Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Parag Bhalgat"'
Publikováno v:
JACC: Case Reports, Vol 3, Iss 5, Pp 715-720 (2021)
Rare cardiac malpositions are faced with diagnostic challenges and may not follow set rules. The presence of more than one pathology simultaneously makes diagnosis challenging. The present case report describes antennal diagnosis topsy-turvy heart wi
Externí odkaz:
https://doaj.org/article/3e3fe2d4fa1540e9b704b31bd8aa576e
Publikováno v:
IHJ Cardiovascular Case Reports, Vol 4, Iss 2, Pp 68-71 (2020)
Ebstein anomaly is rare congenital heart defect and frequently associated with various other cardiac defects. Here we present a combination of Ebstein anomaly with supra cardiac total anomalous pulmonary venous drainage, ostium secundum atrial septal
Externí odkaz:
https://doaj.org/article/a991fb2300144da8b5bf30426bbd7f9a
Publikováno v:
IHJ Cardiovascular Case Reports, Vol 4, Iss 2, Pp 77-79 (2020)
Tetralogy of Fallot (TOF) in association with aorto pulmonary window (APW) is a very rare congenital cardiac defect. Only a handful of cases have been reported in world literature. Though TOF can be diagnosed with fair accuracy on echocardiography, A
Externí odkaz:
https://doaj.org/article/72ba7f0d98d34e72ae8b01146f4777e8
Autor:
Parag Bhalgat, Abhijeet Naik, Prasanna Salvi, Nilesh Bhadane, Kshiti Shah, Bhawan Paunipagar, Suresh Joshi
Publikováno v:
Indian Heart Journal, Vol 70, Iss 2, Pp 303-307 (2018)
Background: Anomalous origin of left coronary artery from pulmonary artery (ALCAPA) is a very rare congenital heart defect characterized by myocardial ischemia and ultimately scaring. The scar burden will determine eventual recovery of left ventricul
Externí odkaz:
https://doaj.org/article/de30daa1a352446db7de20229bc131d3
Autor:
Haribalakrishna Balasubramanian, Vaibhav Jain, Parag Bhalgat, Shalin Parikh, Nandkishore Kabra, Diwakar Mohan, Kshitij Sheth
Publikováno v:
Archives of Disease in Childhood - Fetal and Neonatal Edition. 108:130-135
ObjectiveTo compare the efficacy of low dose-short course intravenous paracetamol with a conventional dose regimen for early targeted closure of patent ductus arteriosus (PDA).DesignSingle-centre, double-blinded, active controlled, randomised non-inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::808e856454f8d3234955299a499aeb11
https://doi.org/10.1136/archdischild-2022-323781
https://doi.org/10.1136/archdischild-2022-323781
Autor:
Parag Bhalgat, Pooja Bhalgat
Publikováno v:
Journal of Fetal Medicine.
Management of fetal supraventricular tachycardia at times can be tricky and challenging when they are secondary to underlying metabolic or hormonal problems. It can difficult to unmask the real culprit unless thorough evaluation is performed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c0d4467c645f0daae0905a075afd0cd
https://doi.org/10.1055/s-0043-57023
https://doi.org/10.1055/s-0043-57023
Autor:
Parag Bhalgat, Shrivallabh Karlekar, Santosh Modani, Ashish Agrawal, Charan Lanjewar, Ashish Nabar, Prafulla Kerkar, Nandu Agrawal, Pradeep Vaideeswar
Publikováno v:
Indian Heart Journal, Vol 67, Iss 5, Pp 428-433 (2015)
Background: Balloon mitral valvotomy (BMV) is a well-established therapeutic modality for rheumatic mitral stenosis (RMS). However, there are chances of procedural failure and the more ominous post-procedural severe mitral regurgitation. There are on
Externí odkaz:
https://doaj.org/article/bc778de3e9ff43fb8689a628548fd4c2
Autor:
Bharat Dalvi, Parag Bhalgat
Publikováno v:
Circulation: Cardiovascular Interventions. 15
Background: Two separate ostium secundum atrial septal defects are a challenging substrate for device closure due to lack of a well-described strategy or an adequately evaluated protocol. Methods: This is a prospective study comprising 20 patients wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d97e051f8149f56be43c863650e41b9c
https://doi.org/10.1161/circinterventions.122.012048
https://doi.org/10.1161/circinterventions.122.012048
Publikováno v:
Clinical Cardiology and Cardiovascular Interventions. 4:01-04
The combination of aortic coarctation (CoA) and bicuspid aortic valve (BAV) is associated with high risk of ascending aortic dilatation and type A aortic dissection. Most of the patients having combined lesions remain asymptomatic until adulthood and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bee6c8b0cd68590466b24dc273e70fff
https://doi.org/10.31579/2641-0419/169
https://doi.org/10.31579/2641-0419/169
Autor:
Yogeshkumar Choudhary, Parag Bhalgat
Publikováno v:
Indian Journal of Obstetrics and Gynecology Research. 6:414-419
Congenital heart defects are leading cause of neonatal mortality even in developed world. It is result of either late diagnosis of defect after circulatory compromise or discharge of neonates with undiagnosed defect. Antenatal anomaly scan provides a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4fcf698cf2a5e68b6879abd3dcace83
https://doi.org/10.18231/j.ijogr.2019.092
https://doi.org/10.18231/j.ijogr.2019.092