Found: 19
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Predictors of Chronic LH-Testosterone Axis Suppression in Male Macroprolactinomas With Normoprolactinemia on Cabergoline.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Pediatric Macrocorticotropinoma: Do They Differ from Microcorticotropinoma?
- Published in:
- Neuroendocrinology, 2024, v. 114, n. 1, p. 42, doi. 10.1159/000533770
- By:
- Publication type:
- Article
GNRH1 Variants in Congenital Hypogonadotropic Hypogonadism: Single-Center Experience and Systematic Literature Review.
- Published in:
- Neuroendocrinology, 2022, v. 112, n. 8, p. 723, doi. 10.1159/000521558
- By:
- Publication type:
- Article
Early Pulse Glucocorticoid Therapy and Improved Hormonal Outcomes in Primary Hypophysitis.
- Published in:
- Neuroendocrinology, 2022, v. 112, n. 2, p. 186, doi. 10.1159/000516006
- By:
- Publication type:
- Article
Renal manifestations of primary hyperparathyroidism.
- Published in:
- Indian Journal of Endocrinology & Metabolism, 2012, v. 16, n. 2, p. 258, doi. 10.4103/2230-8210.93745
- By:
- Publication type:
- Article
Pituitary apoplexy: a comprehensive analysis of 93 cases across functioning and non-functioning pituitary adenomas from a single-center.
- Published in:
- Pituitary, 2024, v. 27, n. 5, p. 705, doi. 10.1007/s11102-024-01453-5
- By:
- Publication type:
- Article
Pituitary apoplexy in cushing's disease: a single center study and systematic literature review.
- Published in:
- Pituitary, 2024, v. 27, n. 4, p. 335, doi. 10.1007/s11102-024-01411-1
- By:
- Publication type:
- Article
Giant prolactinoma in children and adolescents: a single-center experience and systematic review.
- Published in:
- Pituitary, 2022, v. 25, n. 6, p. 819, doi. 10.1007/s11102-022-01250-y
- By:
- Publication type:
- Article
Pituitary stalk interruption syndrome: phenotype, predictors, and pathophysiology of perinatal events.
- Published in:
- Pituitary, 2022, v. 25, n. 4, p. 645, doi. 10.1007/s11102-022-01243-x
- By:
- Publication type:
- Article
Regional genotypic variations in normosmic congenital hypogonadotropic hypogonadism: our experience and systematic review.
- Published in:
- Pituitary, 2022, v. 25, n. 3, p. 444, doi. 10.1007/s11102-022-01209-z
- By:
- Publication type:
- Article
17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature.
- Published in:
- Journal of the Endocrine Society, 2022, v. 6, n. 3, p. 1, doi. 10.1210/jendso/bvac011
- By:
- Publication type:
- Article
Clinical, Hormonal, Genetic, and Molecular Characteristics in Androgen Insensitivity Syndrome in an Asian Indian Cohort from a Single Centre in Western India.
- Published in:
- Sexual Development, 2021, v. 15, n. 4, p. 253, doi. 10.1159/000517763
- By:
- Publication type:
- Article
Paediatric and adolescent ectopic Cushing’s syndrome: systematic review.
- Published in:
- European Journal of Endocrinology, 2023, v. 189, n. 4, p. S75, doi. 10.1093/ejendo/lvad133
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- Publication type:
- Article
Homozygous p.Val89Leu plays an important pathogenic role in 5α-reductase type 2 deficiency patients with homozygous p.Arg246Gln in SRD5A2.
- Published in:
- European Journal of Endocrinology, 2020, v. 183, n. 3, p. 275, doi. 10.1530/EJE-19-1050
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- Publication type:
- Article
Luteinizing hormone β‐subunit deficiency: Report of a novel LHB likely pathogenic variant and a systematic review of the published literature.
- Published in:
- Clinical Endocrinology, 2023, v. 98, n. 3, p. 383, doi. 10.1111/cen.14749
- By:
- Publication type:
- Article
Inherited Fanconi renotubular syndromes: unveiling the intricacies of hypophosphatemic rickets/osteomalacia.
- Published in:
- Journal of Bone & Mineral Metabolism, 2024, v. 42, n. 2, p. 155, doi. 10.1007/s00774-023-01490-3
- By:
- Publication type:
- Article
Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review.
- Published in:
- Calcified Tissue International, 2024, v. 114, n. 2, p. 137, doi. 10.1007/s00223-023-01156-2
- By:
- Publication type:
- Article
Genotypic Spectrum and its Correlation with Alopecia and Clinical Response in Hereditary Vitamin D Resistant Rickets: Our Experience and Systematic Review.
- Published in:
- Calcified Tissue International, 2023, v. 112, n. 4, p. 483, doi. 10.1007/s00223-023-01061-8
- By:
- Publication type:
- Article
Genetic spectrum of Kallmann syndrome: Single‐center experience and systematic review.
- Published in:
- Clinical Endocrinology, 2022, v. 97, n. 6, p. 804, doi. 10.1111/cen.14822
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- Publication type:
- Article