Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Suhas K, Ganguli"'
Publikováno v:
European Medical Journal Rheumatology, Vol 4, Iss 1, Pp 90-97 (2017)
Systemic lupus erythematosus (SLE) is a chronic, multi-organ disease that predominantly affects young women of childbearing age. It is also a disease in which epigenetic modulation is emerging as an important mechanism for understanding how the envir
Externí odkaz:
https://doaj.org/article/0a07327ad075419db839f7656d8b691c
Publikováno v:
Lupus. 29:1781-1789
Objective To evaluate the reliability, validity, feasibility and psychometric performance of the Lupus Impact Tracker (LIT) as a patient reported outcome (PRO) measure tool in pediatric systemic lupus erythematosus (pSLE). Methods This is a prospecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cf260d80492befcaf9c5ab365d27124
https://doi.org/10.1177/0961203320951264
https://doi.org/10.1177/0961203320951264
Publikováno v:
Journal of Pediatric Infectious Diseases. :091-094
Hemophagocytic lymphohistiocytosis comes under the category of histiocytosis type II. It can be of two types, namely familial hemophagocytic lymphohistiocytosis and infection associated hemophagocytic syndrome. The latter is commonly associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::141ee4a8fdd9961cdb008ba23e155dbe
https://doi.org/10.3233/jpi-2010-0213
https://doi.org/10.3233/jpi-2010-0213
Publikováno v:
Journal of Pediatric Infectious Diseases. :209-211
Kala-azar is a common condition prevalent in several parts of India. The typical clinical presentation includes fever, gross emaciation, anemia, hepatosplenomegaly. Several other clinical patterns of involvement have been identified. We report a case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa3426ade5f338881546bfcee65949dd
https://doi.org/10.1055/s-0035-1556989
https://doi.org/10.1055/s-0035-1556989
Publikováno v:
Indian pediatrics. 46(7)
We report clinico-serological profile of 210 children with Juvenile idiopathic arthritis (JIA), diagnosed as per ILAR classification criteria. Polyarticular, oligoarticular, and systemic onset disease was observed in 72, 69, and 40 children, respecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::03a37e94fbe06ecce1a655031c914c38
https://pubmed.ncbi.nlm.nih.gov/19638666
https://pubmed.ncbi.nlm.nih.gov/19638666