Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Rajni Kumrah"'
Autor:
Rakesh Kumar Pilania, Suprit Basu, Jyoti Dixit, Rajni Kumrah, Ankur Kumar Jindal, Abarna Thangaraj, Ruby Nimesh, Taranpreet Kaur, Pandiarajan Vignesh, Deepti Suri, Amit Rawat, Sanjeev H. Naganur, Manphool Singhal, Shankar Prinja, Surjit Singh
Publikováno v:
The Lancet Regional Health - Southeast Asia, Vol 29, Iss , Pp 100474- (2024)
Summary: Background: Only limited information exists regarding the epidemiology of Kawasaki disease (KD) in low-income and middle-income countries. The present study provides the incidence of KD during 2015–2019 in Chandigarh, north India. Our cent
Externí odkaz:
https://doaj.org/article/30b2ec5139f04d70a7f8591bac654487
Autor:
K Gokul Das, Dharmagat Bhattarai, Anupriya Kaur, Anit Kaur, Rajni Kumrah, Priyanka Srivastava, Amit Rawat, Surjit Singh
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 11, Iss 9, Pp 5404-5409 (2022)
Background: Kawasaki disease is a pediatric, systemic, vasculitic disorder. Its exact etiology is still unknown. Genetic polymorphisms are being investigated as susceptibility factor for this disorder. These are likely to vary among different populat
Externí odkaz:
https://doaj.org/article/3026739c0b744d89a8e05de14cc68d87
Autor:
Rajni Kumrah, Rakesh Kumar Pilania, Nitin Kumar Menia, Amit Rawat, Jyoti Sharma, Anju Gupta, Pandiarajan Vignesh, Ankur Kumar Jindal, Rashmi Rikhi, Aniruddha Agarwal, Vishali Gupta, Surjit Singh, Deepti Suri
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
ObjectivesBlau syndrome (BS) is a rare autoinflammatory disease characterized by arthritis, dermatitis, and granulomatous uveitis in early childhood. The study presents the clinical experience of patients with BS at a tertiary care centre in Chandiga
Externí odkaz:
https://doaj.org/article/c329685c809845a79febb0d28b2b0427
Autor:
Pallavi L. Nadig, Vibhu Joshi, Rakesh Kumar Pilania, Rajni Kumrah, Jayakanthan Kabeerdoss, Saniya Sharma, Deepti Suri, Amit Rawat, Surjit Singh
Publikováno v:
Diagnostics, Vol 13, Iss 14, p 2338 (2023)
Kawasaki disease (KD) is an acute vasculitis of childhood that affects the medium vessels with a special predilection to the involvement of coronary arteries. The major morbidity of this disease is due to coronary artery aneurysm, which occurs in abo
Externí odkaz:
https://doaj.org/article/ecbd375b4fb142219292d286dc015af9
Autor:
Pandiarajan Vignesh, Gummadi Anjani, Rajni Kumrah, Ankita Singh, Sanjib Mondal, Johnson Nameirakpam, Ankur Jindal, Deepti Suri, Madhubala Sharma, Gurjit Kaur, Sathish Sharma, Kirti Gupta, Sreejesh Sreedharanunni, Amit Rawat, Surjit Singh
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
BackgroundHemophagocytic lymphohistiocytosis (HLH) is characterized by uncontrolled and excessive inflammation leading to high mortality. Aetiology of HLH can be primarily due to genetic causes or secondarily due to infections or rheumatological illn
Externí odkaz:
https://doaj.org/article/394ded5ac64e4d969a75dcbb91a71fae
Autor:
Priyanka Srivastava, Chitra Bamba, Rakesh Kumar Pilania, Anu Kumari, Rajni Kumrah, Archan Sil, Surjit Singh
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Kawasaki disease (KD) is a common childhood systemic vasculitis with a special predilection for coronary arteries. Even after more than five decades of the initial description of the disease, the etiology of KD remains an enigma. This transcriptome d
Externí odkaz:
https://doaj.org/article/121ffadb43ff42eaa6bbedfa55f8b222
Autor:
Rakesh Kumar Pilania, Aaqib Zaffar Banday, Saniya Sharma, Rajni Kumrah, Vibhu Joshi, Sathish Loganathan, Manpreet Dhaliwal, Ankur Kumar Jindal, Pandiarajan Vignesh, Deepti Suri, Amit Rawat, Surjit Singh
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Deficiency of adenosine deaminase type 2 (DADA2) was first described in 2014 as a monogenic cause of polyartertitis nodosa (PAN), early onset lacunar stroke and livedo reticularis. The clinical phenotype of DADA2 is, however, very broad and may invol
Externí odkaz:
https://doaj.org/article/223e1c101b4d42568a0af83dfeec659c
Autor:
Rajni Kumrah, Pandiarajan Vignesh, Pratap Patra, Ankita Singh, Gummadi Anjani, Poonam Saini, Madhubala Sharma, Anit Kaur, Amit Rawat
Publikováno v:
Genes and Diseases, Vol 7, Iss 1, Pp 52-61 (2020)
Severe Combined Immunodeficiency (SCID) is an inherited group of rare, life-threatening disorders due to the defect in T cell development and function. Clinical manifestations are characterised by recurrent and severe bacterial, viral, and fungal opp
Externí odkaz:
https://doaj.org/article/937e62e189b24fb29e8720ad81cee598
Autor:
Aaqib Zaffar Banday, Sanjib Mondal, Prabal Barman, Archan Sil, Rajni Kumrah, Pandiarajan Vignesh, Surjit Singh
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Rheumatic heart disease (RHD), the principal long-term sequel of acute rheumatic fever (ARF), has been a major contributor to cardiac-related mortality in general population, especially in developing countries. With improvement in health and sanitati
Externí odkaz:
https://doaj.org/article/66a5ee8a1c1a4092a1309078ebdb1e51
Publikováno v:
European Journal of Rheumatology, Vol 9, Iss 1, Pp 58-59 (2022)
Externí odkaz:
https://doaj.org/article/4adf018534b44d80943f48f6b205c966