Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Humaira, Nasir"'
Publikováno v:
Journal of the Pakistan Medical Association, Vol 73, Iss 9 (2023)
Extra-neural metastases of glioblastoma multiforme are uncommon with unidentified metastatic mechanism. There is no consensus over optimum treatment regimen. The current narrative review was planned to illuminate the presence criteria, sites of metas
Externí odkaz:
https://doaj.org/article/bd9a6a93bad64d59bec57d82d27d52fb
Publikováno v:
Journal of Rawalpindi Medical College, Vol 26, Iss 4 (2022)
Objectives: Obstructed labour is an obstetrical emergency with adverse feto-maternal consequences and caesarean delivery in such cases requires skillful handling of impacted fetal head. Objective of our study was to guide clinician about caesarean
Externí odkaz:
https://doaj.org/article/2d5c7f6192474637896487705ac42919
Autor:
Nadira Mamoon, Hania Naveed, Mariam Abid, Humaira Nasir, Imran Nazir Ahmad, Zujajah Hameed, Asna Haroon Khan
Publikováno v:
Journal of the Pakistan Medical Association, Vol 71, Iss 2 (2020)
Objective: Clinicopathological features of gastroenteropancreatic neuroendocrine tumors (GEP-NETs) have rarely been studied in the Pakistani population. We investigated the clinical characteristics of these tumors according to the updated World Healt
Externí odkaz:
https://doaj.org/article/80af387170984468a14b57f781e9d5ea
Publikováno v:
Journal of Cancer and Allied Specialties, Vol 4, Iss 1 (2018)
Objective: The objective of this study was to evaluate the effectiveness of intradepartmental consultation conference (IDC) as a good quality control measure and problem-solving activity in a busy histopathology department. Methods: This study was d
Externí odkaz:
https://doaj.org/article/425ee706d93c404ba0cb530cf40b6c15
Publikováno v:
American Journal of Medical Case Reports. 9:693-697
Karyomegalic interstitial nephritis (KIN) is a rare cause of hereditary interstitial nephritis, described 45 years ago. Only about 50 cases have been described in English literature so far and none from Pakistan. This disease has an escalated course
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10e1d2783303cc677db297325136e716
https://doi.org/10.12691/ajmcr-9-12-8
https://doi.org/10.12691/ajmcr-9-12-8
Autor:
Asim Qureshi, Hina Tariq, Zafar Ali, Nadira Mamoon, Imran N Ahmed, Asna H Khan, Humaira Nasir
Publikováno v:
Journal of Cancer and Allied Specialties, Vol 2, Iss 4 (2016)
Objective: The objective of this study was to determine the morphologic spectrum and risk category of gastrointestinal stromal tumour (GIST) and compare with overall patient survival. Materials and Methods: It is a descriptive observational study. T
Externí odkaz:
https://doaj.org/article/cdef4374ae0748b69a3704a44e0ae5c9
Autor:
Humaira Nasir, Khan Ah, Mariam Abid, Nadira Mamoon, Imran Ahmad, Zujajah Hameed, Hania Naveed
Publikováno v:
Journal of the Pakistan Medical Association. :1-14
Objective: Clinicopathological features of gastroenteropancreatic neuroendocrine tumors (GEP-NETs) have rarely been studied in the Pakistani population. We investigated the clinical characteristics of these tumors according to the updated World Healt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7701309d940e74907486cc85ace93d7
https://doi.org/10.47391/jpma.835
https://doi.org/10.47391/jpma.835
Publikováno v:
Cureus. 14(1)
Introduction Systemic amyloidosis can affect any organ in the body, but the kidney is the most commonly involved site. It is characterized by the extracellular deposition of insoluble fibrillar proteins. Amyloid deposits can be identified histologica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38744784f39fbcb121e095bc96164741
https://pubmed.ncbi.nlm.nih.gov/35165578
https://pubmed.ncbi.nlm.nih.gov/35165578
Publikováno v:
Cureus
Background Membranous nephropathy (MN) and immunoglobulin A nephropathy (IgAN) are although two different entities, yet can rarely coexist. There is not much data available on this coexistent disorder, specifically with regard to the treatment modali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8da76754cd36f770958663875b83d7b5
https://pubmed.ncbi.nlm.nih.gov/34667681
https://pubmed.ncbi.nlm.nih.gov/34667681
Publikováno v:
Cureus
Bartter syndrome is a rare autosomal recessive, salt-losing disorder characterized by hypokalemic hypochloremic metabolic alkalosis. We are reporting a case of 21 years old patient, who presented with lower limb weakness, marked hypokalemia, proteinu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f37de14f1ea8b46f85bc1d38005ad14e
http://europepmc.org/articles/PMC8435068
http://europepmc.org/articles/PMC8435068