Detalhe da pesquisa
1.
Inborn Errors of Immunity-the Sri Lankan Experience 2010-2022.
J Clin Immunol
; 43(8): 1858-1872, 2023 11.
Artigo
Inglês
| MEDLINE | ID: mdl-37480474
2.
A rare mutation causing autosomal dominant STAT1 deficiency in a South African multiplex kindred with disseminated BCG infection.
BMC Pediatr
; 23(1): 378, 2023 07 29.
Artigo
Inglês
| MEDLINE | ID: mdl-37516851
3.
Excessive deubiquitination of NLRP3-R779C variant contributes to very-early-onset inflammatory bowel disease development.
J Allergy Clin Immunol
; 147(1): 267-279, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32941940
4.
Liver Abscess in Chronic Granulomatous Disease-Two Decades of Experience from a Tertiary Care Centre in North-West India.
J Clin Immunol
; 41(3): 552-564, 2021 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33387158
5.
Accelerated Immunodeficiency-associated Vaccine-derived Poliovirus Serotype 3 Sequence Evolution Rate in an 11-week-old Boy With X-linked Agammaglobulinemia and Perinatal Human Immunodeficiency Virus Exposure.
Clin Infect Dis
; 70(1): 132-135, 2020 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31086993
6.
Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families.
J Clin Immunol
; 40(1): 96-104, 2020 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31696364
7.
RASGRP1 mutation in autoimmune lymphoproliferative syndrome-like disease.
J Allergy Clin Immunol
; 142(2): 595-604.e16, 2018 08.
Artigo
Inglês
| MEDLINE | ID: mdl-29155103
8.
Clinical and molecular features of X-linked hyper IgM syndrome - An experience from North India.
Clin Immunol
; 195: 59-66, 2018 10.
Artigo
Inglês
| MEDLINE | ID: mdl-30053428
9.
X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations.
J Clin Immunol
; 36(3): 187-94, 2016 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-26931785
10.
X-linked agammaglobulinemia: Twenty years of single-center experience from North West India.
Ann Allergy Asthma Immunol
; 117(4): 405-411, 2016 10.
Artigo
Inglês
| MEDLINE | ID: mdl-27593100
11.
Prevalence of BTK mutations in male Algerian patterns with agammaglobulinemia and severe B cell lymphopenia.
Clin Immunol
; 161(2): 286-90, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26387629
12.
NF-E2 mutation as a novel cause for inherited thrombocytopenia.
Br J Haematol
; 189(2): e41-e44, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-31951293
13.
Chronic granulomatous disease: two decades of experience from a tertiary care centre in North West India.
J Clin Immunol
; 34(1): 58-67, 2014 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-24276928
14.
Homozygous transcription factor 3 gene (TCF3) mutation is associated with severe hypogammaglobulinemia and B-cell acute lymphoblastic leukemia.
J Allergy Clin Immunol
; 140(4): 1191-1194.e4, 2017 10.
Artigo
Inglês
| MEDLINE | ID: mdl-28532655
15.
The genetic and clinical characteristics and effects of Canakinumab on cryopyrin-associated periodic syndrome: a large pediatric cohort study from China.
Front Immunol
; 14: 1267933, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37809096
16.
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease.
J Exp Med
; 220(5)2023 05 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36884218
17.
Penicilliosis in children without HIV infection--are they immunodeficient?
Clin Infect Dis
; 54(2): e8-e19, 2012 Jan 15.
Artigo
Inglês
| MEDLINE | ID: mdl-22065867
18.
Fatal SARS in X-Linked Lymphoproliferative Disease Type 1: A Case Report.
Front Pediatr
; 10: 794110, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35498795
19.
Diagnostic challenge in a series of eleven patients with hyper IgE syndromes.
Front Immunol
; 13: 1057679, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-36703986
20.
Meningoencephalitis in primary antibody deficiency: Our experience from northwest India.
J Neuroimmunol
; 371: 577952, 2022 10 15.
Artigo
Inglês
| MEDLINE | ID: mdl-36030644