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V. V. S. S. Sagar

Publications (4)

Recent Modalities in the Diagnosis of Obesity

V. V. S. S. Sagar, A. K. Wanjari, Sourya Acharya & Sunil Kumar · Journal of Pharmaceutical Research International · 2021

Obesity has been an emerging health problem worldwide which has a major impact on public health. It is associated with medical, psychosocial and economic implications with increasing prevalence among both adult and paediatric population. Obesity led to an increased risk of medica...

Open access Research Article 10.9734/jpri/2021/v33i55A33817

Heart Failure Due to Secondary Haemochromatosis in a Case of Beta Thalassemia Major: A Rare Case Presentation

V. V. S. S. Sagar, Maharshi Patel, Pallavi Yelne, Shilpa Gaidhane & Chitturi Venkata Sai Akhil · Journal of Pharmaceutical Research International · 2021

Hemochromatosis is defined as abnormal accumulation of iron in various organs of the body such as liver, pancreas, skin, joints, heart due to raised gut absorption of iron due to low hepcidin yield. Hemochromatosis is secondary to thalassemia major in this case. In the absence of...

Open access Research Article 10.9734/jpri/2021/v33i48B33266

Efficacy of Intra-Lesional Bleomycin Sclerotherapy for the Treatment of Hemangioma-Case Report

Chitturi Venkata Sai Akhil, Sarika Bhimrao Gaikwad & V. V. S. S. Sagar · Journal of Pharmaceutical Research International · 2021

Vascular anomalies are one of the challenging diseases to manage, presenting in different age groups and with varied clinical course, of which hemangiomas are common which are vasoproliferative neoplasms and can occur in any organ. Depending on the age at presentation they are cl...

Open access Research Article 10.9734/jpri/2021/v33i51B33545

Hyperacute Gullain Barre Syndrome (GBS); The Catastrophic Variant- A Rare Case Report

Sourya Acharya, Amol andhale, Samarth Shukla, V. V. S. S. Sagar & Sunil Kumar · Journal of Pharmaceutical Research International · 2021

Guillain-Barré syndrome (GBS) also known as acute demyelinating polyradiculoneuropathy (AIDP) is an immunologically mediated  rare neurological disorder.  The  basic pathogenic mechanism is regulated by molecular mimicry. Usually there is a history of preceding infection which oc...

Open access Research Article 10.9734/jpri/2021/v33i53A33637