Rashmi Rikhi
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Explore the profile of Rashmi Rikhi including associated specialties, affiliations and a list of published articles.
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12
Citations
47
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Recent Articles
1.
Rikhi R, Basu S, Arora K, Chan K, Jindal A, Rawat A, et al.
Scand J Immunol
. 2024 Sep;
100(5):e13408.
PMID: 39304328
This report describes two brothers from India and a Chinese patient with somatic reversion of an inherited deleterious mutation in the WAS gene. Both the Indian siblings had inherited a...
2.
Basu S, Rikhi R, Arora K, Joshi V, Sharma S, Rawat A, et al.
Pediatr Blood Cancer
. 2024 Mar;
71(6):e30972.
PMID: 38523275
Introduction: Wiskott-Aldrich syndrome (WAS) is a rare X-linked inborn error of immunity characterized by microthrombocytopenia, infections, eczema, and increased predisposition to develop autoimmunity and malignancy. Flow cytometric assay for determining...
3.
Jindal A, Mondal S, Sil A, Rawat A, Chawla S, Tyagi R, et al.
Int Arch Allergy Immunol
. 2024 Jan;
185(4):370-381.
PMID: 38194943
Introduction: X-linked lymphoproliferative syndrome (XLP) is a rare primary immune deficiency. Two types of XLP have been described: XLP-1 and XLP-2. Methods: We found 7 patients with XLP (3 had...
4.
Patra P, Jindal A, Rikhi R, Kaur A, Srivastava P, Suri D, et al.
Front Pediatr
. 2023 Oct;
11:1252024.
PMID: 37808562
Introduction: gene single-nucleotide polymorphisms (SNPs) have been associated with susceptibility and development of coronary artery abnormalities (CAAs) in children with Kawasaki disease (KD) in Japanese, Chinese, and Taiwanese populations. However,...
5.
Kumrah R, Pilania R, Kumar Menia N, Rawat A, Sharma J, Gupta A, et al.
Front Immunol
. 2022 Oct;
13:932919.
PMID: 36189202
Objectives: Blau 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...
6.
Gupta P, Subburaj K, Jindal A, Rawat A, Rikhi R, De D, et al.
Clin Exp Dermatol
. 2022 Mar;
47(5):1013-1016.
PMID: 35249234
Primary immunodeficiencies with eczema can be easily misdiagnosed as atopic eczema, and thus require a high degree of awareness for diagnosis. Wiskott-Aldrich syndrome (WAS) is a rare disease and the...
7.
Jindal A, Rastogi P, Anjani G, Rikhi R, Rawat A, Ahluwalia J
Pediatr Dev Pathol
. 2022 Mar;
25(3):345-350.
PMID: 35236172
Wiskott-Aldrich Syndrome (WAS) is an inherited disorder characterized by the classical triad of eczema, micro-thrombocytopenia, and immune deficiency. This disease affects the hematopoietic cells to a variable extent. The spectrum...
8.
Sudhakar M, Rikhi R, Loganathan S, Suri D, Singh S
Appl Clin Genet
. 2021 Aug;
14:363-388.
PMID: 34447261
Wiskott-Aldrich syndrome (WAS) is an uncommon X-linked combined-immunodeficiency disorder characterized by a triad of thrombocytopenia, eczema, and immunodeficiency. Patients with WAS are also predisposed to autoimmunity and malignancy. Autoimmune manifestations...
9.
Suri D, Rikhi R, Jindal A, Rawat A, Sudhakar M, Vignesh P, et al.
Front Immunol
. 2021 May;
12:627651.
PMID: 33936041
Background: Wiskott Aldrich syndrome (WAS) is characterized by bleeding manifestations, recurrent infections, eczema, autoimmunity, and malignancy. Over the last decade, improved awareness and better in-house diagnostic facilities at several centers...
10.
Nameirakpam J, Rikhi R, Singh Rawat S, Sharma J, Suri D
Genes Dis
. 2020 Mar;
7(1):93-106.
PMID: 32181280
Inflammatory bowel disease (IBD) is more common in adults than in children. Onset of IBD before 17 years of age is referred as pediatric onset IBD and is further categorized...