Indrani Dhawan
Vardhman Mahavir Medical College
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Publication
Featured researches published by Indrani Dhawan.
American Journal of Reproductive Immunology | 2015
Gayatri Rath; Poonam Jawanjal; Sudha Salhan; Manoharan Nalliah; Indrani Dhawan
To determine the role of inactivated GSK3β with respect to Wnt/β‐catenin pathway activation in HPV‐16/18‐associated cervical cancer.
Journal of Clinical Laboratory Analysis | 2016
Poonam Jawanjal; Sudha Salhan; Indrani Dhawan; Nirmalendu Das; Ruby Aggarwal; Richa Tripathi; Gayatri Rath
Cyclooxygenase‐2 (Cox‐2) is frequently overexpressed in cervical carcinoma, but little is known about its altered serum concentration. Hence, this study evaluates clinical utility of cellular and serum level of Cox‐2 enzyme in cervical cancer.
Journal of Obstetrics and Gynaecology | 2018
Jyoti Rajpoot; Neelam Sahani; Sufian Zaheer; Indrani Dhawan
Gliomatosis peritonei, a rare benign condition, is defined as the presence of mature glial tissue on the peritoneum, omentum and abdominal lymph nodes. The disease was first described by Neuhauser ...
International journal of reproduction, contraception, obstetrics and gynecology | 2017
Gireesha Rawal; Sufian Zaheer; Amit Kumar Yadav; Neelam Sahani; Indrani Dhawan
The synchronous or metachronous occurrance of multiple primary cancers in the genital tract is well recognized. The overall incidence of synchronous female genital tract malignancies is 0.63%. The most frequently observed synchronous neoplasms are those of the ovary together with the endometrium. These constitute 40% of all, and carry a favourable prognosis because of low malignant potential. Cervical and ovarian malignancies are still rare, and if they occur they have similar histopathology due to direct spread of cervical malignancy to ovary.
Biomedical Journal of Scientific and Technical Research | 2017
Pallavi Mishra; Neha K Madan; Somshankar Chowdhury; Charanjeet Ahluwalia; Indrani Dhawan
Ewing Sarcoma Family of Tumours (ESFT) is uncommon, aggressive, malignant tumours that usually arise in soft tissue or bones in children and young adults. The term ESFT includes typical Ewing’s Sarcoma, the Peripheral Neuro ectodermal tumour (PNET) or Askin’stumor of the chest wall [1]. It is the second most malignant tumour in the 10-20 year age group [2]. ESFTs arise from migrating embryonic cells of the neural crest showing variable neuro ectodermal differentiation. The differentiation pattern forms the basis of differentiating each individual type of ESFT though these features commonly overlap. This tumour family most commonly involves long bones of lower limbs, however, atypical presentations have been studied, which can present a diagnostic challenge [3,4]. Here we present an exceptional case of Ewing’s Sarcoma presenting as a breast mass in a male patient.
Romanian journal of morphology and embryology | 2014
Poonam Jawanjal; Sudha Salhan; Indrani Dhawan; Richa Tripathi; Gayatri Rath
Journal of Mid-life Health | 2018
Gireesha Rawal; Sufian Zaheer; Amit Kumar Yadav; Indrani Dhawan
Journal of Mid-life Health | 2018
Sufian Zaheer; Gireesha Rawal; Indrani Dhawan
Annals of Applied Bio-Sciences | 2018
Neelam Sahani; Chintamani Pathak; Somshankar Chowdhury; Preeti Sharma; Shweta Sushmita; Indrani Dhawan
International journal of reproduction, contraception, obstetrics and gynecology | 2017
Gireesha Rawal; Charanjeet Ahluwalia; Amit Kumar Yadav; Indrani Dhawan