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.
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
6.
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
7.
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
8.
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
9.
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
10.
Early Pulse Glucocorticoid Therapy and Improved Hormonal Outcomes in Primary Hypophysitis.
Neuroendocrinology
; 112(2): 186-195, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-33744880
11.
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
12.
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
13.
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
14.
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
15.
Pituitary stalk interruption syndrome: phenotype, predictors, and pathophysiology of perinatal events.
Pituitary
; 25(4): 645-652, 2022 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-35749012
16.
Exendin-4-based imaging in insulinoma localization: Systematic review and meta-analysis.
Clin Endocrinol (Oxf)
; 95(2): 354-364, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-33386617
17.
Expanding genetic spectrum and discriminatory role of steroid profiling by LC-MS/MS in 11ß-hydroxylase deficiency.
Clin Endocrinol (Oxf)
; 94(4): 533-543, 2021 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33275286
18.
Octreotide-LAR is a Useful Alternative for the Management of Diazoxide-Responsive Congenital Hyperinsulinism.
Horm Metab Res
; 53(11): 723-729, 2021 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-34740273
19.
Demographic and clinical profile of youth onset diabetes patients in India-Results from the baseline data of a clinic based registry of people with diabetes in India with young age at onset-[YDR-02].
Pediatr Diabetes
; 22(1): 15-21, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31885113
20.
POU1F1 mutations in combined pituitary hormone deficiency: differing spectrum of mutations in a Western-Indian cohort and systematic analysis of world literature.
Pituitary
; 24(5): 657-669, 2021 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-33742319