Found: 19
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Steroidogenic acute regulatory protein (STAR) deficiency: Our experience and systematic review for phenotype–genotype correlation.
- Published in:
- Clinical Endocrinology, 2024, v. 100, n. 5, p. 431, doi. 10.1111/cen.15032
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- Article
Spontaneous Adrenal Hemorrhage in a Pregnant Woman With Glucocorticoid Resistance Syndrome.
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- JCEM Case Reports, 2024, v. 2, n. 4, p. 1, doi. 10.1210/jcemcr/luae052
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- Article
Inherited Fanconi renotubular syndromes: unveiling the intricacies of hypophosphatemic rickets/osteomalacia.
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- Journal of Bone & Mineral Metabolism, 2024, v. 42, n. 2, p. 155, doi. 10.1007/s00774-023-01490-3
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- Article
Overnight 1-mg DST Serum Cortisol in Various Stages of Chronic Kidney Disease—Normative Data and Underlying Mechanisms.
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- Journal of the Endocrine Society, 2024, v. 8, n. 3, p. 1, doi. 10.1210/jendso/bvae002
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- 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
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- Article
Pediatric Macrocorticotropinoma: Do They Differ from Microcorticotropinoma?
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- Neuroendocrinology, 2024, v. 114, n. 1, p. 42, doi. 10.1159/000533770
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- Article
Paediatric and adolescent ectopic Cushing’s syndrome: systematic review.
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- European Journal of Endocrinology, 2023, v. 189, n. 4, p. S75, doi. 10.1093/ejendo/lvad133
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- Article
Gonadotropin-Dependent Precocious Puberty: Single-Center Experience From Western India.
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- Indian Pediatrics, 2023, v. 60, n. 6, p. 463, doi. 10.1007/s13312-023-2909-y
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- Article
Genotypic Spectrum and its Correlation with Alopecia and Clinical Response in Hereditary Vitamin D Resistant Rickets: Our Experience and Systematic Review.
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- Calcified Tissue International, 2023, v. 112, n. 4, p. 483, doi. 10.1007/s00223-023-01061-8
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- Article
Abstract 137: Case series and systematic review of hormonal profile in genetically proven 46XX DSD with aromatase deficiency.
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- Indian Journal of Endocrinology & Metabolism, 2022, v. 26, p. 58, doi. 10.4103/2230-8210.363641
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- Article
Abstract 140: Pediatric macrocorticotropinoma: Do they differ from microcorticotropinoma?
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- Indian Journal of Endocrinology & Metabolism, 2022, v. 26, p. 60, doi. 10.4103/2230-8210.363644
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- Article
Abstract 147: Dual-phase computed tomography for localization of parathyroid lesions in adolescents with primary hyperparathyroidism.
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- Indian Journal of Endocrinology & Metabolism, 2022, v. 26, p. 63, doi. 10.4103/2230-8210.363651
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- Article
Genetic spectrum of Kallmann syndrome: Single‐center experience and systematic review.
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- Clinical Endocrinology, 2022, v. 97, n. 6, p. 804, doi. 10.1111/cen.14822
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- Article
Giant prolactinoma in children and adolescents: a single-center experience and systematic review.
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- Pituitary, 2022, v. 25, n. 6, p. 819, doi. 10.1007/s11102-022-01250-y
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- Article
Genotype-Phenotype Correlations in Asian Indian Children and Adolescents with Primary Hyperparathyroidism.
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- Calcified Tissue International, 2022, v. 111, n. 3, p. 229, doi. 10.1007/s00223-022-00985-x
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- Article
Pituitary stalk interruption syndrome: phenotype, predictors, and pathophysiology of perinatal events.
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- Pituitary, 2022, v. 25, n. 4, p. 645, doi. 10.1007/s11102-022-01243-x
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- Article
17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature.
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- Journal of the Endocrine Society, 2022, v. 6, n. 3, p. 1, doi. 10.1210/jendso/bvac011
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- Article
Role of preoperative blockade in pheochromocytoma–paraganglioma: A clinician's perspective.
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- Indian Journal of Endocrinology & Metabolism, 2022, v. 26, n. 1, p. 30, doi. 10.4103/2230-8210.343877
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- Article
Expanding genetic spectrum and discriminatory role of steroid profiling by LC‐MS/MS in 11β‐hydroxylase deficiency.
- Published in:
- Clinical Endocrinology, 2021, v. 94, n. 4, p. 533, doi. 10.1111/cen.14376
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- Article