Vignesh Pandiarajan
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Explore the profile of Vignesh Pandiarajan including associated specialties, affiliations and a list of published articles.
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31
Citations
101
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Recent Articles
1.
Sharma R, Basu S, Tyagi R, Siniah S, Barman P, Sil A, et al.
Asia Pac Allergy
. 2025 Mar;
15(1):1-6.
PMID: 40051425
Background: Hereditary angioedema (HAE) is characterized by unpredictable acute attacks that impair the patient's quality of life (QoL) not only due to the impact on functional abilities caused by edema...
2.
Jindal A, Basu S, Tyagi R, Barman P, Sil A, Chawla S, et al.
Clin Exp Dermatol
. 2023 Dec;
49(4):368-374.
PMID: 38039144
Background: Hereditary angio-oedema (HAE) is a rare autosomal dominant disorder characterized clinically by recurrent episodes of nonpruritic subcutaneous and/or submucosal oedema. Laryngeal oedema is the commonest cause of mortality in...
3.
Saini M, Khadwal A, Roy S, Pandiarajan V, Malhotra P
Cureus
. 2023 Oct;
15(9):e45159.
PMID: 37842439
Severe combined immunodeficiency (SCID) is an inborn error of immunity invariably resulting in mortality in infancy until managed by hematopoietic stem cell transplant (HSCT). We present an unusual case of...
4.
Jindal A, Sil A, Aggarwal R, Tyagi R, Mondal S, Singh A, et al.
Clin Exp Dermatol
. 2023 Oct;
49(3):226-234.
PMID: 37815217
Background: Dedicator of cytokinesis protein 8 (DOCK8) deficiency is an autosomal recessive form of combined immunodeficiency. This rare disorder is characterized by an increased predisposition to allergy, autoimmunity and malignancies....
5.
Banday A, Babbar A, Patra P, Jindal A, Suri D, Pandiarajan V, et al.
J Trop Pediatr
. 2023 Aug;
69(3).
PMID: 37608506
Various factors (e.g., infections) have been postulated to trigger Kawasaki disease (KD) in genetically predisposed individuals. Whether neoplasms can trigger KD is largely unknown due to paucity of data. Herein,...
6.
Sharma R, Chaudhary H, Patra P, Sudhakar M, Anjani G, Jindal A, et al.
J Family Med Prim Care
. 2023 Mar;
11(12):7920-7925.
PMID: 36994004
Aim: To assess distress, insomnia, and psychosocial impact of SARS-CoV-2 outbreak on children with SLE and their caregivers. Methods: Patients with pSLE undergoing treatment in the Department of Pediatrics, PGIMER,...
7.
Basu A, Saharan P, Katoch G, Dash N, Pandiarajan V, Mewara A
Trop Doct
. 2023 Jan;
53(2):317-318.
PMID: 36694454
Visceral leishmaniasis is the most severe form of leishmaniasis. There has been an increase in number of cases in the sub-Himalayan regions of India in the past few years. Here...
8.
Jindal A, Handa S, Loganathan S, Sudhakar M, Kaushik A, Suri D, et al.
J Eur Acad Dermatol Venereol
. 2022 Nov;
37(3):598-604.
PMID: 36413107
Background: Juvenile localized scleroderma (JLS) or morphoea, a rare chronic autoimmune disease predominantly affects skin, subcutaneous tissue and occasionally the adjacent muscle, fascia and bone. We report the largest single-centre...
9.
Jindal A, Suri D, Gupta K, Kumar A, Pandiarajan V, Pilania R, et al.
Clin Neuropathol
. 2022 Oct;
42(1):15-25.
PMID: 36278299
Purpose: To describe the neuropathological findings in two patients with primary immunodeficiency who had fatal viral encephalitis. Materials And Methods: Severe combined immunodeficiency (SCID) was confirmed in case 1 by...
10.
Jindal A, Chaudhary H, Tyagi R, Rawat A, Suri D, Patra P, et al.
J Neuroimmunol
. 2022 Aug;
371:577952.
PMID: 36030644
Background/objectives: Patients with primary antibody deficiency (PAD) are predisposed to develop meningoencephalitis, often considered to be enteroviral. However, there is a paucity of literature on this subject, and there are...