Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Appalanaidu, Sasapu"'
Autor:
Shebli Atrash, MD, Appalanaidu Sasapu, MD, Soumya Pandey, MD, Michele Cottler-Fox, MD, Pooja Motwani, MD
Publikováno v:
Mayo Clinic Proceedings: Innovations, Quality & Outcomes, Vol 2, Iss 1, Pp 69-73 (2018)
Objective: To explore the benefits of adding eculizumab for the treatment of refractory autoimmune thrombotic thrombocytopenic purpura (iTTP) with complement dysregulation. Patients and Methods: From January 1, 2014, through July 1, 2017, we identifi
Externí odkaz:
https://doaj.org/article/4bf4c1e4e9124c1f9581de3842c251f1
Publikováno v:
Avicenna Journal of Medicine, Vol 07, Iss 03, Pp 133-136 (2017)
Chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) is a B-cell lymphocytic neoplasm with indolent clinical course. If identified early, observation is opted. Many variables lead to the initiation of treatment. Authors describe a 62-yea
Externí odkaz:
https://doaj.org/article/afe53fafc617425aa29efae42c663f21
Publikováno v:
Journal of Global Oncology, Vol 4, Pp 1-4 (2017)
Externí odkaz:
https://doaj.org/article/7906eec99ea74705bcbeacac9b72e96d
Autor:
Archana Hinduja, Kaustubh Limaye, Rahul Ravilla, Appalanaidu Sasapu, Xenofon Papanikolaou, Lai Wei, Michel Torbey, Sarah Waheed
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0175218 (2017)
[This corrects the article DOI: 10.1371/journal.pone.0166627.].
Externí odkaz:
https://doaj.org/article/533d4af8f11e4415bb6c52dc782bec83
Publikováno v:
Perm J
INTRODUCTION: Acquired hemophilia A (AHA) is a rare bleeding disorder caused by autoantibodies against clotting factor VIII. It occurs most commonly in the elderly population. AHA is associated with malignancy, autoimmune diseases, pregnancy, and dru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2d2412e9ee6bedf2c4ddde46e14f5d6
https://europepmc.org/articles/PMC9662262/
https://europepmc.org/articles/PMC9662262/
Autor:
Francisco Socola, Giovanni Insuasti-Beltran, Rodolfo Henrich Lobo, Shebli Atrash, Appalanaidu Sasapu
Publikováno v:
Case Reports in Oncological Medicine, Vol 2016 (2016)
We report the case of a young African American male with no significant past medical history presenting with low back and bilateral leg pain; presenting CBC and chemistries revealed elevated white blood cell count of 250,000, with anemia (Hb 6.8 g/dL
Externí odkaz:
https://doaj.org/article/77edf553402b4665aa587afb0f0ace6f
Autor:
Arya Mariam Roy, Manojna Konda, Appalanaidu Sasapu, Issam Makhoul, Yadav Pandey, Jacob Leffert
Publikováno v:
Journal of the National Comprehensive Cancer Network. 18:QIM20-131
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce17d4812cf2006660a5090a8fea5ef2
https://doi.org/10.6004/jnccn.2019.7487
https://doi.org/10.6004/jnccn.2019.7487
Autor:
Arya Mariam Roy, Appalanaidu Sasapu, Muthu Veeraputhiran, Yadav Pandey, Derek Middleton, Brannon Broadfoot
Publikováno v:
Cureus
Intravascular large B-cell lymphoma is a rare malignancy characterized by the presence of lymphoma cells within the lumen of blood vessels. The annual incidence of cases is fewer than 0.5 cases per 1,000,000. It usually affects the elderly with an av
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c16d334d8db36e5334844bc9250700e1
http://europepmc.org/articles/PMC8370572
http://europepmc.org/articles/PMC8370572
Publikováno v:
Anticancer research. 41(7)
Background Treatment of refractory/relapsing diffuse large B cell (R/R DLBCL) lymphoma remains a challenge. Radiation therapy (RT) has versatile roles in R/R DLBCL treatment: it can be used in the peri-transplant setting for transplant-eligible candi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62317aeb443eefcf9986e58d363f762a
https://pubmed.ncbi.nlm.nih.gov/34230160
https://pubmed.ncbi.nlm.nih.gov/34230160
Autor:
Belal Firwana, Milan Bimali, Dinesh Atwal, Manojna Konda, Appalanaidu Sasapu, Yadav Pandey, Derek Middleton, Naveen Yarlagadda
Publikováno v:
Proc (Bayl Univ Med Cent)
Hemophagocytic lymphohistiocytosis (HLH) is an underrecognized disorder due to the variability of its presentation and the fact that in adults, its diagnosis is based on cumbersome, pediatric-based criteria. Data regarding demographics, underlying ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b97361619d8a6dbb2936d3dd288a149b
https://europepmc.org/articles/PMC7340478/
https://europepmc.org/articles/PMC7340478/