Detalhe da pesquisa
1.
A Rare Differences of Sex Development: Male Sex Reversal Syndrome (NonSyndromic 46, XX with Negative Sex-Determining Region of Y Chromosome Gene).
J Indian Assoc Pediatr Surg
; 28(2): 154-159, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37197249
2.
Indian Expert Review on Use of Teneligliptin in patients with Diabetes and its Safety and Efficacy (INTENSE).
J Assoc Physicians India
; 69(1): 61-70, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34227778
3.
DETERIORARON OF OVARIAN FUNCTION AFTER TOTAL ABDOMINAL HYSTERECTOMY WITH PRESERVARON OF OVARIES.
Endocr Pract
; 22(12): 1387-1392, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27540878
4.
Heterophilic Interference of Rheumatoid Factor in TSH Immunometric Assay: A Cross-Sectional Observational Study.
Indian J Endocrinol Metab
; 28(1): 29-34, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38533277
5.
Serum BAFF (B-cell activating factor) and APRIL (a proliferation-inducing ligand) levels in the first trimester may predict the future development of gestational diabetes mellitus.
Diabetes Metab Syndr
; 18(4): 103019, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38653036
6.
Toe brachial index and not ankle brachial index is appropriate in initial evaluation of peripheral arterial disease in type 2 diabetes.
Diabetol Metab Syndr
; 16(1): 52, 2024 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38414018
7.
Etiology and Biochemical Profile of Rickets in Tertiary Care Centres in Eastern India: A Retrospective Cross-sectional Study.
Indian J Endocrinol Metab
; 28(2): 184-191, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38911108
8.
Renal Dysfunction in Primary Hyperparathyroidism is associated with nephrolithiasis, elevated serum calcium-phosphate product and parathormone levels.
Endocrine
; 83(3): 757-762, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38091198
9.
Diabetic striatopathy and other acute onset de novo movement disorders in hyperglycemia.
Diabetes Metab Syndr
; 18(3): 102997, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38582065
10.
Split hand/foot malformation: a potential clue to underlying FGFR1 mutation in patients with isolated congenital hypogonadotropic hypogonadism.
Postgrad Med J
; 94(1109): 180-181, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29146774
11.
Addison's disease presenting with muscle spasm.
J Assoc Physicians India
; 61(9): 675-6, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24772716
12.
Marked increase in bone mineral density with oral phosphate and calcitriol in tumour-induced osteomalacia.
BMJ Case Rep
; 16(12)2023 Dec 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38056928
13.
The Real DAPSI: A Real-World Retrospective Study on Assessing the Efficacy and Safety of a Fixed-Dose Combination of Dapagliflozin and Sitagliptin in the Indian Population.
Cureus
; 15(10): e46767, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37954782
14.
Hypercalcemia in an Infant with Primary Hyperoxaluria Type 2: A Novel Association.
Indian J Nephrol
; 33(5): 387-391, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37881736
15.
Rickets in proximal renal tubular acidosis: a case series of six distinct etiologies.
J Pediatr Endocrinol Metab
; 36(9): 879-885, 2023 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37434360
16.
Diagnostic approach in 46, XY DSD: an endocrine society of bengal (ESB) consensus statement.
J Pediatr Endocrinol Metab
; 36(1): 4-18, 2023 Jan 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-36424806
17.
Pseudoacromegaly: an unusual presenting manifestation of long-standing undiagnosed primary hypothyroidism.
Postgrad Med J
; 93(1104): 639-640, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28500245
18.
Nonobese, Nonketotic Childhood-Onset Diabetes: Look for Lipodystrophies.
Clin Diabetes
; 35(4): 257-261, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29109619
19.
Leydig Cell Tumor-Induced Gonadotropin-Independent Precocious Puberty Progressing to Gonadotropin-Dependent Precocious Puberty Post Orchiectomy: Out of the Frying Pan Into the Fire.
Cureus
; 14(1): e21165, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-35165615
20.
Glial Cell Missing Homolog 2 Mutation Causing Severe Hypoparathyroidism: Report of Two Cases With Novel Mutations.
J Endocr Soc
; 7(1): bvac166, 2022 Nov 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36405867