Found: 10
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NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency.
- Published in:
- Clinical Genetics, 2016, v. 89, n. 5, p. 608, doi. 10.1111/cge.12750
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- Publication type:
- Article
PROKR2 variants in multiple hypopituitarism with pituitary stalk interruption.
- Published in:
- 2012
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- Publication type:
- Journal Article
Germline AIP mutations in apparently sporadic pituitary adenomas: prevalence in a prospective single-center cohort of 443 patients.
- Published in:
- 2012
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- Publication type:
- Journal Article
THE HYPOPHYSIOTROPIC NEUROPEPTIDE GnRH VALIDATED AS THE CONDUCTOR OF PUBERTY AND REPRODUCTION IN HUMANS.
- Published in:
- Acta Endocrinologica (1841-0987), 2010, v. 6, n. 3, p. 355, doi. 10.4183/aeb.2010.355
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- Publication type:
- Article
Effect of NFE2L2 Genetic Polymorphism on the Association Between Oral Estrogen Therapy and the Risk of Venous Thromboembolism in Postmenopausal Women.
- Published in:
- Clinical Pharmacology & Therapeutics, 2011, v. 89, n. 1, p. 60, doi. 10.1038/clpt.2010.241
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- Publication type:
- Article
Elevated Plasma Ferritin and Busulfan Pharmacodynamics During High-dose Chemotherapy Regimens in Children with Malignant Solid Tumors.
- Published in:
- Clinical Pharmacology & Therapeutics, 2007, v. 82, n. 4, p. 402, doi. 10.1038/sj.clpt.6100168
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- Publication type:
- Article
High‐throughput sequencing in prenatal care: how to combine diagnostic performance and best practice?
- Published in:
- Ultrasound in Obstetrics & Gynecology, 2024, v. 63, n. 5, p. 704, doi. 10.1002/uog.27652
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- Publication type:
- Article
Persistent Müllerian duct syndrome due to anti-Müllerian hormone receptor 2 microdeletions: a diagnostic challenge.
- Published in:
- 2020
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- Publication type:
- journal article
In children and adolescents, the pharmacodynamics of high-dose busulfan is dependent on the second alkylating agent used in the combined regimen (melphalan or thiotepa).
- Published in:
- Bone Marrow Transplantation, 2003, v. 32, n. 10, p. 979, doi. 10.1038/sj.bmt.1704275
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- Publication type:
- Article
Maralixibat-treated patients with Alagille syndrome (ALGS) demonstrate improved event-free survival in a natural history comparison with patients from the GALA database: application of real-world evidence analytics.
- Published in:
- Journal of Pediatric Gastroenterology & Nutrition, 2022, v. 74, p. 670, doi. 10.1097/MPG.0000000000003446
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- Publication type:
- Article