tryptophan has been researched along with Genetic Diseases, X-Chromosome Linked in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aznar-Laín, G; Gonzalez-Sepulveda, M; Gracia-Rubio, I; Marcos, J; Pérez-Jurado, LA; Pozo, OJ; Renau, N; Segura, J; Valverde, O; Ventura, R | 1 |
| Murthy, AS | 1 |
| CREPALDI, G; PARPAJOLA, A | 1 |
| HARRIS, JW; HORRIGAN, DL | 1 |
| Clark, RD; Friez, MJ; Graham, JM; Jones, JR; Joseph, SM; May, M; Moeschler, JB; Opitz, JM; Peiffer, AP; Risheg, H; Rogers, RC; Schwartz, CE; Stevenson, RE | 1 |
2 review(s) available for tryptophan and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
X-linked hypophosphatemic rickets and craniosynostosis.
Topics: Bone Remodeling; Bone Transplantation; Calcification, Physiologic; Cranial Sutures; Craniosynostoses; Craniotomy; Exons; Familial Hypophosphatemic Rickets; Fibroblast Growth Factor-23; Fibroblast Growth Factors; Follow-Up Studies; Genetic Diseases, X-Linked; Homeostasis; Humans; Infant, Newborn; Intracranial Hypertension; Male; Mutation; Occipital Bone; Parietal Bone; PHEX Phosphate Regulating Neutral Endopeptidase; Tryptophan | 2009 |
PYRIDOXINE-RESPONSIVE ANEMIA: ANALYSIS OF 62 CASES.
Topics: Amino Acids; Anemia; Anemia, Hypochromic; Anemia, Macrocytic; Anemia, Sideroblastic; Drug Therapy; Erythropoiesis; Genetic Diseases, X-Linked; Humans; Iron; Pathology; Prognosis; Pyridoxine; Tryptophan; Vitamin B 6 Deficiency | 1964 |
3 other study(ies) available for tryptophan and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
Targeting tryptophan and tyrosine metabolism by liquid chromatography tandem mass spectrometry.
Topics: Adult; Aged; Aggression; Animals; Chromatography, Liquid; Disruptive, Impulse Control, and Conduct Disorders; Female; Genetic Diseases, X-Linked; Healthy Volunteers; Humans; Intellectual Disability; Kynurenic Acid; Kynurenine; Male; Mice; Middle Aged; Monoamine Oxidase; Prefrontal Cortex; Serotonin; Tandem Mass Spectrometry; Tryptophan; Tyrosine; Young Adult | 2016 |
EXCRETION OF TRYPTOPHAN METABOLITES IN DIFFERENT FORMS OF HAEMOBLASTOSIS.
Topics: Cortisone; Cyclophosphamide; Genetic Diseases, X-Linked; Hodgkin Disease; Humans; Kynurenic Acid; Kynurenine; Leukemia; Leukemia, Hairy Cell; Leukemia, Lymphoid; Leukemia, Myeloid; Lymphatic Diseases; Lymphoma; Lymphoma, Large B-Cell, Diffuse; Lymphoma, Non-Hodgkin; Mechlorethamine; Multiple Myeloma; ortho-Aminobenzoates; Phenylbutazone; Polycythemia Vera; Proteins; Pyridoxal Phosphate; Pyridoxine; Sarcoma; Severe Combined Immunodeficiency; Tryptophan; Urine; Xanthurenates | 1964 |
A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome.
Topics: Amino Acid Substitution; Arginine; Family; Female; Genetic Diseases, X-Linked; Humans; Intellectual Disability; Male; Mediator Complex; Muscle Hypotonia; Mutation; Pedigree; Receptors, Thyroid Hormone; Syndrome; Tryptophan | 2007 |