Clinical and Genetic Profile of X-Linked Agammaglobulinemia: A Multicenter Experience From India.

doi:10.3389/fimmu.2020.612323

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Clinical and Genetic Profile of X-Linked Agammaglobulinemia: A Multicenter Experience From India.

Frontiers in immunology - 1 Jan 2020

Rawat Amit, Jindal Ankur Kumar, Suri Deepti, Vignesh Pandiarajan, Gupta Anju, Saikia Biman, Minz Ranjana W, Banday Aaqib Zaffar, Tyagi Rahul, Arora Kanika, Joshi Vibhu, Mondal Sanjib, Shandilya Jitendra Kumar, Sharma Madhubala, Desai Mukesh, Taur Prasad, Pandrowala Ambreen, Gowri Vijaya, Sawant-Desai Sneha, Gupta Maya, Dalvi Aparna Dhondi, Madkaikar Manisha, Aggarwal Amita, Raj Revathi, Uppuluri Ramya, Bhattad Sagar, Jayaram Ananthvikas, Lashkari Harsha Prasad, Rajasekhar Liza, Munirathnam Deenadayalan, Kalra Manas, Shukla Anuj, Saka Ruchi, Sharma Rajni, Garg Ravinder, Imai Kohsuke, Nonoyama Shigeaki, Ohara Osamu, Lee Pamela P, Chan Koon Wing, Lau Yu-Lung, Singh Surjit

Abstract excerpt

Background: There is paucity of literature on XLA from developing countries. Herein we report the clinical and molecular profile and outcome in a multicenter cohort of patients with XLA from India. Methods: Data on XLA from all regional centers supported by the Foundation for Primary Immunodeficiency Diseases (FPID), USA and other institutions providing care to patients with PIDs were collated. Diagnosis of XLA...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Agammaglobulinaemia Tyrosine Kinase

Share to Agammaglobulinemia

Share to Arthritis

Share to Genetic Diseases, X-Linked

Share to Genetic Profile

Share to Immunoglobulins, Intravenous

Share to India

Share to Protein-Tyrosine Kinases

Source

Open in PubMed Open full text

Identifiers

PMID: 33584693
DOI: 10.3389/fimmu.2020.612323
PMCID: PMC7873890

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical and Genetic Profile of X-Linked Agammaglobulinemia: A Multicenter Experience From India.PMID 33584693Read ↗

Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India.Semantic proximity Read ↗

X-linked agammaglobulinemia: Twenty years of single-center experience from North West India.Semantic proximity Read ↗

Clinical features and mutational analysis of X-linked agammaglobulinemia patients in MalaysiaSemantic proximity Read ↗

A Registry Study of 240 Patients with X-Linked Agammaglobulinemia Living in the USA.Semantic proximity Read ↗

Clinical characteristics and genetic profiles of 174 patients with X-linked agammaglobulinemia: Report from Shanghai, China (2000-2015).Semantic proximity Read ↗

Distinct Clinical Features and Novel Mutations in Taiwanese Patients With X-Linked Agammaglobulinemia.Semantic proximity Read ↗

Clinical characteristics and genotype-phenotype correlation in 62 patients with X-linked agammaglobulinemia.Semantic proximity Read ↗

Outcomes of X-Linked Agammaglobulinaemia Patients.Semantic proximity Read ↗

Agammaglobulinemia: from X-linked to Autosomal Forms of Disease.Semantic proximity Read ↗

Retrospective study of 98 patients with X-linked agammaglobulinemia complicated with arthritis.Semantic proximity Read ↗

Clinical and genetic profiles of patients with X-linked agammaglobulinemia from southeast Turkey: Novel mutations in BTK gene.Semantic proximity Read ↗

[Clinical features of X-linked agammaglobulinemia: analysis of 8 cases].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.