tryptophan has been researched along with Acrocephaly in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Murthy, AS | 1 |
| Cohen, MM | 1 |
| Anderson, PJ; Cox, TC; David, DJ; Netherway, DJ; Roscioli, T | 1 |
| Nakakita, N; Sakai, N; Sakata, Y; Shida, H; Susami, T; Takato, T; Tokunaga, K; Uchinuma, E; Yamazaki, Y | 1 |
2 review(s) available for tryptophan and Acrocephaly
| 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 |
Unclassifiable craniosynostosis phenotypes, FGFR2 Trp290 mutations, acanthosis nigricans, and unpaired cysteine mutations.
Topics: Acanthosis Nigricans; Amino Acid Substitution; Craniosynostoses; Cysteine; Humans; Phenotype; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 2; Receptors, Fibroblast Growth Factor; Tryptophan | 2002 |
2 other study(ies) available for tryptophan and Acrocephaly
| Article | Year |
|---|---|
Do Craniosynostosis syndrome phenotypes with both FGFR2 and TWIST mutations have a worse clinical outcome?
Topics: Acrocephalosyndactylia; Adenine; Adolescent; Arginine; Child, Preschool; Craniofacial Dysostosis; Craniosynostoses; Cysteine; Cytosine; DNA Transposable Elements; Female; Follow-Up Studies; Guanine; Humans; Male; Mutation; Receptor, Fibroblast Growth Factor, Type 2; Sequence Deletion; Serine; Syndrome; Thymine; Treatment Outcome; Tryptophan; Twist-Related Protein 1 | 2006 |
Sequence analysis of fibroblast growth factor receptor 2 ( FGFR2 ) in Japanese patients with craniosynostosis.
Topics: Acrocephalosyndactylia; Arginine; Cleft Palate; Codon; Craniofacial Dysostosis; Craniosynostoses; Exons; Female; Heterozygote; Humans; Japan; Male; Mutation; Polymerase Chain Reaction; Proline; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 2; Receptors, Fibroblast Growth Factor; Sequence Analysis, DNA; Serine; Syndactyly; Tryptophan | 2001 |