Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Akshay Bali"'
Autor:
Maitrayee Roy, Akshay Bali
Publikováno v:
Journal of Laboratory Physicians, Vol 11, Iss 02, Pp 103-106 (2019)
BACKGROUND: Automated hematology analyzers often generate many flags which can provide important clues to the underlying hematological abnormality. Although pathologists are generally well versed in recognizing the importance of flags indicating pote
Externí odkaz:
https://doaj.org/article/9634870dcf4b4844a5b4308c79f49bd1
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 56, Iss 1, Pp 16-19 (2013)
Background: The increasing prevalence of multiple co-morbidities among anemic patients with chronic diseases have made the use of serum ferritin (which is also an acute phase reactant) and transferrin saturation more challenging in diagnosing iron de
Externí odkaz:
https://doaj.org/article/a647710621f340dc96e903f2ae15c18f
Publikováno v:
Indian Dermatology Online Journal, Vol 4, Iss 3, Pp 188-190 (2013)
Primary cutaneous leiomyosarcoma (PCL) is an exceedingly uncommon malignant superficial soft tissue sarcoma with a predilection for middle-aged to elderly male. Morphologic differential diagnosis includes a host of other malignant spindle cell neopla
Externí odkaz:
https://doaj.org/article/67e00526457449c8874ffbfc680c8a8a
Publikováno v:
Journal of Laboratory Physicians, Vol 4, Iss 01, Pp 053-055 (2012)
Clear cell sarcoma is a deep-seated, exceedingly rare aggressive tumor, typically involving the tendons and aponeuroses with melanocytic differentiation and a distinct genetic background. A primary dermal location is rarer. It exhibits histological,
Externí odkaz:
https://doaj.org/article/b9264515666e4b30b8d5af4a4ae1130d
Publikováno v:
Medical Journal Armed Forces India. 71:S181-S183
Polycystic kidney disease (PKD) is a hereditary disorder of autosomal dominant or recessive inheritance. Horseshoe kidney is a common renal fusion anomaly during embryogenesis. Combination of both PKD and horseshoe kidney is rare, with an incidence o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c37f5e556622d727a7cee7b2e2b41f2d
https://doi.org/10.1016/j.mjafi.2013.12.002
https://doi.org/10.1016/j.mjafi.2013.12.002
Publikováno v:
Journal of Cancer Research and Therapeutics, Vol 10, Iss 2, Pp 374-376 (2014)
Acantholytic variant of penile squamous cell carcinoma (SCC) is an exceedingly rare and associated with bad prognosis. Histologically it mimics angiosarcoma due to pseudovascular spaces. Vimentin immunopositivity in such cases represent epithelial to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54a2783f4e2d5757a163915043685acf
http://www.cancerjournal.net/article.asp?issn=0973-1482
http://www.cancerjournal.net/article.asp?issn=0973-1482
Autor:
Prakash R Malur, Akshay Bali, Maitrayee Roy, Rajeshwari Satish Handigund, Annasaheb J. Dhumale, Suvarna Inumella
Acute leukemia, secondary myelodysplasia and paroxysmal nocturnal hemoglobinuria evolving from severe aplastic anemia (AA) following immunosuppressive therapy are well recognized. However, severe AA occurring after complete remission of acute promyel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6756b714af0ce4eb8bb53f6413158fc
https://europepmc.org/articles/PMC3921322/
https://europepmc.org/articles/PMC3921322/
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 56, Iss 1, Pp 16-19 (2013)
Background: The increasing prevalence of multiple co-morbidities among anemic patients with chronic diseases have made the use of serum ferritin (which is also an acute phase reactant) and transferrin saturation more challenging in diagnosing iron de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f28849940947b9da05e771e0d3ebd549
https://doi.org/10.4103/0377-4929.116142
https://doi.org/10.4103/0377-4929.116142
Publikováno v:
Journal of Dr. NTR University of Health Sciences. 2:130
Congenital diaphragmatic hernia (CDH) is a common congenital anomaly that frequently occurs in conjunction with other major anomalies, including chromosomal abnormalities. Fryns syndrome (FS) is a lethal syndrome that most frequently features CDH as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1179177713eb61e7d3c01a33fb7d90b8
https://doi.org/10.4103/2277-8632.112346
https://doi.org/10.4103/2277-8632.112346
Publikováno v:
Indian Journal of Dermatology, Venereology and Leprology, Vol 78, Iss 4, Pp 494-496 (2012)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6e95d8f33c4de40c1c942d67b56ef04
https://doi.org/10.4103/0378-6323.98085
https://doi.org/10.4103/0378-6323.98085