Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tejaswini Waghmare"'
Autor:
Arnav Tongaonkar, Archana Sonawale, Daksha Prabhat, Tejaswini Waghmare, Alhad Mulkalwar, Maurya Patel
Publikováno v:
National Journal of Laboratory Medicine, Vol 12, Iss 2, Pp PC04-PC06 (2023)
Although eosinophilia is a recognised associated feature of Hodgkin’s Lymphoma, hypereosinophilia is seldom the presenting feature in the patient. Here, the authors report an unusual case of a 21-year-old male patient who presented to the General
Externí odkaz:
https://doaj.org/article/1fae2b2edc034b28b91c22105dc8e77c
Autor:
Tejaswini Waghmare, Pradeep Vaideeswar
Publikováno v:
Tropical Cardiovascular Pathology ISBN: 9789811937194
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a84dd0090ea07a84290a7ca9437677d4
https://doi.org/10.1007/978-981-19-3720-0_52
https://doi.org/10.1007/978-981-19-3720-0_52
Autor:
Pradeep Vaideeswar, Tejaswini Waghmare
Publikováno v:
Tropical Cardiovascular Pathology ISBN: 9789811937194
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03615d406060cb362f41fed8b6f71a07
https://doi.org/10.1007/978-981-19-3720-0_45
https://doi.org/10.1007/978-981-19-3720-0_45
Autor:
Tejaswini Waghmare, Pradeep Vaideeswar
Publikováno v:
Tropical Cardiovascular Pathology ISBN: 9789811937194
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9b18a4150a51af03a2b996ede7116bd
https://doi.org/10.1007/978-981-19-3720-0_7
https://doi.org/10.1007/978-981-19-3720-0_7
Publikováno v:
Annals of Pathology and Laboratory Medicine. 6:C83-87
Schwannomas are common benign neurogenic tumours that arise from Schwann cells of nerve roots; up to 45% arise in head and neck. However primary thyroid schwannomas are extremely rare. Among thyroid tumours papillary carcinoma of thyroid (PCT) are th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7cbf140e47fe7d08f2d401392f89d62c
https://doi.org/10.21276/apalm.2401
https://doi.org/10.21276/apalm.2401
Publikováno v:
Annals of Pathology and Laboratory Medicine. 6:A309-319
Background: Over the past five decades, hematology analyzers have evolved from semi-automated to fully automated ones. A histogram is a graphic representationof a collection of data based on cell size and/or cell number depicting variations in the pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2eaac376072f01f4798fd1d0acb52648
https://doi.org/10.21276/apalm.2527
https://doi.org/10.21276/apalm.2527
Publikováno v:
Annals of Pathology and Laboratory Medicine. 6:A103-111
Background: Leucoerythroblastic Reaction (LER) is defined as the presence of immature red cells and immature white cells of the myeloid series in peripheral blood. Literature has revealed various causes for LER, which include hemolyticanemia, infecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3808260f9a944182803b06509a8cbb8a
https://doi.org/10.21276/apalm.2410
https://doi.org/10.21276/apalm.2410
Publikováno v:
Diagnostic Cytopathology. 49
Kimura disease (KD) is a rare, idiopathic chronic inflammatory disorder that usually presents as unilateral painless lymphadenopathy or soft tissue swelling of the head and neck region in young Asian males. The disease lacks pathognomonic clinical an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dcb60c5b0ec3d3c0a29109a8b14f97d
https://doi.org/10.1002/dc.24658
https://doi.org/10.1002/dc.24658
Publikováno v:
International Journal of Research in Medical Sciences. 7:1079
Background: Hematolymphoid malignancies (HLM) are primary cancers of blood, bone marrow and lymphoid organs associated with high mortality. Clinically undetected cases, diagnosed primarily at autopsy, are common.Methods: Cases of HLMs at autopsy perf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::706e111bf05122a2cc704a72bd85982c
https://doi.org/10.18203/2320-6012.ijrms20191080
https://doi.org/10.18203/2320-6012.ijrms20191080
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 11, Pp ED23-ED24 (2016)
Holoprosencephaly is a rare congenital disorder which results from failure of cleavage or incomplete differentiation of the forebrain structures at various levels or to various degrees. Depending on the degree of involvement, it is classified into 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6d78437dbb0a725dffd5ea202d0005c
https://doi.org/10.7860/jcdr/2016/22453.8932
https://doi.org/10.7860/jcdr/2016/22453.8932