Ledru, J; Ratel, M; Serre, JC | 1 |
| Berry, HK; Light, IJ; Sutherland, JM | 1 |
| Benevenga, NJ; Harper, AE; Wohlhueter, RM | 1 |
| Hsia, DY | 1 |
| Ballester, L; Callens, G; Callens, M; Duquennoy, C; Gaudier, B; Ponté, C | 1 |
| Davidson, W; Hanley, WB; Linsao, L; Moes, CA | 1 |
| Hagge, W; Irtel von Brenndorff, A | 1 |
| Ersser, RS; Harries, JT; Lloyd, JK; Seakins, JW | 1 |
3 review(s) available for phenylalanine and Stunted Growth
| Article | Year |
|---|---|
Adverse effects of excessive consumption of amino acids.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Brain; Cattle; Diet; Disease Models, Animal; Ethionine; Fenclonine; Glycine; Growth Disorders; Histidine; Humans; Methionine; Nerve Tissue Proteins; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Pneumonia, Atypical Interstitial, of Cattle; Serine; Stereoisomerism; Sulfhydryl Compounds; Tissue Distribution; Tryptophan; Tyrosine; Vitamin A | 1984 |
Effects of ingestion of disproportionate amounts of amino acids.
Topics: Adaptation, Physiological; Age Factors; Amino Acids; Ammonia; Animals; Cystine; Deficiency Diseases; Feeding Behavior; Glycine; Growth Disorders; Histidine; Homeostasis; Humans; Leucine; Liver; Lysine; Methionine; Nicotinic Acids; Nutrition Disorders; Phenylalanine; Rats; Threonine; Tryptophan; Tyrosine | 1970 |
Phenylketonuria and its variants.
Topics: Adult; Child, Preschool; Congenital Abnormalities; Female; Gene Frequency; Growth Disorders; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Middle Aged; Mixed Function Oxygenases; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine | 1970 |
2 trial(s) available for phenylalanine and Stunted Growth
| Article | Year |
|---|---|
Evaluation of nutritional status and pathophysiology of growth retardation in patients with phenylketonuria.
Topics: Aging; Anthropometry; Body Composition; Body Height; Body Weight; Child; Child, Preschool; Chromatography, Gas; Cross-Sectional Studies; Diet; Erythrocytes; Female; Growth Disorders; Hormones; Humans; Insulin-Like Growth Factor Binding Protein 3; Insulin-Like Growth Factor I; Male; Nutritional Status; Phenylalanine; Phenylketonurias; Thyroid Hormones; Trace Elements; Tyrosine | 2003 |
Protein intake affects phenylalanine requirements and growth of infants with phenylketonuria.
Topics: Dietary Proteins; Energy Metabolism; Growth Disorders; Humans; Infant; Infant Food; Nutritional Requirements; Phenylalanine; Phenylketonurias | 1994 |
16 other study(ies) available for phenylalanine and Stunted Growth
| Article | Year |
|---|---|
Clinical and structural impact of mutations affecting the residue Phe367 of FOXP3 in patients with IPEX syndrome.
Topics: Diabetes Mellitus, Type 1; Diarrhea; Dimerization; Eczema; Eosinophilia; Fatal Outcome; Forkhead Transcription Factors; Genetic Diseases, X-Linked; Growth Disorders; Hemorrhage; Hepatomegaly; Humans; Hydrophobic and Hydrophilic Interactions; Immune System Diseases; Immunoglobulin E; Infant; Klebsiella Infections; Leukocytosis; Lung Diseases; Male; Meningoencephalitis; Models, Molecular; Mutation; Phenylalanine; Sepsis; Splenomegaly; Thrombocytopenia; Thymus Gland | 2016 |
Challenges and pitfalls in the management of phenylketonuria.
Topics: Biopterins; Brain; Cognition Disorders; Consensus; Growth Disorders; Humans; Infant, Newborn; Neonatal Screening; Neuropsychological Tests; Phenylalanine; Phenylketonurias; Treatment Failure | 2010 |
Successful cochlear implantation in a patient with mitochondrial hearing loss and m.625G>A transition.
Topics: Audiometry, Pure-Tone; Brain; Child; Cochlear Implantation; Electron Transport Complex III; Epilepsy, Generalized; Female; Genome, Mitochondrial; Growth Disorders; Hearing Loss, Sensorineural; Humans; Hypertrichosis; Lactates; Magnetic Resonance Imaging; Mitochondria; Mitochondrial Diseases; Phenylalanine; Point Mutation; RNA, Transfer; Treatment Outcome | 2011 |
Maternal hyperphenylalaninemia fetal effects.
