Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Somanath Padhi"'
Autor:
Jitendra Sharan, Sonali Mohapatra, Gaurav Chhabra, Somanath Padhi, Sandhya Biswal, Uday Hemant Barhate, Ashok Kumar Jena
Publikováno v:
Journal of Indian Society of Periodontology, Vol 27, Iss 2, Pp 201-206 (2023)
Various systemic diseases can manifest oral signs and symptoms early, which may be crucial for diagnosis and outlining the treatment plan. This case report highlights the presentation of acute leukemia (a malignancy of white blood cells) in a young f
Externí odkaz:
https://doaj.org/article/01eb23d2bbe64400beb8ac45665c5775
Autor:
Somanath Padhi, Rajlaxmi Sarangi
Publikováno v:
Journal of Current Research in Scientific Medicine, Vol 4, Iss 2, Pp 73-77 (2018)
Externí odkaz:
https://doaj.org/article/afc02c8125284fdeb97eed36547769d4
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 21, Iss 5, Pp 330-336 (2015)
Background /Aim: Narrow band imaging (NBI) is a novel, innovative high-resolution endoscopic technique, which utilizes spectral narrow band filter for the visualization of mucosal patterns and microvasculature. Nonerosive reflux disease (NERD) is a t
Externí odkaz:
https://doaj.org/article/466282e292224acd926c90566c43844e
Autor:
Somanath Padhi, Kandasamy Ravichandran, Jayaprakash Sahoo, Renu G'Boy Varghese, Aneesh Basheer
Publikováno v:
Lung India, Vol 32, Iss 6, Pp 593-601 (2015)
Background: Hemophagocytic lymphohistiocytosis (HLH) is an uncommon, potentially fatal, hyperinflammatory syndrome that may rarely complicate the clinical course of disseminated Mycobacterium tuberculosis (MTB). The clinical course of tuberculosis-as
Externí odkaz:
https://doaj.org/article/80a222eaf2bb4ed1b212b238e055194a
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 5, Pp ED15-ED17 (2017)
Overall incidence of primary cardiac tumour ranges from 0.0017% and 0.27% at autopsy. Cardiac haemangiomas are rare, and account for 2.8% of benign cardiac tumours. Pericardial haemangiomas, in particular are extremely rare. Pericardial haemangiomas
Externí odkaz:
https://doaj.org/article/bbce5e9ceb8f4bee94405ecd1e43f07e
Publikováno v:
Urology Annals, Vol 6, Iss 3, Pp 252-256 (2014)
Several case series, in the recent past, have postulated an association between plasma cell myeloma (MM) and renal cell carcinoma (RCC). Population-based data have revealed a bi-directional association between these two malignancies, which points to
Externí odkaz:
https://doaj.org/article/74231ba2aa884616b5f89e746de550b2
Publikováno v:
Iranian Journal of Medical Sciences, Vol 38, Iss 2(1), Pp 198-201 (2013)
Deficiency of vitamin B12 and/or folic acid as a cause of pyrexia, though known, is rarely reported in literature. We aimed to report a case in a 51 year old woman, who presented with fever and pancytopenia and was diagnosed to have megaloblastic ane
Externí odkaz:
https://doaj.org/article/f17b441625a84f0195b877c3b577b966
Autor:
Somanath Padhi, RajLaxmi Sarangi, Anita Ramdas, Kandasamy Ravichandran, Renu G’Boy Varghese, Thomas Alexander, George Kurien, Sudhagar Mookkappan
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 8, Iss 0, Pp e2016021-e2016021 (2016)
Background: Cutaneous hyperpigmentation is an often overlooked clinical sign in megaloblastic anemia (MA) which has been sporadically reported in the literature. Methods: We describe the bone marrow (BM) changes and clinicolaboaratory characteristic
Externí odkaz:
https://doaj.org/article/92a6fff9394e4d959edae246e06b3625
Autor:
Somanath Padhi, Tara Roshni Paul, Rajlaxmi Sarangi, Shantveer Uppin, Sundaram Challa, Putcha Deekshanti Narayan
Publikováno v:
Türk Nöroloji Dergisi, Vol 17, Iss 2, Pp 110-118 (2011)
Polyneuropathy (P), organomegaly (O), endocrinopathy (E), monoclonal gammopathy (M), and skin changes(S) (POEMS) syndrome is a rare multisystemic disease that occurs in the setting of plasma cell dyscrasia. Several hundred cases have been reported in
Externí odkaz:
https://doaj.org/article/976510f48bdd403b9273e1c1adeea6a2
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 3, Pp 127-129 (2014)
Sertoli Leydig Cell Tumours (SLCTs) are rare, unilateral, sex cord stromal tumours of ovary, which constitute less than 1% of all the ovarian neoplasms. These tumours can be functionally diverse and they may have heterologous elements. We aim to rep
Externí odkaz:
https://doaj.org/article/1b51fe99df4442e2bee18a07f6f2d203