4.8 Article

Clinical, Immunological, and Molecular Profile of Chronic Granulomatous Disease: A Multi-Centric Study of 236 Patients From India

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Letter Allergy

Chronic Granulomatous Disease: A Perspective from a Developing Nation

Sathish Kumar Loganathan et al.

INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY (2021)

Article Immunology

Primary Immunodeficiencies in India: Molecular Diagnosis and the Role of Next-Generation Sequencing

Arun Kumar Arunachalam et al.

Summary: This study characterized the clinical and genetic spectrum of PID patients in India, identifying BTK and IL12RB1 as the most common mutated genes, with autosomal recessive and X-linked recessive inheritance in 51.6% and 23.7% of patients, respectively. MSMD and IL12RB1 mutations were more common in this population compared to the Western world and the Middle East.

JOURNAL OF CLINICAL IMMUNOLOGY (2021)

Letter Immunology

Infection Due to Serratia sp. in Chronic Granulomatous Disease-Is the Incidence Low in Tropical Countries?

Dharmagat Bhattarai et al.

JOURNAL OF CLINICAL IMMUNOLOGY (2021)

Article Immunology

Liver Abscess in Chronic Granulomatous Disease-Two Decades of Experience from a Tertiary Care Centre in North-West India

Rakesh Kumar Pilania et al.

Summary: This study presents the clinical features, microbiological profile, and treatment challenges faced in managing liver abscesses in CGD patients at a tertiary care center in North-West India, highlighting the necessity for prolonged antimicrobial treatment and the potential benefits of glucocorticoids in reducing inflammation for early resolution of abscesses in CGD. Data from developing countries are limited in literature on this topic.

JOURNAL OF CLINICAL IMMUNOLOGY (2021)

Article Allergy

Hemophagocytic Lymphohistiocytosis in Children with Chronic Granulomatous Disease-Single-Center Experience from North India

Pandiarajan Vignesh et al.

Summary: This study analyzed clinical and laboratory features of HLH in CGD patients in a tertiary-care center in North India. Among 80 patients diagnosed with CGD, 6.25% developed HLH, with infectious triggers including bloodstream infections, pneumonia, and splenic abscess. Notably, a child with X-linked CGD was infected with a fish pathogen, F. noatuensis. Early recognition and optimal management of both infectious trigger and HLH are important in preventing mortality.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE (2021)

Letter Immunology

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

Pandiarajan Vignesh et al.

JOURNAL OF CLINICAL IMMUNOLOGY (2019)

Review Immunology

Application of Flow Cytometry in Primary Immunodeficiencies: Experience From India

Manisha Rajan Madkaikar et al.

FRONTIERS IN IMMUNOLOGY (2019)

Article Medicine, Research & Experimental

Inherited p40phox deficiency differs from classic chronic granulomatous disease

Annemarie van de Geer et al.

JOURNAL OF CLINICAL INVESTIGATION (2018)

Article Multidisciplinary Sciences

A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease

Gudny A. Arnadottir et al.

NATURE COMMUNICATIONS (2018)

Review Medicine, General & Internal

Chronic granulomatous disease

Dirk Roos

BRITISH MEDICAL BULLETIN (2016)

Article Allergy

Chronic granulomatous disease: Review of a cohort of Egyptian patients

S. Meshaal et al.

ALLERGOLOGIA ET IMMUNOPATHOLOGIA (2015)

Article Immunology

Common Severe Infections in Chronic Granulomatous Disease

Beatriz E. Marciano et al.

CLINICAL INFECTIOUS DISEASES (2015)

Article Allergy

Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients

Mustafa Yavuz Koker et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2013)

Editorial Material Immunology

Corticosteroid Therapy for Liver Abscess in Chronic Granulomatous Disease

Jennifer W. Leiding et al.

CLINICAL INFECTIOUS DISEASES (2012)

Article Multidisciplinary Sciences

Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase

Chaim O. Jacob et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)

Article Immunology

Inheritance Pattern and Clinical Aspects of 93 Iranian Patients with Chronic Granulomatous Disease

Fatemeh Fattahi et al.

JOURNAL OF CLINICAL IMMUNOLOGY (2011)

Article Hematology

Hematologically important mutations: X-linked chronic granulomatous disease (third update)

Dirk Roos et al.

BLOOD CELLS MOLECULES AND DISEASES (2010)

Article Multidisciplinary Sciences

Chronic Granulomatous Disease: The European Experience

J. Merlijn van den Berg et al.

PLOS ONE (2009)

Article Pediatrics

Gastrointestinal involvement in chronic granulomatous disease

BE Marciano et al.

PEDIATRICS (2004)

Article Medicine, General & Internal

Chronic granulomatous disease - Report on a national registry of 368 patients

JA Winkelstein et al.

MEDICINE (2000)