Topics: Adolescent; Adult; Child; Congenital Abnormalities; Face; Female; Fetal Growth Retardation; Growth Disorders; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Microcephaly; Phenylalanine; Pregnancy; Pregnancy Complications; Strabismus | 1984 |
The phenylalanine response curve in relation to growth and mental development in the first year of life.
Topics: Child, Preschool; Developmental Disabilities; Growth Disorders; Humans; Infant; Infant, Newborn; Phenylalanine; Phenylketonurias | 1994 |
A single amino acid change in the glycoprotein of lymphocytic choriomeningitis virus is associated with the ability to cause growth hormone deficiency syndrome.
Topics: Animals; Cell Line; Cricetinae; Genetic Variation; Glycoproteins; Growth Disorders; Hypoglycemia; Lymphocytic choriomeningitis virus; Mice; Mice, Inbred C3H; Phenylalanine; Reassortant Viruses; Serine; Syndrome; Viral Proteins | 1996 |
Effect of postweaning hyperphenylalaninemia on brain development in rats: myelination, lipid, and fatty acid composition of myelin.
Topics: Animals; Animals, Suckling; Brain; Cerebrosides; Fatty Acids; Fenclonine; Growth Disorders; Myelin Sheath; Phenylalanine; Rats; Sphingomyelins; Sulfoglycosphingolipids | 1978 |
Protein metabolism in phenylketonuria and Lesch-Nyhan syndrome.
Topics: Adolescent; Adult; Amino Acids; Female; Growth Disorders; Humans; Lesch-Nyhan Syndrome; Leucine; Male; Middle Aged; Phenylalanine; Phenylketonurias; Proteins | 1990 |
Children of mothers with phenylketonuria.
Topics: Adolescent; Adult; Child; Child, Preschool; Diet Therapy; Family Planning Services; Female; Growth Disorders; Heart Defects, Congenital; Heterozygote; Homozygote; Humans; Intellectual Disability; Male; Microcephaly; Middle Aged; Phenylalanine; Phenylketonurias; Seizures; Strabismus; Tyrosine | 1970 |
Recovery of rat brain from a brief hyperphenylalaninemic insult early in development.
Topics: Age Factors; Animals; Body Weight; Brain; Disease Models, Animal; DNA; Growth Disorders; Humans; Lipid Metabolism; Nerve Tissue Proteins; Organ Size; Phenylalanine; Phenylketonurias; Rats; Rats, Inbred Strains; RNA | 1974 |
[2 new cases of microcephalic children with intrauterine growth retardation born of phenylketonuric mothers].
Topics: Birth Weight; Chromatography, Ion Exchange; Female; Growth Disorders; Humans; Infant; Male; Mental Disorders; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine | 1972 |
Clinical significance of tyrosinemia of prematurity.
Topics: Amino Acid Metabolism, Inborn Errors; Ascorbic Acid; Child Development; Chromatography, Paper; Diet Therapy; Fatigue; Feeding Behavior; Female; Growth Disorders; Humans; Infant, Newborn; Infant, Premature, Diseases; Intelligence; Intelligence Tests; Phenylalanine; Pregnancy; Pregnancy Complications; Tyrosine | 1973 |
[Delayed intrauterine growth with microcephaly in 3 children born of a hyperphenylalaninemic mother].
Topics: Abortion, Spontaneous; Adult; Child; Child, Preschool; Congenital Abnormalities; Diet Therapy; Female; Fetal Diseases; Growth Disorders; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Microcephaly; Pedigree; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications, Hematologic | 1972 |
Malnutrition with early treatment of phenylketonuria.
Topics: Anemia; Bone Diseases, Developmental; Child, Preschool; Deficiency Diseases; Diet Therapy; Growth Disorders; Humans; Hypoproteinemia; Infant; Intellectual Disability; Nutrition Disorders; Phenylalanine; Phenylketonurias | 1970 |
[Spicular formation of the radius metaphysis as a manifestation of phenylalanine deficiency].
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 |
Recovery after dietary treatment of an infant with features of tyrosinosis.
Topics: Amino Acid Metabolism, Inborn Errors; Cholestasis; Diet Therapy; Female; Growth Disorders; Humans; Hypophosphatemia, Familial; Infant; Methionine; Phenylalanine; Phosphates; Renal Aminoacidurias; Rickets; Tyrosine | 1969 |