Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kamala Manogna Nibhanupudi"'
Autor:
Vasanthapriya Janarthanan, Thara Keloth, Joe Vimal Raj, Roshen Raghaventhar Raghuraman, Elamparidhi Padmanaban, Kamala Manogna Nibhanupudi
Publikováno v:
International Journal of Anatomy Radiology and Surgery, Vol 13, Iss 04, Pp 01-04 (2024)
Introduction: Radiological imaging, such as High-resolution Computed Tomography (HRCT) of the temporal bone, has always held significant importance in diagnosing and staging Chronic Suppurative Otitis Media (CSOM). In preoperative cases of CSOM and c
Externí odkaz:
https://doaj.org/article/0223df412f554c75896d5689e84aa84c
Autor:
Kamala Manogna Nibhanupudi, Monika Gangapatnam, Elamparidhi Padmanaban, Umamageswari Amirthalingam, Joe Vimal Raj, M. Bharathi
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 55, Iss 1, Pp 1-8 (2024)
Abstract Background Adenoid cystic carcinoma is an uncommon malignancy primarily arising from salivary glands. An extremely rare site for adenoid cystic carcinoma is the skull base. We report a case of adenoid cystic carcinoma of skull base who prese
Externí odkaz:
https://doaj.org/article/39d52d9a1ef74d1490d0e6418f0a4912
Autor:
Kamala Manogna Nibhanupudi, Monika Gangapatnam, Elamparidhi Padmanaban, Umamageswari Amirthalingam, Joe Vimal Raj, M. Bharathi
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 55, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/3b1ee8a51d4c4b148ab617e87ead6c6f
Autor:
Elamparidhi Padmanaban, Kamala Manogna Nibhanupudi, Umamageswari Amirthalingam, Padma Rekha, Rintu George
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 52, Iss 1, Pp 1-7 (2021)
Abstract Background Congenital cystic adenomatoid malformation is an uncommon developmental anomaly that is diagnosed prenatally or during early childhood and is rare to present in adulthood. Type 2 congenital cystic adenomatoid malformation is often
Externí odkaz:
https://doaj.org/article/be25761d27144662a7440a419f15cd7e
Autor:
Rintu George, Elamparidhi Padmanaban, Padma Rekha, Kamala Manogna Nibhanupudi, Umamageswari Amirthalingam
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 52, Iss 1, Pp 1-7 (2021)
Background Congenital cystic adenomatoid malformation is an uncommon developmental anomaly that is diagnosed prenatally or during early childhood and is rare to present in adulthood. Type 2 congenital cystic adenomatoid malformation is often associat