Brothers with constrictive pericarditis – A novel mutation in a rare disease-Reference-Cited by-同舟云学术

Brothers with constrictive pericarditis – A novel mutation in a rare disease

Published:2016-09 Issue: Volume:68 Page:S284-S287
ISSN:0019-4832
Container-title:Indian Heart Journal
language:en
Short-container-title:Indian Heart Journal

Author:

Patil Devendra V.,Phadke Milind S.,Pahwa Jivtesh S.,Dalal Ashwin B.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference3 articles.

1. Novel mutations in PRG4 gene in two Indian families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome;Nandagopalan;Indian J Med Res,2014

2. Synovial pathology in camptodactyly-arthropathy-coxa vara-pericarditis syndrome;Shayan;Pediatr Dev Pathol,2005

3. Camptodactyly-arthropathy-coxa vara-pericarditis Syndrome versus juvenile idiopathic arthropathy;Offiah;AJR Am J Roentgenol,2005

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1. Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome;BMJ Case Reports;2024-07

2. Thirteen Indians with camptodactyly-arthropathy-coxa vara-pericarditis syndrome;Clinical Dysmorphology;2024-03-22

3. A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report;Pediatric Rheumatology;2023-01-24

4. Pseudo-rheumatic manifestations of limping: Camptodactyly–arthropathy–coxa vara–pericarditis syndrome: Single case report and review of the literature;Frontiers in Pediatrics;2022-12-05

5. Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Resembling Juvenile Idiopathic Arthritis: A Single-Center Experience from Southern Turkey;Molecular Syndromology;2021