Zobrazeno 1 - 10
of 160
pro vyhledávání: '"Pallewatte AS"'
Autor:
Lakmal, Tharange, Lamabadusuriya, Manuja, Satharasinghe, Duminda, Thilakshika, Rasuni, Pallewatte, Aruna, Jeyasugiththan, Jeyasingam
Publikováno v:
In Radiation Physics and Chemistry February 2024 215
Publikováno v:
In Radiography January 2023 29(1):62-69
Autor:
Sanjeewani Jagoda, Duminda Subasinghe, Yugantha Adhikari, Aruna Pallewatte, Sivasuriya Sivaganesh
Publikováno v:
SAGE Open Medical Case Reports, Vol 11 (2023)
Gallbladder duplication is a rare anomaly of the biliary tree. Implications of misdiagnosis include unwarranted surgery and morbidity such as when liver resections are done suspecting cystic intraductal papillary neoplasm of the bile duct. The use of
Externí odkaz:
https://doaj.org/article/38c0fc0033ff4a0fbb504b72c21225b1
Autor:
Satharasinghe, Duminda, Jeyasugiththan, Jeyasingam, Wanninayake, W.M.N.M.B., Pallewatte, A.S., Samarasinghe, R.A.N.K.K.
Publikováno v:
In Physica Medica October 2022 102:55-65
Autor:
Ranasinghe, Forensic Odontologist Dr. Sisira, Perera, Professor of Forensic Medicine and Toxicology Professor Jean, Taylor, Professor of Oral Biology Professor Jane A., Tennakoon, Forensic Pathologist Dr. Ajith, Pallewatte, Consultant Radiologist Dr. Aruna, Jayasinghe, Professor of Oral Medicine Professor Ruwan
Publikováno v:
In Forensic Imaging September 2022 30
Autor:
Bandara, Muditha S, Gurunayaka, Buddika, Lakraj, Gamage, Pallewatte, Aruna, Siribaddana, Sisira, Wansapura, Janaka
Publikováno v:
In Academic Radiology February 2022 29(2):229-235
Publikováno v:
Indian Journal of Radiology and Imaging, Vol 31, Iss 02, Pp 472-475 (2021)
Fibrolipomatous hamartoma is a rare nonhereditary, congenital condition characterized by benign hyperplasia of fibroadipose tissue around nerve bundles. The median nerve is commonly affected. Underlying pathological process is mature adipose and fibr
Externí odkaz:
https://doaj.org/article/2d459590143b49b6a2f6edd375f54684
Autor:
N. C. Pallewatte
Publikováno v:
Journal of the College of Community Physicians, Vol 28, Iss 1 (2022)
No abstract available
Externí odkaz:
https://doaj.org/article/3dd71b040ccc4c909ef3efa4e76e08a9
Autor:
Liyanage, Udari Apsara, Mathangasinghe, Yasith, Wijerathne, Pradeep Kumara, Vithoosan, Sahathevan, Pallewatte, Aruna
Publikováno v:
In Journal of Medical Imaging and Radiation Sciences September 2020 51(3):411-416
Publikováno v:
Sri Lanka Journal of Diabetes Endocrinology and Metabolism, Vol 9, Iss 2, Pp 44-48 (2019)
Congenital adrenal hyperplasia (CAH) is a group of inherited autosomal recessive disorders characterized by a defect in enzymes involved in biosynthesis of cortisol, aldosterone or both. We report two patients presented with recurrent haematuria with
Externí odkaz:
https://doaj.org/article/25c76d56c9614ac4a062c74c44aa9c29