V Chawla
This is a likely match — the affiliation was inferred from OpenAlex, ORCID, and web sources but has not been fully confirmed. Treat with appropriate caution.
Researcher
Graduate Student Researcher
Research Areas
Biography and Research Information
OverviewAI-generated summary
V Chawla's research focuses on medical case studies, particularly rare and complex presentations of diseases in neonates and individuals with genetic predispositions. Recent publications include a case report on severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21, highlighting the fatal presentation and therapeutic challenges. Another publication details a case of severe ascites in individuals with co-occurring Beckwith-Wiedemann and Li-Fraumeni syndromes, underscoring the collision of cancer predisposition syndromes. Chawla's work involves collaboration with researchers at the University of Arkansas for Medical Sciences, including JM Mack, Rachel Mayo, C Drummond, and D Becton.
Metrics
- Publications: 2
Selected Publications
-
Severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21: a rare, fatal presentation with complex therapeutic challenges (2026)
Collaboration Network
Top Collaborators
- Severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21: a rare, fatal presentation with complex therapeutic challenges
- Severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21: a rare, fatal presentation with complex therapeutic challenges
- Severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21: a rare, fatal presentation with complex therapeutic challenges
- Severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21: a rare, fatal presentation with complex therapeutic challenges
- Severe transient abnormal myelopoiesis in a premature neonate with Trisomy 21: a rare, fatal presentation with complex therapeutic challenges
Similar Researchers
Based on overlapping research topics