Priya Treesa Thomas
Overview
Explore the profile of Priya Treesa Thomas including associated specialties, affiliations and a list of published articles.
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Articles
40
Citations
150
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Recent Articles
1.
Singh B, Lipunga G, Thangavelu P, Dhar S, Ferreira Cronemberger L, Abhilash K, et al.
Lancet
. 2025 Mar;
PMID: 40081400
Background: Brain infections pose substantial challenges in diagnosis and management and carry high mortality and morbidity, especially in low-income and middle-income countries. We aimed to improve the diagnosis and early...
2.
Baskar D, Vengalil S, Polavarapu K, Preethish-Kumar V, Nashi S, Arunachal G, et al.
J Neuromuscul Dis
. 2025 Mar;
:22143602241313119.
PMID: 40033712
Introduction: Titinopathies are heterogenous group of disorders affecting the skeletal and cardiac muscles variably and caused by Titin ( gene mutations located in Chromosome 2. The manifestations extend from congenital...
3.
Arshad F, Hurzuk S, Tiwari M, Varghese F, Hoskeri R, Paplikar A, et al.
Curr Alzheimer Res
. 2024 Nov;
21(7):470-478.
PMID: 39601170
Introduction: The COVID-19 pandemic has had multifaceted and enduring impacts on people with dementia and their caregivers; however, our understanding of the long-term outcomes remains limited. We aimed to explore...
4.
D Keerthana , Arun M, Kumar G, Desai G, Thomas P, Netravathi M
Indian J Psychol Med
. 2024 Nov;
:02537176241264772.
PMID: 39564228
No abstract available.
5.
Zacharias L, Thomas P, Warrier M, Yadav R, Alladi S, Nalini A, et al.
Indian J Palliat Care
. 2024 Oct;
30(3):232-238.
PMID: 39371494
Objectives: Neurodegenerative disorders necessitate comprehensive palliative care due to their progressive and irreversible nature. Limited studies have explored the comprehensive assessment needs of this population. This present study is designed...
6.
Santhappan Girija M, Menon D, Polavarapu K, Preethish-Kumar V, Vengalil S, Nashi S, et al.
Ann Indian Acad Neurol
. 2024 Sep;
27(5):552-557.
PMID: 39344256
Background And Objectives: Cardiovascular magnetic resonance imaging (CMRI) is the noninvasive technique of choice for early detection of cardiac involvement in Duchenne and Becker muscular dystrophy (DMD and BMD, respectively),...
7.
Baby P, Thomas P, P B, J J, Kumar G, M A, et al.
J Neurosci Nurs
. 2024 Sep;
56(6):239-244.
PMID: 39331627
BACKGROUND: Wilson disease (WD) is a rare disease characterized by impaired copper metabolism. It is usually diagnosed in children and has several distinct attributes that can make the caregiving experience...
8.
Baskar D, Reddy N, Preethish-Kumar V, Polavarapu K, Nishadham V, Vengalil S, et al.
J Neuromuscul Dis
. 2024 Aug;
11(5):959-968.
PMID: 39213088
Introduction: GNE myopathy is a rare slowly progressive adult-onset distal myopathy with autosomal recessive inheritance. It has distinctive features of quadriceps sparing with preferential anterior tibial involvement. Most patients eventually...
9.
Kumar D, Thomas P, Kumar G, M A, Sahoo S, Sadasivan A, et al.
Disabil Rehabil
. 2024 Aug;
:1-8.
PMID: 39180333
Purpose: Duchenne muscular dystrophy (DMD), a genetically linked muscle disease, is one of the most devastating diseases with currently no cure. Developing essential social skills as a child moves into...
10.
Suma R, Netravathi M, Gururaj G, Thomas P, Singh B, Solomon T, et al.
J Glob Infect Dis
. 2024 Jan;
15(4):156-165.
PMID: 38292694
Introduction: Encephalitis is a major public health problem worldwide that causes huge emotional and economic loss to humanity. Encephalitis, being a serious illness, affects people of all ages. The aim...