Suchergebnisse - "Jindal, Ankur Kumar"

PubPharm (20)

1

Heterozygous RAD50 gene variant in a family with systemic sclerosis suggests role of impaired DNA repair mechanisms in disease pathogenesis

enthalten in: Clinical and experimental dermatology | 2024

von Machhua, S. | Sharma, S. | Minz, R. | +4

2

Recalcitrant skin ulcers in a patient with Papillon-Lefèvre syndrome : an unusual novel presentation

enthalten in: Clinical and experimental dermatology | 2024

von Malhi, K. | Singh, S. | Mustari, A. | +3

3

A collaborative study for incomplete Kawasaki disease in Asia

enthalten in: International journal of rheumatic diseases | 2023

von Yu, X. | Yang, M. | Jindal, A. | +5

4

A young boy with rash, arthritis, and developmental delay : Monogenic lupus due to DNASE2 gene defect

enthalten in: International journal of rheumatic diseases | 2023

von Basu, S. | Sil, A. | Jindal, A. | +4

5

Disseminated Mycobacterium fortuitum infection in a young girl with IFN-γR1 defect masquerading as histiocytosis

enthalten in: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology | 2023

von Sil, A. | Basu, S. | Das, J. | +5

6

Correspondence on 'Points to consider for the treatment of immune-mediated inflammatory diseases with Janus kinase inhibitors : a consensus statement'

enthalten in: Annals of the rheumatic diseases | 2023

von Banday, A. | Jindal, A. | Singh, S.

CommentOn: Ann Rheum Dis. 2021 Jan;80(1):71-87. - PMID 33158881

7

Negative pressure flash pulmonary edema in a child with hereditary angioedema

enthalten in: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology | 2022

von Barman, P. | Basu, S. | Thakur, I. | +5

8

Cutaneous involvement in DOCK8-related immunodeficiency syndrome responding to thalidomide

enthalten in: Dermatologic therapy | 2022

von Dev, A. | Sil, A. | Jindal, A. | +3

9

Transient neutropenia in Kawasaki disease : Is it the disease, drugs or both?

enthalten in: Pediatric blood & cancer | 2021

von Patra, P. | Banday, A. | Jindal, A. | +2

10

Deficiency of Adenosine Deaminase 2-a Monogenic Cause of Wunderlich Syndrome

enthalten in: Journal of clinical immunology | 2021

von Patra, P. | Mondal, S. | Singhal, M. | +4