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of 8
pro vyhledávání: '"Ashbita Pokharel"'
Autor:
Randhir Sagar Yadav, Ashik Pokharel, Deepshikha Gaire, Shumneva Shrestha, Ashbita Pokharel, Sumita Pradhan, Prasan Bir Singh Kansakar
Publikováno v:
Case Reports in Endocrinology, Vol 2021 (2021)
Multiple endocrine neoplasia type 1 (MEN1) is a rare syndrome of autosomal dominant inheritance defined by co-occurrence of two or more tumors originating from the parathyroid gland, pancreatic islet cells, and/or anterior pituitary. Insulinoma which
Externí odkaz:
https://doaj.org/article/fed34fcd93304f0fbb1c1b5f4a8adfd5
Autor:
Randhir Sagar Yadav, Ashik Pokharel, Shumneva Shrestha, Ashbita Pokharel, Deepshikha Gaire, Sumita Pradhan, Prasan Bir Singh Kansakar
Publikováno v:
Case Reports in Oncological Medicine, Vol 2021 (2021)
Mixed serous-neuroendocrine neoplasm constitutes pancreatic serous cystic neoplasms and pancreatic neuroendocrine tumor, two tumor components with different underlying pathologies. The differentiation of these tumors is important as the management an
Externí odkaz:
https://doaj.org/article/d61164f3d24c4d29ae6bc2fd7d6d9a42
Publikováno v:
Case Reports in Neurological Medicine, Vol 2017 (2017)
Background. Neuromyelitis optica is a severely disabling inflammatory disorder of the central nervous system of autoimmune etiology that mainly affects the optic nerves and spinal cord. Here, we present a case report detailing a patient with tingling
Externí odkaz:
https://doaj.org/article/eafe4f187a6d4b93a837c379dba53f98
Publikováno v:
Clinical Lung Cancer. 24:e113-e116
Background: Adult head and neck rhabdomyosarcoma (AHNRMS) is an exceedingly rare soft-tissue sarcoma. We describe a case of AHNRMS that was initially misdiagnosed as atypical fibroxanthoma (AFX). Methods: A 61-year-old male with a history of cutaneou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcf80d010b64cc123fa89f07492c64a7
https://doi.org/10.22541/au.166601152.26075962/v1
https://doi.org/10.22541/au.166601152.26075962/v1
Autor:
P. Kansakar, Sumita Pradhan, Ashbita Pokharel, Ashik Pokharel, Deepshikha Gaire, Shumneva Shrestha, Randhir Sagar Yadav
Publikováno v:
Case Reports in Endocrinology
Case Reports in Endocrinology, Vol 2021 (2021)
Case Reports in Endocrinology, Vol 2021 (2021)
Multiple endocrine neoplasia type 1 (MEN1) is a rare syndrome of autosomal dominant inheritance defined by co-occurrence of two or more tumors originating from the parathyroid gland, pancreatic islet cells, and/or anterior pituitary. Insulinoma which
Autor:
P. Kansakar, Ashik Pokharel, Randhir Sagar Yadav, Deepshikha Gaire, Sumita Pradhan, Ashbita Pokharel, Shumneva Shrestha
Publikováno v:
Case Reports in Oncological Medicine, Vol 2021 (2021)
Case Reports in Oncological Medicine
Case Reports in Oncological Medicine
Mixed serous-neuroendocrine neoplasm constitutes pancreatic serous cystic neoplasms and pancreatic neuroendocrine tumor, two tumor components with different underlying pathologies. The differentiation of these tumors is important as the management an
Publikováno v:
Case Reports in Neurological Medicine, Vol 2017 (2017)
Case Reports in Neurological Medicine
Case Reports in Neurological Medicine
Background. Neuromyelitis optica is a severely disabling inflammatory disorder of the central nervous system of autoimmune etiology that mainly affects the optic nerves and spinal cord. Here, we present a case report detailing a patient with tingling