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Efficacy and safety of burosumab compared with conventional therapy in patients with X-linked hypophosphatemia: A systematic review

Archives of Endocrinology and Metabolism, 2024-05, Vol.68, p.e230242

2024

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177Lu-DOTATATE therapy in metastatic/inoperable pheochromocytoma-paraganglioma

Endocrine Connections, 2020-09, Vol.9 (9), p.864-873

2020

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Predictors of Chronic LH-Testosterone Axis Suppression in Male Macroprolactinomas With Normoprolactinemia on Cabergoline

The journal of clinical endocrinology and metabolism, 2020-12, Vol.105 (12), p.1-e4557

2020

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Metastatic cluster 2-related pheochromocytoma/paraganglioma: a single-center experience and systematic review

Endocrine Connections, 2021-11, Vol.10 (11), p.1463-1476

2021

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Vitamin D deficiency or resistance and hypophosphatemia

Best Practice & Research Clinical Endocrinology & Metabolism, 2024-03, Vol.38 (2), p.101876-101876, Article 101876

2024

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Pediatric Macrocorticotropinoma: Do They Differ from Microcorticotropinoma?

Neuroendocrinology, 2024, Vol.114 (1), p.42

2024

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Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review

Calcified tissue international, 2024-02, Vol.114 (2), p.137-146

2024

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Early Pulse Glucocorticoid Therapy and Improved Hormonal Outcomes in Primary Hypophysitis

Neuroendocrinology, 2022-02, Vol.112 (2), p.186-195

2022

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Luteinizing hormone β‐subunit deficiency: Report of a novel LHB likely pathogenic variant and a systematic review of the published literature

Clinical endocrinology (Oxford), 2023-03, Vol.98 (3), p.383-393

2023

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Genotypic Spectrum and its Correlation with Alopecia and Clinical Response in Hereditary Vitamin D Resistant Rickets: Our Experience and Systematic Review

Calcified tissue international, 2023-04, Vol.112 (4), p.483-492

2023

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Pituitary stalk interruption syndrome: phenotype, predictors, and pathophysiology of perinatal events

Pituitary, 2022-08, Vol.25 (4), p.645-652

2022

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Genetic spectrum of Kallmann syndrome: Single‐center experience and systematic review

Clinical endocrinology (Oxford), 2022-12, Vol.97 (6), p.804-813

2022

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Giant prolactinoma in children and adolescents: a single-center experience and systematic review

Pituitary, 2022-12, Vol.25 (6), p.819-830

2022

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Diagnostic performance of various imaging modalities in localizing Ectopic ACTH syndrome: A Systematic review

Annales d'endocrinologie, 2024-07

2024

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Inherited Fanconi renotubular syndromes: unveiling the intricacies of hypophosphatemic rickets/osteomalacia

Journal of bone and mineral metabolism, 2024-03, Vol.42 (2), p.155-165

2024

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Pituitary apoplexy in cushing’s disease: a single center study and systematic literature review

Pituitary, 2024-06

2024

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GNRH1 Variants in Congenital Hypogonadotropic Hypogonadism: Single-Center Experience and Systematic Literature Review

Neuroendocrinology, 2022-08, Vol.112 (8), p.723-732

2022

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Giant prolactinoma in Asian-Indians: A single-center experience from Western India

Annales d'endocrinologie, 2023-12, Vol.84 (6), p.711-718

2023

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Renal manifestations of primary hyperparathyroidism

Indian journal of endocrinology and metabolism, 2012-03, Vol.16 (2), p.258-262

2012

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46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters

Annales d'endocrinologie, 2024-02, Vol.85 (1), p.48-55

2024

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Regional genotypic variations in normosmic congenital hypogonadotropic hypogonadism: our experience and systematic review

Pituitary, 2022-06, Vol.25 (3), p.444-453

2022

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Clinical, Hormonal, Genetic, and Molecular Characteristics in Androgen Insensitivity Syndrome in an Asian Indian Cohort from a Single Centre in Western India

Sexual development, 2021-09, Vol.15 (4), p.253-261

2021

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17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature

Journal of the Endocrine Society, 2022-03, Vol.6 (3), p.bvac011-bvac011

2022

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17[alpha]-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature

Journal of the Endocrine Society, 2022-03, Vol.6 (3)

2022

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Posterior Reversible Encephalopathy Syndrome due to Ectopic Cushing’s Syndrome: An Uncommon Presentation of a Rare Disease

Indian journal of pediatrics, 2015-03, Vol.82 (3), p.294-295

2015

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Efficacy and safety of burosumab compared with conventional therapy in patients with X-linked hypophosphatemia: A systematic review

177Lu-DOTATATE therapy in metastatic/inoperable pheochromocytoma-paraganglioma

Predictors of Chronic LH-Testosterone Axis Suppression in Male Macroprolactinomas With Normoprolactinemia on Cabergoline

Metastatic cluster 2-related pheochromocytoma/paraganglioma: a single-center experience and systematic review

Vitamin D deficiency or resistance and hypophosphatemia

Pediatric Macrocorticotropinoma: Do They Differ from Microcorticotropinoma?

Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review

Early Pulse Glucocorticoid Therapy and Improved Hormonal Outcomes in Primary Hypophysitis

Luteinizing hormone β‐subunit deficiency: Report of a novel LHB likely pathogenic variant and a systematic review of the published literature

Genotypic Spectrum and its Correlation with Alopecia and Clinical Response in Hereditary Vitamin D Resistant Rickets: Our Experience and Systematic Review

Pituitary stalk interruption syndrome: phenotype, predictors, and pathophysiology of perinatal events

Genetic spectrum of Kallmann syndrome: Single‐center experience and systematic review

Giant prolactinoma in children and adolescents: a single-center experience and systematic review

Diagnostic performance of various imaging modalities in localizing Ectopic ACTH syndrome: A Systematic review

Inherited Fanconi renotubular syndromes: unveiling the intricacies of hypophosphatemic rickets/osteomalacia

Pituitary apoplexy in cushing’s disease: a single center study and systematic literature review

GNRH1 Variants in Congenital Hypogonadotropic Hypogonadism: Single-Center Experience and Systematic Literature Review

Giant prolactinoma in Asian-Indians: A single-center experience from Western India

Renal manifestations of primary hyperparathyroidism

46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters

Regional genotypic variations in normosmic congenital hypogonadotropic hypogonadism: our experience and systematic review

Clinical, Hormonal, Genetic, and Molecular Characteristics in Androgen Insensitivity Syndrome in an Asian Indian Cohort from a Single Centre in Western India

17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature

17[alpha]-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature

Posterior Reversible Encephalopathy Syndrome due to Ectopic Cushing’s Syndrome: An Uncommon Presentation of a Rare Disease

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