Found: 12
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Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life.
- Published in:
- Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0287-9
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- Publication type:
- Article
Anti-Müllerian Hormone and Ovarian Morphology in Women With Isolated Hypogonadotropic Hypogonadism/Kallmann Syndrome: Effects of Recombinant Human FSH.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2017, v. 102, n. 4, p. 1102, doi. 10.1210/jc.2016-3799
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- Publication type:
- Article
Anti-Müllerian Hormone and Ovarian Morphology in Women With Isolated Hypogonadotropic Hypogonadism/Kallmann Syndrome: Effects of Recombinant Human FSH.
- Published in:
- 2017
- By:
- Publication type:
- journal article
New NOBOX Mutations Identified in a Large Cohort of Women With Primary Ovarian Insufficiency Decrease KIT-L Expression.
- Published in:
- 2015
- By:
- Publication type:
- Journal Article
Insulin-like Peptide 3 (INSL3) in Men With Congenital Hypogonadotropic Hypogonadism/Kallmann Syndrome and Effects of Different Modalities of Hormonal Treatment: A Single-Center Study of 281 Patients.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Kallmann’s Syndrome: A Comparison of the Reproductive Phenotypes in Men Carrying KAL1 and FGFR1/KAL2 Mutations.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 3, p. 758, doi. 10.1210/jc.2007-1168
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- Publication type:
- Article
Ovarian macrocysts and gonadotrope-ovarian axis disruption in premenopausal women receiving mitotane for adrenocortical carcinoma or Cushing's disease.
- Published in:
- European Journal of Endocrinology, 2015, v. 172, n. 2, p. 141, doi. 10.1530/EJE-14-0670
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- Publication type:
- Article
Prise en charge de l'infertilité des déficits gonadotropes chez la femme.
- Published in:
- Médecine de la Reproduction, 2023, v. 25, n. 3, p. 270, doi. 10.1684/mte.2023.0972
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- Publication type:
- Article
Cortisol and Aldosterone Responses to Hypoglycemia and Na Depletion in Women With Non-Classic 21-Hydroxylase Deficiency.
- Published in:
- 2019
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- Publication type:
- journal article
Testicular histological and immunohistochemical aspects in a post-pubertal patient with 5 alpha-reductase type 2 deficiency: case report and review of the literature in a perspective of evaluation of potential fertility of these patients.
- Published in:
- BMC Endocrine Disorders, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1472-6823-14-43
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- Publication type:
- Article
Secondary amenorrhoea associated with high serum 17-hydroxyprogesterone levels revealing a heterozygous CYP21A2 mutation in a woman with Addison disease.
- Published in:
- Clinical Endocrinology, 2015, v. 82, n. 4, p. 620, doi. 10.1111/cen.12646
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- Publication type:
- Article
Healthy birth after testicular extraction of sperm and ICSI from an azoospermic man with mild androgen insensitivity syndrome caused by an androgen receptor partial loss-of-function mutation.
- Published in:
- Clinical Endocrinology, 2012, v. 77, n. 4, p. 593, doi. 10.1111/j.1365-2265.2012.04402.x
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- Publication type:
- Article