Kaur A - Search Results

1

Successful perioperative management of three patients with hereditary angioedema without C1 esterase inhibitor therapy: A developing country perspective.

Jindal AK, Singh A, Anjani G, Kaur A, Jaiswal M, Chopra S, Saini U, Mahajan S, Rawat A, Singh S, Longhurst H. Jindal AK, et al. Among authors: kaur a. Immunobiology. 2020 Nov;225(6):152022. doi: 10.1016/j.imbio.2020.152022. Epub 2020 Nov 3. Immunobiology. 2020. PMID: 33197705

2

When Transient Lymphopenia Mimics SCID!

Rawat A, Vignesh P, Kaur A. Rawat A, et al. Among authors: kaur a. Indian J Pediatr. 2019 Jul;86(7):574-575. doi: 10.1007/s12098-019-02988-3. Epub 2019 Jun 6. Indian J Pediatr. 2019. PMID: 31172390 Review. No abstract available.

3

Myriad Faces of Chronic Granulomatous Disease: All in an Indian Family with Novel CYBB Defect.

Vignesh P, Sharma M, Pilania RK, Shandilya JK, Kaur A, Goel S, Kaur A, Suri D, Rawat A, Dalal A, Sarma AS, Singh S. Vignesh P, et al. Among authors: kaur a. J Clin Immunol. 2019 Aug;39(6):611-615. doi: 10.1007/s10875-019-00661-0. Epub 2019 Jul 23. J Clin Immunol. 2019. PMID: 31338742 No abstract available.

4

A young girl with hypogammaglobulinemia and granulomatous hepatitis caused by a novel mutation in ZBTB24 gene: A case based analysis.

Banday AZ, Jindal AK, Kaur A, Kumar Y, Nameirakpam J, Patra PK, Rawat A. Banday AZ, et al. Among authors: kaur a. Immunobiology. 2020 May;225(3):151912. doi: 10.1016/j.imbio.2020.151912. Epub 2020 Feb 10. Immunobiology. 2020. PMID: 32061411

5

Genetics of severe combined immunodeficiency.

Kumrah R, Vignesh P, Patra P, Singh A, Anjani G, Saini P, Sharma M, Kaur A, Rawat A. Kumrah R, et al. Among authors: kaur a. Genes Dis. 2019 Jul 24;7(1):52-61. doi: 10.1016/j.gendis.2019.07.004. eCollection 2020 Mar. Genes Dis. 2019. PMID: 32181275 Free PMC article. Review.

6

An update on the genetics and pathogenesis of hereditary angioedema.

Banday AZ, Kaur A, Jindal AK, Rawat A, Singh S. Banday AZ, et al. Among authors: kaur a. Genes Dis. 2019 Aug 1;7(1):75-83. doi: 10.1016/j.gendis.2019.07.002. eCollection 2020 Mar. Genes Dis. 2019. PMID: 32181278 Free PMC article. Review.

7

Splice-site mutation in COPA gene and familial arthritis - a new frontier.

Banday AZ, Kaur A, Jindal AK, Patra PK, Guleria S, Rawat A. Banday AZ, et al. Among authors: kaur a. Rheumatology (Oxford). 2021 Jan 5;60(1):e7-e9. doi: 10.1093/rheumatology/keaa354. Rheumatology (Oxford). 2021. PMID: 32778887 No abstract available.

8

Epstein-Barr virus-associated lymphocytic cholangitis in a child with X-linked lymphoproliferative syndrome.

Bhattarai D, Vignesh P, Kaur A, Kumari P, V Menon J, Geethanjali G, Rawat A. Bhattarai D, et al. Among authors: kaur a. Scand J Immunol. 2021 Feb;93(2):e12975. doi: 10.1111/sji.12975. Epub 2020 Sep 23. Scand J Immunol. 2021. PMID: 32897580 Free article. No abstract available.

9

Deforming Polyarthritis in a North Indian Family-Clinical Expansion of STING-Associated Vasculopathy with Onset in Infancy (SAVI).

Anjani G, Jindal AK, Prithvi A, Kaur A, Rawat A, Sharma M, Yuan B, Chinn IK, Singh S. Anjani G, et al. Among authors: kaur a. J Clin Immunol. 2021 Jan;41(1):209-211. doi: 10.1007/s10875-020-00872-w. Epub 2020 Sep 24. J Clin Immunol. 2021. PMID: 32974768 No abstract available.

10

Cutaneous IgA vasculitis-presenting manifestation of a novel mutation in the IKZF1 gene.

Banday AZ, Jindal AK, Kaur A, Saka R, Parwaiz A, Sachdeva MUS, Rawat A. Banday AZ, et al. Among authors: kaur a. Rheumatology (Oxford). 2021 Mar 2;60(3):e101-e103. doi: 10.1093/rheumatology/keaa492. Rheumatology (Oxford). 2021. PMID: 33097959 No abstract available.

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