tryptophan has been researched along with Hypogonadism in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Ashourvan, A; Bassett, DS; Cao, W; Epperson, CN; Gur, RC; Loughead, J; Ruparel, K; Sammel, MD; Satterthwaite, TD; Shanmugan, S | 1 |
| Nawata, H; Nishi, Y; Oba, K; Ohe, K; Takayanagi, R; Yanase, T | 1 |
| Freire-Maia, N | 1 |
3 other study(ies) available for tryptophan and Hypogonadism
| Article | Year |
|---|---|
Impact of childhood adversity on network reconfiguration dynamics during working memory in hypogonadal women.
Topics: Adverse Childhood Experiences; Behavior; Brain; Brain Mapping; Child; Cohort Studies; Executive Function; Female; Humans; Hypogonadism; Magnetic Resonance Imaging; Memory, Short-Term; Menopause; Middle Aged; Nerve Net; Neural Pathways; Neuronal Plasticity; Neuropsychological Tests; Tryptophan | 2020 |
New mutations of DAX-1 genes in two Japanese patients with X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism.
Topics: Adolescent; Adrenal Insufficiency; Base Sequence; Codon; DAX-1 Orphan Nuclear Receptor; DNA-Binding Proteins; Exons; Genetic Linkage; Humans; Hypogonadism; Japan; Male; Molecular Sequence Data; Mutation; Pedigree; Polymerase Chain Reaction; Receptors, Retinoic Acid; Repressor Proteins; Sequence Analysis, DNA; Transcription Factors; Tryptophan; X Chromosome | 1996 |
A newly recognized genetic syndrome of tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities.
Topics: Abnormalities, Multiple; Adolescent; Adult; Alopecia; Animals; Brazil; Breast; Child; Cleft Lip; Cleft Palate; Ear Deformities, Acquired; Ectodermal Dysplasia; Ectromelia; Electrocardiography; Electroencephalography; Growth Disorders; Heart Function Tests; Humans; Hypogonadism; Infant, Newborn; Intellectual Disability; Limb Deformities, Congenital; Male; Pedigree; Sibling Relations; Skin Abnormalities; Thyroid Gland; Tooth Abnormalities; Tryptophan | 1970 |