Detalhe da pesquisa
1.
Steroidogenic acute regulatory protein (STAR) deficiency: Our experience and systematic review for phenotype-genotype correlation.
Clin Endocrinol (Oxf)
; 100(5): 431-440, 2024 May.
Artigo
Inglês
| MEDLINE | ID: mdl-38368602
2.
Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review.
Calcif Tissue Int
; 114(2): 137-146, 2024 02.
Artigo
Inglês
| MEDLINE | ID: mdl-37981601
3.
Pediatric Macrocorticotropinoma: Do They Differ from Microcorticotropinoma?
Neuroendocrinology
; 114(1): 42-50, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-37634509
4.
Inherited Fanconi renotubular syndromes: unveiling the intricacies of hypophosphatemic rickets/osteomalacia.
J Bone Miner Metab
; 42(2): 155-165, 2024 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-38310177
5.
Update on Primary Aldosteronism: Time to Screen All Hypertensives.
J Assoc Physicians India
; 72(1): 11-12, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-38736067
6.
Luteinizing hormone ß-subunit deficiency: Report of a novel LHB likely pathogenic variant and a systematic review of the published literature.
Clin Endocrinol (Oxf)
; 98(3): 383-393, 2023 03.
Artigo
Inglês
| MEDLINE | ID: mdl-35470463
7.
Side-chain cleavage enzyme deficiency: Systematic review and case series.
Clin Endocrinol (Oxf)
; 98(3): 351-362, 2023 03.
Artigo
Inglês
| MEDLINE | ID: mdl-36357326
8.
Machine learning for predicting diabetic metabolism in the Indian population using polar metabolomic and lipidomic features.
Metabolomics
; 20(1): 1, 2023 Nov 28.
Artigo
Inglês
| MEDLINE | ID: mdl-38017183
9.
Genotypic Spectrum and its Correlation with Alopecia and Clinical Response in Hereditary Vitamin D Resistant Rickets: Our Experience and Systematic Review.
Calcif Tissue Int
; 112(4): 483-492, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36705686
10.
Prevalence of primary aldosteronism in type 2 diabetes mellitus and hypertension: A prospective study from Western India.
Clin Endocrinol (Oxf)
; 96(4): 539-548, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-34580897
11.
Genetic spectrum of Kallmann syndrome: Single-center experience and systematic review.
Clin Endocrinol (Oxf)
; 97(6): 804-813, 2022 12.
Artigo
Inglês
| MEDLINE | ID: mdl-36138264
12.
68 Ga-DOTATATE PET/CT imaging in endogenous hyperinsulinemic hypoglycemia: A tertiary endocrine centre experience.
Clin Endocrinol (Oxf)
; 96(2): 190-199, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34498757
13.
17ß hydroxysteroid dehydrogenase 3 deficiency in 46,XY disorders of sex development: Our experience and a gender role-focused systematic review.
Clin Endocrinol (Oxf)
; 97(1): 43-51, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35170787
14.
Genotype-Phenotype Correlations in Asian Indian Children and Adolescents with Primary Hyperparathyroidism.
Calcif Tissue Int
; 111(3): 229-241, 2022 09.
Artigo
Inglês
| MEDLINE | ID: mdl-35567607
15.
Early Pulse Glucocorticoid Therapy and Improved Hormonal Outcomes in Primary Hypophysitis.
Neuroendocrinology
; 112(2): 186-195, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-33744880
16.
GNRH1 Variants in Congenital Hypogonadotropic Hypogonadism: Single-Center Experience and Systematic Literature Review.
Neuroendocrinology
; 112(8): 723-732, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-34923491
17.
Clinical Spectrum of Adrenal Cushing's Syndrome and the Caution for Interpretation of Adrenocorticotrophic Hormone: A Single-Center Experience.
Horm Metab Res
; 54(2): 57-66, 2022 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-35130566
18.
Giant prolactinoma in children and adolescents: a single-center experience and systematic review.
Pituitary
; 25(6): 819-830, 2022 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-35851929
19.
Regional genotypic variations in normosmic congenital hypogonadotropic hypogonadism: our experience and systematic review.
Pituitary
; 25(3): 444-453, 2022 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-35133534
20.
Pituitary stalk interruption syndrome: phenotype, predictors, and pathophysiology of perinatal events.
Pituitary
; 25(4): 645-652, 2022 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-35749012