Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Radheshyam, Purkait"'
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 17, Iss 5, Pp 943-950 (2024)
Background and Aims: Despite contemporary discussion on the clinical presentation, imaging studies, indications of appendicectomy, and the best available approach, a diagnostic delay due to atypical presentations of appendicitis in preschool children
Externí odkaz:
https://doaj.org/article/14d48434620c417293f3c244cacbf865
Publikováno v:
Asian Journal of Medical Sciences, Vol 14, Iss 4, Pp 185-191 (2023)
Background: Scrub Typhus, a Rickettsial disease is an emerging tropical disease mainly in South East Asia. Very few studies are there in pediatric age group and mainly limited to epidemiological and clinical profile only. Aims and Objectives: The
Externí odkaz:
https://doaj.org/article/3ec21b8830634869a111e5fa7ca58945
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 24, Iss 2, Pp 129-135 (2023)
Objectives: To identify the spectrum of cutaneous manifestations and to evaluate temporal relationship between each type of dermatological lesions and the severity of COVID-19-related illness in the pediatric population. Subjects and Methods: Retrosp
Externí odkaz:
https://doaj.org/article/ebc9e9f7d8f640bc88d1e13aa1fe9bc8
Autor:
Tryambak Samanta, Rajarshi Basu, Radheshyam Purkait, Sudipta Kar, Debasis Das, Sutapa Ganguly
Publikováno v:
JGH Open, Vol 5, Iss 1, Pp 20-27 (2021)
Abstract Background and Aim Limited data exist regarding the etiological spectrum of the subset of chronic liver diseases (CLDs) diagnosed in noncirrhotic states in children. Our primary objective was to study the clinicoetiological profile of CLDs d
Externí odkaz:
https://doaj.org/article/0cefad10177a41798668c06bfe7abb2b
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 26, Iss 4, Pp 778-782 (2015)
A 9-year-old girl, diagnosed case of Fanconi anemia, presented with generalized convulsion with altered sensorium. She had fever, severe pallor, sinus tachycardia, blood pressure of 180/120 mmHg in both upper and lower limb, pan-systolic murmur of gr
Externí odkaz:
https://doaj.org/article/dc3e4a1e7df4400cbc93ab72997665e3
Autor:
Radheshyam Purkait, Saubhik Ghosh, Kalidas Biswas, Manoj Gupta, Rajarshi Basu, Debasis Das, Shristi Butta, Tryambak Samanta, Abhisek Naskar, Sutapa Ganguly
Publikováno v:
Clinical and Experimental Gastroenterology. 13:503-509
Background Baveno VI criteria for screening varices needing treatment (VNT) have not yet been validated in an exclusive pediatric and adolescent set of the population, in whom baseline parameters differ in relation to adults. Therefore, our primary o
Autor:
Tryambak Samanta, Debasis Das, Radheshyam Purkait, Sutapa Ganguly, Sudipta Kar, Rajarshi Basu
Publikováno v:
JGH Open, Vol 5, Iss 1, Pp 20-27 (2021)
JGH Open: An Open Access Journal of Gastroenterology and Hepatology
JGH Open: An Open Access Journal of Gastroenterology and Hepatology
Background and Aim Limited data exist regarding the etiological spectrum of the subset of chronic liver diseases (CLDs) diagnosed in noncirrhotic states in children. Our primary objective was to study the clinicoetiological profile of CLDs detected i
Publikováno v:
Indian Journal of Dermatology, Vol 56, Iss 4, Pp 375-379 (2011)
Background: Neurocutaneous syndromes (NCS) are a group of genetic disorders that produce a variety of developmental abnormalities of the skin along with an increased risk of neurological complications. Cutaneous manifestations usually appear early in
Externí odkaz:
https://doaj.org/article/034e217431944825a8da2cd525ba7ab1
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 19, Iss 3, Pp 175-177 (2014)
Medium chain triglyceride (MCT)-based diet, total parenteral nutrition (TPN) and repeated paracentesis are considered as supportive management for congenital chylous ascites (CCA). TPN is considered where therapy with oral MCT is poorly tolerated by
Externí odkaz:
https://doaj.org/article/66c8a0ad5605499598467bd40aa59498
Publikováno v:
Annals of Indian Academy of Neurology, Vol 16, Iss 2, Pp 289-291 (2013)
Varadi Papp syndrome or oral-facial-digital syndrome type VI (OFDS VI) is a rare autosomal-recessive disorder distinguished from other OFDSs by metacarpal abnormalities with central polydactyly and by cerebellar abnormalities. Our patient had a broad
Externí odkaz:
https://doaj.org/article/b2c85f3ffd444d58be40c81b33c23d10