Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Gita R, Bhat"'
Publikováno v:
Asian Journal of Oncology, Vol 03, Iss 01, Pp 087-091 (2017)
De novo (pretreatment) epidermal growth factor receptor T790M mutation in non-small-cell lung cancer (NSCLC) is rare when detected by standard genotyping methods. We present a case of concurrent de novo T790M and L858R mutations detected by direct se
Externí odkaz:
https://doaj.org/article/7c8d26995d7a424890d8bd8dc9f00a28
Publikováno v:
Case Reports in Oncological Medicine, Vol 2016 (2016)
Background. Acute promyelocytic leukemia is characterized by t(15;17). This leads to the formation of PML/RARα which blocks the differentiation of blasts at the stage of promyelocytes. This is reversed by all-trans-retinoic acid (ATRA), a vitamin A
Externí odkaz:
https://doaj.org/article/08d4874b0ed64210ae0ef750a30ea34e
Publikováno v:
Asian Journal of Oncology, Vol 03, Iss 01, Pp 087-091 (2017)
De novo (pretreatment) epidermal growth factor receptor T790M mutation in non-small-cell lung cancer (NSCLC) is rare when detected by standard genotyping methods. We present a case of concurrent de novo T790M and L858R mutations detected by direct se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b182cfe93d83c3c98077c84bc05679d3
https://doi.org/10.4103/2454-6798.209336
https://doi.org/10.4103/2454-6798.209336
Autor:
L Appaji, B S Aruna Kumari, K Govind Babu, C S Premalata, K. P. R. Pramod, Gita R Bhat, Chinchu Prem
Publikováno v:
Journal of Cancer Research and Therapeutics, Vol 13, Iss 6, Pp 1015-1022 (2017)
Background: Atypical teratoid rhabdoid tumors (AT/RT) constitute a rare group of pediatric brain tumors. Aim: To study the clinical, histopathological, and immunohistochemical (IHC) profile, management and outcome of children with AT/RT of the centra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::b0711b049009e820e10766c536764418
http://www.cancerjournal.net/article.asp?issn=0973-1482
http://www.cancerjournal.net/article.asp?issn=0973-1482
Autor:
B.G. Sumati, B.R. Vijaykumar, Harsha Vardhana, R. S. Jayshree, Mahua Sinha, K Govind Babu, K C Lakshmaiah, Gita R Bhat, D. Lokanatha, M C Suresh Babu, Linu Abraham Jacob
Publikováno v:
Indian Journal of Medical and Paediatric Oncology : Official Journal of Indian Society of Medical & Paediatric Oncology
Introduction: Febrile neutropenia (FN) is an oncological emergency. The choice of empiric therapy depends on the locally prevalent pathogens and their sensitivities, the sites of infection, and cost. The Infectious Diseases Society of America guideli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::636bc7b7d0c99663668bb23069377ebd
https://doi.org/10.4103/0971-5851.190352
https://doi.org/10.4103/0971-5851.190352
Publikováno v:
Indian Journal of Medical and Paediatric Oncology : Official Journal of Indian Society of Medical & Paediatric Oncology
Introduction: Prolonged treatment, frequent administration of chemotherapy, antibiotics and blood products in cancer patients requires long term venous access. Central venous catheters (CVC) inserted into the subclavian vein or internal jugular vein,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b63cef48bdcf38a3dbaf1f4009316e2
http://europepmc.org/articles/PMC5234158
http://europepmc.org/articles/PMC5234158
Publikováno v:
OALib. :1-8
Cancer survivors are faced with several survivorship issues. In addition, young women may have to face the challenges brought on by premature menopause. The issue of Hormone Replacement Therapy (HRT) in these young ladies has always been a matter of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71ffcde3ea6eebb36a31f45973376298
https://doi.org/10.4236/oalib.1102069
https://doi.org/10.4236/oalib.1102069
Autor:
K Govind Babu, Gita R Bhat
Publikováno v:
ecancermedicalscience
Cancer-associated thrombotic microangiopathy refers to a group of disorders characterised by microvascular thrombosis, thrombocytopenia, and ischaemic end-organ damage. Haemolytic uraemic syndrome and thrombotic thrombocytopenic purpura are the two m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28cbf3e7c277c36012ef463bfa281286
https://pubmed.ncbi.nlm.nih.gov/27433282
https://pubmed.ncbi.nlm.nih.gov/27433282
Publikováno v:
West African Journal of Radiology. 24:76
Background: Malignant infantile osteopetrosis (MIOP) is an autosomal recessive disorder which is characterized by densely sclerotic bone due to defective function of osteoclasts. Overgrowth of bone results in nerve compression and reduction of marrow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88578662a7a46f1cb9aace461452e8be
https://doi.org/10.4103/1115-3474.192754
https://doi.org/10.4103/1115-3474.192754