Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Chetna Khemani"'
Autor:
Sumant Prabhudesai, Chetna Khemani
Publikováno v:
Journal of Pediatric Critical Care, Vol 6, Iss 6, Pp 47-50 (2019)
Hypertensive emergencies commonly occur due to an underlying renal or reno-vascular disease. Vasculitis is an uncommon cause. We report a 5 year old boy who presented with hypertension, heart failure and posterior reversible encephalopathy syndrome (
Externí odkaz:
https://doaj.org/article/0e383ff2c41b4142b4bd4712438d1f5c
Autor:
Archana Khan, Hiren Panwala, Aditya Daftary, Raju Khubchandani, Chetna Khemani, Pallavi Pimpale Chavan, Ivona Aksentijevich
Publikováno v:
The Journal of Rheumatology. 48:1850-1855
ObjectiveMajeed syndrome (MJS) is an autosomal recessive, systemic autoinflammatory disease (SAID) caused by biallelic loss-of-function variants in theLPIN2gene. It is characterized by early-onset chronic recurrent multifocal osteomyelitis (CRMO), dy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10e4bd1fb539c780bc11dabab19db9dd
https://doi.org/10.3899/jrheum.201663
https://doi.org/10.3899/jrheum.201663
Autor:
Chetna Khemani, Sumant Prabhudesai
Publikováno v:
Journal of Pediatric Critical Care, Vol 6, Iss 6, Pp 47-50 (2019)
Hypertensive emergencies commonly occur due to an underlying renal or reno-vascular disease. Vasculitis is an uncommon cause. We report a 5 year old boy who presented with hypertension, heart failure and posterior reversible encephalopathy syndrome (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65f1160a36650e2f404935b822aceafd
https://doi.org/10.21304/2019.0606.00548
https://doi.org/10.21304/2019.0606.00548
Autor:
Chetna Khemani, Raju Khubchandani
Publikováno v:
Pediatric Rheumatology ISBN: 9789811017490
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6af10084370b39448ccf9b982a464f60
https://doi.org/10.1007/978-981-10-1750-6_15
https://doi.org/10.1007/978-981-10-1750-6_15
Autor:
Carlos D. Rose, Rachana Hasija, Raju Khubchandani, Isabelle Touitou, Chetna Khemani, Carine Wouters
Publikováno v:
The Journal of Rheumatology. 39:1888-1892
Objective.To put forward a new concept — Blau arteritis, a form of large-vessel vasculitis phenotypically related to Takayasu disease but genetically and clinically part of an expanded phenotype of Blau syndrome.Methods.We provide a clinical descri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe8dfca324ea24f4bbb5b0fd5e0ab59f
https://doi.org/10.3899/jrheum.120156
https://doi.org/10.3899/jrheum.120156
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 9, Iss Suppl 1, p P37 (2011)
Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal
Methods Retrospective chart review of the demographic, clinical, diagnostic and genetic characteristics were studied. Results Over seven years, 12 of 1214 new cases seen in the Pediatric Rheumatology Clinic (1%) (M: F = 1:1), were diagnosed as Sarcoi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5531b6318183b5394890eb6458bfa928
https://doaj.org/article/5edd2d96cc9242f78cf34f56a21718e5
https://doaj.org/article/5edd2d96cc9242f78cf34f56a21718e5
Autor:
Chetna, Khemani, Raju, Khubchandani
Publikováno v:
Indian pediatrics. 44(12)
CINCA syndrome is a genetic disorder characterized by early onset of recurrent fever, rash, progressive articular and neurological involvement. We report a 7-year-old girl with CINCA syndrome with an infrequent manifestation of retinal vasculitis and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f3e0531a9c3d5828db9f2426d551b90d
https://pubmed.ncbi.nlm.nih.gov/18175851
https://pubmed.ncbi.nlm.nih.gov/18175851
Autor:
Chetna, Khemani, Raju, Khubchandani
Publikováno v:
Indian pediatrics. 44(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::39fb370a2d523aabee13449f74accbe4
https://pubmed.ncbi.nlm.nih.gov/17277434
https://pubmed.ncbi.nlm.nih.gov/17277434
Autor:
Raju Khubchandani, Chetna Khemani
Publikováno v:
The Indian Journal of Pediatrics. 73:545-546
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d87a3a1bbc2692a531d881aaade0173
https://doi.org/10.1007/bf02759910
https://doi.org/10.1007/bf02759910
Publikováno v:
Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal, Vol 9, Iss Suppl 1, p P36 (2011)
Pediatric Rheumatology Online Journal, Vol 9, Iss Suppl 1, p P36 (2011)
Description MG, now a 10 year old female, was seen with a history of recurrent fevers since 1 month of life with bilateral knee effusions noted at 1.5 years of age, in the year 2002. This was initially treated as ANA negative oligoarticular JIA, requ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a38fd2260b5db4dbd5b8adb506a994f
http://europepmc.org/articles/PMC3194693
http://europepmc.org/articles/PMC3194693