Found: 14
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Genetic Variants of Steroidogenesis and Gonadotropin Pathways and Polycystic Ovary Syndrome Susceptibility: A Systematic Review and Meta-analysis.
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- Metabolic Syndrome & Related Disorders, 2024, v. 22, n. 1, p. 15, doi. 10.1089/met.2023.0127
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- Article
Maternal candidate gene variants, epigenetic factors, and susceptibility to idiopathic recurrent pregnancy loss: A systematic review.
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- International Journal of Gynecology & Obstetrics, 2023, v. 162, n. 3, p. 829, doi. 10.1002/ijgo.14701
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- Article
Genetic Determinants of Selenium Availability, Selenium-Response, and Risk of Polycystic Ovary Syndrome.
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- Biological Trace Element Research, 2024, v. 202, n. 11, p. 4843, doi. 10.1007/s12011-023-04052-w
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- Article
Investigation of the Association of Serum Trace Elements Concentrations and Serum Biochemical Parameters with the Risk of Polycystic Ovary Syndrome: a Case–Control Study.
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- Biological Trace Element Research, 2024, v. 202, n. 1, p. 73, doi. 10.1007/s12011-023-03664-6
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Assessment of Serum Elements Concentration and Polycystic Ovary Syndrome (PCOS): Systematic Review and Meta-analysis.
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- Biological Trace Element Research, 2022, v. 200, n. 11, p. 4582, doi. 10.1007/s12011-021-03058-6
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- Article
Analysis of pro‐ and anti‐inflammatory cytokine gene variants and serum cytokine levels as prognostic markers in breast cancer.
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- Journal of Cellular Physiology, 2018, v. 233, n. 12, p. 9716, doi. 10.1002/jcp.26901
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- Article
Primordial dwarfism: overview of clinical and genetic aspects.
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- Molecular Genetics & Genomics, 2016, v. 291, n. 1, p. 1, doi. 10.1007/s00438-015-1110-y
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- Article
Meta‐analysis confirmed genetic susceptibility conferred by multiple risk variants from CTLA4 and SERPINA1 in granulomatosis with polyangiitis.
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- International Journal of Rheumatic Diseases, 2022, v. 25, n. 7, p. 811, doi. 10.1111/1756-185X.14354
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- Article
Genome-wide association study (GWAS) identified PCOS susceptibility variants and replicates reported risk variants.
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- Archives of Gynecology & Obstetrics, 2024, v. 309, n. 5, p. 2009, doi. 10.1007/s00404-024-07400-w
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- Article
Diagnostic and therapeutic approaches for endometriosis: a patent landscape.
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- Archives of Gynecology & Obstetrics, 2024, v. 309, n. 3, p. 831, doi. 10.1007/s00404-023-07151-0
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- Article
A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options.
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- Clinical Genetics, 2023, v. 103, n. 1, p. 16, doi. 10.1111/cge.14228
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- Article
Components of IGF-axis in growth disorders: a systematic review and patent landscape report.
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- Endocrine (1355008X), 2022, v. 76, n. 3, p. 509, doi. 10.1007/s12020-022-03063-2
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- Article
Functional implications of the CpG island methylation in the pathogenesis of celiac disease.
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- Molecular Biology Reports, 2022, v. 49, n. 10, p. 10051, doi. 10.1007/s11033-022-07585-w
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- Article
Clinical and Molecular Heterogeneity of Silver-Russell Syndrome and Therapeutic Challenges: A Systematic Review.
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- Current Pediatric Reviews, 2023, v. 19, n. 2, p. 157, doi. 10.2174/1573396318666220315142542
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- Article