Detalhe da pesquisa
1.
Beyond the Four Walls: The American College of Emergency Physicians 2022 New Practice Models Task Force Report.
Ann Emerg Med
; 83(3): 250-271, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37777937
2.
Genotype-phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India.
Neurogenetics
; 24(1): 43-53, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36580222
3.
Variants in complement genes are uncommon in patients with anti-factor H autoantibody-associated atypical hemolytic uremic syndrome.
Pediatr Nephrol
; 38(8): 2659-2668, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36622444
4.
Applications, benefits and challenges of telehealth in India during COVID-19 pandemic and beyond: a systematic review.
BMC Health Serv Res
; 23(1): 7, 2023 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36597088
5.
RAGE antagonism with azeliragon improves xenograft rejection by T cells in humanized mice.
Clin Immunol
; 245: 109165, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36257528
6.
Efficacy of emicizumab in von Willebrand disease (VWD) patients with and without alloantibodies to von Willebrand factor (VWF): Report of two cases and review of literature.
Haemophilia
; 28(2): 286-291, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35014121
7.
Next Generation Sequencing and Cytogenetic Based Evaluation of Indian Pierre Robin Sequence Families Reveals CNV Regions of Modest Effect and a Novel LOXL3 Mutation.
Cleft Palate Craniofac J
; 59(11): 1329-1339, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34787502
8.
National Estimates of Workplace Telehealth Use Among Emergency Nurses and All Registered Nurses in the United States.
J Emerg Nurs
; 48(1): 45-56, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34656361
9.
A founder mutation in the GMPPB gene [c.1000G > A (p.Asp334Asn)] causes a mild form of limb-girdle muscular dystrophy/congenital myasthenic syndrome (LGMD/CMS) in South Indian patients.
Neurogenetics
; 22(4): 271-285, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34333724
10.
An Indian child with Coats plus syndrome due to mutations in STN1.
Am J Med Genet A
; 182(9): 2139-2144, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32627942
11.
Telehealth in the time of COVID-19.
Emerg Med J
; 37(10): 637-638, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32753392
12.
Hospital Telehealth Adoption Increased in 2014 and 2015 and Was Influenced by Population, Hospital, and Policy Characteristics.
Telemed J E Health
; 26(4): 455-461, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31120388
13.
Whole exome and targeted gene sequencing to detect pathogenic recessive variants in early onset cerebellar ataxia.
Clin Genet
; 96(6): 566-574, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31429931
14.
Prevalence of FVIII inhibitors in severe haemophilia A patients: Effect of treatment and genetic factors in an Indian population.
Haemophilia
; 25(1): 67-74, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30427567
15.
A novel mutation in SLC39A14 causing hypermanganesemia associated with infantile onset dystonia.
J Gene Med
; 20(4): e3012, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29498153
16.
Accessory Cavitated Uterine Mass: An Emerging Differential Diagnosis of Dysmenorrhea in Adolescents.
J Minim Invasive Gynecol
; 28(6): 1131-1132, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33359290
17.
A Rare Case of Intravascular Fibroid Incidentally Diagnosed Intraoperatively.
J Minim Invasive Gynecol
; 28(12): 1971-1972, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34469827
18.
Obstructed Hemivagina and Ipsilateral Renal Anomaly Syndrome: A Rare Müllerian Abnormality.
J Minim Invasive Gynecol
; 27(7): 1457-1460, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32142891
19.
Laparoscopic Port Site Dermoid Cyst: A Rare and Unusual Presentation.
J Minim Invasive Gynecol
; 27(7): 1455-1456, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32135245
20.
Comparison of EPDS Scores Among Women with Good Neonatal Outcomes and Adverse Neonatal Outcomes.
J Obstet Gynaecol India
; 73(6): 552-554, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38205111