tryptophan has been researched along with Infant, Newborn, Diseases in 17 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 15 (88.24) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (5.88) | 29.6817 |
| 2010's | 1 (5.88) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ashcroft, AS; Ashcroft, FM; Ellard, S; Hattersley, AT; Männikkö, R; Sansom, MS; Stansfeld, PJ | 1 |
| WALDINGER, C | 1 |
| MURTAGH, JJ; RAPPALLINI, C | 1 |
| Aittoniemi, J; Ashcroft, FM; de Wet, H; Flanagan, SE; Hattersley, AT; Lafond, M; Pearson, ER; Proks, P; Sansom, MS | 1 |
| Careddu, P; Schwarz-Tiene, E | 1 |
| Corbeel, L | 1 |
| Bhagavan, NV; Scottolini, AG; Woo, P | 1 |
| Deacon-Smith, RA; Kamuzora, H; Lee-Potter, JP; Lehmann, H; Simpkiss, MJ | 1 |
| Bürger, U; Meissner, S; Wolf, H | 1 |
| Anderson, GM; Cohen, DJ; Hoder, EL; Shaywitz, BA | 1 |
| Heine, W; Kellner, R | 1 |
| Hardy, J; Heeley, AF; Heeley, ME; Soothill, JF | 1 |
| Chiancone, FM; Mainardi, L; Tenconi, LT | 1 |
| Allegri, G; Costa, C; De Antoni, A; Rubaltelli, FF | 1 |
| Janssen, EG | 1 |
| Milstein, JM; Swaiman, KF | 1 |
| Grosser, V; Hinkel, GK; Kintzel, HW; Knapp, A | 1 |
17 other study(ies) available for tryptophan and Infant, Newborn, Diseases
| Article | Year |
|---|---|
A conserved tryptophan at the membrane-water interface acts as a gatekeeper for Kir6.2/SUR1 channels and causes neonatal diabetes when mutated.
Topics: Amino Acid Sequence; Animals; ATP-Binding Cassette Transporters; Cell Membrane; Child; Conserved Sequence; Diabetes Mellitus; Female; Genetic Carrier Screening; Humans; Infant, Newborn; Infant, Newborn, Diseases; Molecular Sequence Data; Mutation; Oocytes; Phenotype; Potassium Channels, Inwardly Rectifying; Rats; Receptors, Drug; Sulfonylurea Receptors; Tryptophan; Xenopus laevis | 2011 |
PRIDOXINE DEFICIENCY AND PYRIDOXINE DEPENDENCY IN INFANTS AND CHILDREN.
Topics: Biochemical Phenomena; Biochemistry; Child; Epilepsy; Female; Genetics, Medical; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Metabolism; Pregnancy; Pyridoxine; Seizures; Tryptophan; Vitamin B 6 Deficiency | 1964 |
[SEROTONIN AND 5-HYDROXYINDOLACETIC ACID IN THE NEWBORN INFANT].
Topics: Anemia; Anemia, Aplastic; Cardiovascular System; Gastrointestinal Tract; Humans; Hydroxyindoleacetic Acid; Indoleacetic Acids; Infant; Infant, Newborn; Infant, Newborn, Diseases; Metabolic Diseases; Metabolism; Nervous System; Pellagra; Phenylketonurias; Physiology; Renal Aminoacidurias; Respiratory System; Serotonin; Tryptophan | 1964 |
A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetes.
Topics: Adenosine Diphosphate; Adenosine Triphosphatases; Adenosine Triphosphate; Amino Acid Sequence; Amino Acid Substitution; Arginine; ATP-Binding Cassette Transporters; Child; Diabetes Mellitus; Humans; Infant, Newborn; Infant, Newborn, Diseases; Ion Channel Gating; Kinetics; Male; Molecular Sequence Data; Mutant Proteins; Mutation; Potassium Channels, Inwardly Rectifying; Protein Structure, Secondary; Protein Structure, Tertiary; Receptors, Drug; Sulfonylurea Receptors; Tryptophan | 2008 |
[Quantitative determination of urinary metabolites of the tryptophan-nicotinic acid line in the urine of children with febrile cramps and infantile spasms].
Topics: Aminobutyrates; Fever; Humans; Infant, Newborn; Infant, Newborn, Diseases; Nicotinic Acids; Spasm; Tryptophan; Vitamin B 6 Deficiency | 1967 |
[Problems posed by maternal phenylketonuria].
Topics: Brain; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tryptophan; Tyrosine | 1983 |
Vitamin B6 responsive infantile convulsions and branched chain amino aciduria.
Topics: Adult; Amino Acids, Branched-Chain; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Pyridoxine; Seizures; Tryptophan | 1978 |
A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine.
Topics: Amino Acid Sequence; Anemia, Hemolytic; Diseases in Twins; Fetal Hemoglobin; Glycine; Hemoglobins, Abnormal; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Tryptophan | 1975 |
[Investigations on the utilisation of parenterally administered amino acids by premature and small-for-dates neonates. II. Investigations of elimination half life time, elimination constants, transfer and clearances of amino acids after short-time infusi
Topics: Age Factors; Amino Acids; Arginine; Female; Glomerular Filtration Rate; Glutamates; Half-Life; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Injections, Intravenous; Male; Ornithine; Sex Factors; Time Factors; Tryptophan | 1975 |
Neurotransmitter precursors and metabolites in CSF of human neonates.
Topics: Female; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Indoleacetic Acids; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Male; Methoxyhydroxyphenylglycol; Neurotransmitter Agents; Reference Values; Tryptophan; Tyrosine | 1985 |
[Vitamin B6 requirement of infants in parenteral feeding with amino acid mixtures].
Topics: Amino Acids; Buttocks; Dermatitis, Exfoliative; Facial Dermatoses; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infusions, Parenteral; Nutritional Requirements; Pyridoxine; Scalp Dermatoses; Tryptophan; Xanthurenates | 1969 |
A disorder of tryptophan metabolism in chronic granulomatous disease.
Topics: Child; Child, Preschool; Chromatography, Paper; Chronic Disease; Granuloma; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infections; Kynurenic Acid; Kynurenine; Lymphadenitis; Male; Niacinamide; Pyridoxine; Tryptophan; Xanthurenates | 1970 |
[Tryptophan metabolism in screening metabolic diseases of the newborn].
Topics: Amino Acid Metabolism, Inborn Errors; Evaluation Studies as Topic; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Liver; Mass Screening; Metabolism, Inborn Errors; Methods; Niacinamide; Pregnancy; Tryptophan; Tryptophan Oxygenase | 1973 |
Urinary excretion of tryptophan metabolites during phototherapy.
Topics: Aminohippuric Acids; Humans; Hydroxyindoleacetic Acid; Hyperbilirubinemia; Infant, Newborn; Infant, Newborn, Diseases; Kynurenic Acid; Kynurenine; ortho-Aminobenzoates; Photochemistry; Phototherapy; Serotonin; Tryptophan; Xanthurenates | 1974 |
[Clinical test of the adapted infant's rady-to-eat lactic food Pre-Aptamil].
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 |
Pyridoxine dependency and penicillamine.
Topics: Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Kidney Function Tests; Penicillamine; Phenobarbital; Pyridoxine; Seizures; Tryptophan | 1970 |
[Vitamin-B6-dependent pediatric diseases. Hereditary pyridoxine-dependent spasms in newborns and xanthurenuria in parents].
Topics: Adult; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Metabolism, Inborn Errors; Pregnancy; Pyridoxine; Seizures; Tryptophan; Vitamin B 6 Deficiency; Xanthurenates | 1970 |