Hiren Panwala

ORCID: 0000-0003-3718-8708
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About
Contact & Profiles
Research Areas
  • Long-Term Effects of COVID-19
  • Liver Disease and Transplantation
  • Lysosomal Storage Disorders Research
  • Glioma Diagnosis and Treatment
  • Ocular Diseases and Behçet’s Syndrome
  • Extracellular vesicles in disease
  • Liver Disease Diagnosis and Treatment
  • COVID-19 Clinical Research Studies
  • RNA regulation and disease
  • Fungal Infections and Studies
  • Parkinson's Disease Mechanisms and Treatments
  • Vascular anomalies and interventions
  • Abdominal vascular conditions and treatments
  • Congenital Diaphragmatic Hernia Studies
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Neuroblastoma Research and Treatments
  • Cytomegalovirus and herpesvirus research
  • Osteomyelitis and Bone Disorders Research
  • Vascular Malformations and Hemangiomas
  • Retinal and Optic Conditions
  • Inflammasome and immune disorders
  • Tumors and Oncological Cases
  • Urologic and reproductive health conditions
  • interferon and immune responses

SRCC Children’s Hospital
2020-2023

Narayana Health
2022

Creative Commons
2022

Christian Medical College
2018-2019

Christian Medical College & Hospital
2018-2019

Krabbe disease shows considerable heterogeneity in clinical features and progression. Imaging phenotypes are equally heterogeneous but show distinct age-based patterns. It is important for radiologists to be familiar with the imaging spectrum substantially contribute toward early diagnosis, prognostication, therapeutic decisions.The study aims describe different magnetic resonance (MRI) patterns observed a cohort of children assess correlation phenotypes.This retrospective descriptive done...

10.25259/jcis-18-2019 article EN Journal of Clinical Imaging Science 2019-05-24

Introduction: We present one of the largest case series Macrodystrophia lipomatosa, a rare congenital disorder localized gigantism characterized by overgrowth all mesenchymal elements, predominantly involving fibroadipose tissue. Aims: To detail radiological features, pattern distribution, associated conditions and to suggest an appropriate terminology describe condition. Methods Material: It is retrospective study. Data from PACS server dating 2000 2018 was used. The cases with isolated...

10.25259/jcis-9-4 article EN cc-by-nc-sa Journal of Clinical Imaging Science 2019-02-27

Aim: The aim of our study was to evaluate the computed tomography (CT) imaging features splenic artery aneurysm and pseudoaneurysm identify disease conditions related same. We also wanted ascertain any relationship between these associated aneurysms. Materials Methods: This retrospective included patients diagnosed have aneurysms on contrast-enhanced CT examination January 2001 2016. Data were obtained from picture archiving communication system. size, number, location, morphology, presence...

10.4103/jcis.jcis_21_18 article EN cc-by-nc-sa Journal of Clinical Imaging Science 2018-08-24

Abstract Paediatric extra-cranial solid tumours are one of the common causes for paediatric malignancies. Lack appropriate imaging at presentation, staging and follow-up is a major challenge tumours. We have reviewed tumour protocols suggested by oncological societies/groups around world (mainly SIOP – Society International Pediatric Oncology, COG Children's Oncology Group). adapted some those to develop recommendations diagnosis, management based on treatment followed in India.

10.1055/s-0042-1759507 article EN cc-by Indian Journal of Medical and Paediatric Oncology 2023-02-01

Abstract Optic Neuritis is the most common presentation of MOG Antibody Disease (MOG-AD). We share our experience with a 11-year-old boy who developed associated temporally SARS- CoV-2 infection. He responded well to intravenous methylprednisolone therapy followed by oral prednisolone. While various neurological and ophthalmological manifestations COVID-19 have been described previously, there are few case reports neuritis COVID-19. Our further supports evidence suggest that SARS another...

10.21203/rs.3.rs-104308/v1 preprint EN cc-by Research Square (Research Square) 2020-11-10

Background: Krabbe's disease is a neurodegenerative condition caused by deficiency of lysosomal enzyme, galactocerebrosidase (GALC), found mainly in the brain. There are four variants based on age onset: Infantile, late infantile, juvenile, and adult. Hematopoietic stem cell transplants can be curative as GALC-positive donor cells migrate to brain provide GALC, thus correcting deficiency. However, this most effective when performed asymptomatic or mildly symptomatic phase. Maximum experience...

10.4103/ipcares.ipcares_94_22 article EN cc-by-nc-sa Indian Pediatrics Case Reports 2022-07-01
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