- Prenatal Screening and Diagnostics
- Urological Disorders and Treatments
- Congenital Anomalies and Fetal Surgery
- Ethics and Legal Issues in Pediatric Healthcare
- Congenital gastrointestinal and neural anomalies
- Vascular anomalies and interventions
- Congenital Diaphragmatic Hernia Studies
- Autopsy Techniques and Outcomes
- Cardiac Ischemia and Reperfusion
- Anesthesia and Neurotoxicity Research
- Vascular Malformations and Hemangiomas
- Coronary Artery Anomalies
- Teratomas and Epidermoid Cysts
- Parvovirus B19 Infection Studies
- Biomedical Research and Pathophysiology
- Pediatric Urology and Nephrology Studies
- Cardiac Structural Anomalies and Repair
- Congenital Heart Disease Studies
- Renal and related cancers
- Fetal and Pediatric Neurological Disorders
- Traumatic Brain Injury and Neurovascular Disturbances
- Neonatal and fetal brain pathology
- Occupational exposure and asthma
- Tumors and Oncological Cases
- Coronary Interventions and Diagnostics
Jawaharlal Institute of Post Graduate Medical Education and Research
2015-2024
Mount Sinai Hospital
2024
Mandya Institute of Medical Sciences
2015-2022
Stamford Hospital
2021
Sanjay Gandhi Post Graduate Institute of Medical Sciences
2013
Wake Forest University
1995-1999
Atrium Health Wake Forest Baptist
1995-1997
Temporary elevations in cortical cerebral blood flow (CBF) accompany spreading depression (CSD) anesthetized animals. We tested the hypothesis that nitric oxide (NO) is an important promotor of CSD-induced hyperemia urethan-anesthetized rabbits. CBF was measured at four time points by administration 15-microm microspheres with reference withdrawal technique. Intravenous nonspecific NO synthase (NOS) inhibitor N(omega)-nitro-L-arginine increased mean arterial pressure and resting...
Coronary artery calcification (CAC) may provide insight to the patients' coronary disease (CAD) risks and influence early intervention. With increasing use of non-gated CT scans in clinical practice, visual scoring system (Weston Method) could quickly clinicians with important information CAC for patient triage management.
Congenital heart defects(CHDs) are an important cause of neonatal mortality and morbidity. With advances in diagnosis treatment, many defects now amenable to correction. There is a need for individualized approach prenatally detected lesions predict the likely prognosis. Assigning them into risk category helps prenatal counseling, decision making, referrals formulation management plan improve outcome.To grade fetal CHDs according severity study its usefulness making.A prospective at tertiary...
Aim: To describe the ultrasonographic appearance of fetal ventricular aneurysm.Methods: Ultrasound characteristics two cases prenatally diagnosed aneurysm were reviewed.Results: There was one case left by prenatal ultrasound at 38 weeks gestation. Another right 36 Both babies expired in immediate post-natal period.Conclusion: Congenital is a rare cardiac malformation characterized protrusion or out pouching portion wall. It important to differentiate an from diverticulum, as latter has...
Background: Knowledge of the normal and variant arterial anatomy upper extremity is significant clinical importance for vascular radiologist surgeons accurate diagnostic interpretation as well in conduct interventional surgical procedures on extremity. The anatomical knowledge anomalous branching pattern brachial artery important during percutaneous catheterization, so to prevent any complications arising from accidental damage vessel variations are plastic using flaps reconstructive...
Sirenomelia is a rare congenital disorder with complete or partial fusion of lower limbs. The incidence reported to vary from 0.01–0.16/10,000 live births male female ratio 3:1.1 Risk factors include maternal gestational diabetes mellitus, tobacco use, and retinoic acid heavy metal exposure. usually incompatible life due associated visceral anomalies. Here, we report case multiple anomalies in the VACTERL spectrum which suggest link pathogenesis between two conditions.
We present a case of silicosis in 37-year-old pregnant woman, second gravida with previous caesarean section. She was referred to our hospital at 42 weeks gestation breathlessness and oligohydramnios. had worked glass talc powder factory for 11 years diagnosed as having 2 prior; she on treatment. Following admission, evaluated dyspnoea underwent emergency Caesarean section poor cervical dilation. developed burst abdomen the third postoperative day loops gangrenous bowel protruding outside...
Abstract We report a case of germinal matrix intraventricular hemorrhage (GMIVH) diagnosed antenatally at 30 weeks gestation. The pregnancy was continued with close monitoring up to 37 A healthy baby delivered and had normal neurological development after 8 months postnatal follow-up. GMIVH, though common in premature neonates, is rarely seen fetal life. Diagnosis possible by prenatal ultrasound usually the third trimester. Tomographic imaging useful alternative MRI assessing extent...
ABSTRACT RNA polymerase III (Pol III, POLR3) synthesizes tRNAs and other small non-coding RNAs. Human POLR3 pathogenic variants cause a range of developmental disorders, recapitulated in part by mouse models, yet some aspects deficiency have not been explored. We characterized human POLR3B :c.1625A>G;p.(Asn542Ser) disease variant that was found to mis-splicing . Genome-edited 1625A>G HEK293 cells acquired the with decreases multiple subunits TFIIIB, although display auto-upregulation...
Yadav, Manisha; Gowda, Mamatha; Navya, Chinta; Deodhare, Kirti; Murugesan, Sneha Author Information
Background: Fetal cardiac rhythm disruptions pose significant challenges to prenatal and postnatal well-being. These disruptions, encompassing various arrhythmias, necessitate timely diagnosis precise management. Transabdominal fetal echocardiography has become a crucial diagnostic tool for evaluating enabling tailored interventions. Objectives: This retrospective study aims examine 40 cases of arrhythmias at our institution, shedding light on common abnormalities, intricacies, therapeutic...
To treat the fetus presenting with in utero compromise due to a large vein of Galen malformation (VOGM) using glue embolization.