Zobrazeno 1 - 10
of 224
pro vyhledávání: '"Robert S, Ohgami"'
Autor:
Punit Jain, Poonam Jain, Robert S. Ohgami, Veena Pawar, Kunal Sehgal, Pradnya Chaudhari, Ravindra Nikalji, Tejinder Singh, Vipin Khandelwal, Sanjay Khare, Vaishali Lokhande, Ashwathy Haridas, Laxman Jessani, Kanika Khandelwal
Publikováno v:
eJHaem, Vol 5, Iss 1, Pp 251-255 (2024)
Abstract Primary renal involvement by T lymphoblasts is rare among adults with T acute lymphoblastic leukaemia. We report a 28‐year‐old man presenting with acute renal failure due to infiltration by T lymphoblasts and his response to paediatric
Externí odkaz:
https://doaj.org/article/fb2a4533e9ab4efba1a634ed819ed01c
Autor:
Andrew Xiao, Nahid Shahmarvand, Alexandra Nagy, Jyoti Kumar, Jessica Van Ziffle, Patrick Devine, Franklin Huang, Lhara Lezama, Peng Li, Robert S. Ohgami
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Anaplastic lymphoma kinase (ALK) positive large B-cell lymphoma (ALK+ LBCL) is an aggressive and rare subtype of B-cell lymphoma. Patients typically present with advanced clinical stage disease and do not respond to conventional chemotherapy; the med
Externí odkaz:
https://doaj.org/article/03c6998d8089436e9c52ba034407c755
Autor:
Kunwar I. Singh, Sumanth Gollapudi, Jyoti Kumar, Alexandra Butzmann, Corinn Small, Sara Kreimer, Emine Arzu Saglam, Roger Warnke, Oscar Silva, Robert S. Ohgami
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Castleman disease (CD) is a rare lymphoproliferative disorder with distinct clinical subtypes. However, our understanding of the underlying pathogenesis of particular subtypes of CD remains unclear. While the characteristic morphologic changes within
Externí odkaz:
https://doaj.org/article/a3a71a25359547c687327d71a47fc144
Mutations in JAK/STAT and NOTCH1 Genes Are Enriched in Post-Transplant Lymphoproliferative Disorders
Autor:
Alexandra Butzmann, Kaushik Sridhar, Diwash Jangam, Hanbing Song, Amol Singh, Jyoti Kumar, Karen M. Chisholm, Benjamin Pinsky, Franklin Huang, Robert S. Ohgami
Publikováno v:
Frontiers in Oncology, Vol 11 (2022)
Post-transplant lymphoproliferative disorders (PTLD) are diseases occurring in immunocompromised patients after hematopoietic stem cell transplantation (HCT) or solid organ transplantation (SOT). Although PTLD occurs rarely, it may be associated with
Externí odkaz:
https://doaj.org/article/16330ea7f6f941179cf86195dd2203b7
Publikováno v:
Diagnostic Histopathology. 29:237-245
Autor:
Jyoti Kumar, Samit Patel, Abraham Chang, Soham Mukherjee, Corinn Small, Sumanth Gollapudi, Alexandra Butzmann, Diwash Jangam, Olga K. Weinberg, Tracy I. George, James L. Zehnder, Robert S. Ohgami
Publikováno v:
Human Pathology. 135:45-53
Autor:
Alexandra Nagy, Aparna Bhaduri, Nahid Shahmarvand, Jahanbanoo Shahryari, James L. Zehnder, Roger A. Warnke, Tariq Mughal, Siraj Ali, Robert S. Ohgami
Publikováno v:
Blood Advances, Vol 2, Iss 5, Pp 481-491 (2018)
Abstract: Castleman disease (CD) is a rare lymphoproliferative disorder subclassified as unicentric CD (UCD) or multicentric CD (MCD) based on clinical features and the distribution of enlarged lymph nodes with characteristic histopathology. MCD can
Externí odkaz:
https://doaj.org/article/ed23b9e6ab5f434f8db458b54d327323
Autor:
Kevin L. Lu, Joshua R. Menke, David Ng, Roberto Ruiz-Cordero, Amanda Marinoff, Elliot Stieglitz, Sumanth Gollapudi, Kunwar Singh, Robert S. Ohgami, Poonam Vohra
Publikováno v:
Journal of the American Society of Cytopathology. 11:281-294
Pediatric-type follicular lymphoma (PTFL) is a rare and recently recognized subtype of nodal follicular B-cell lymphoma. While significant recent progress has been made in understanding the morphologic, immunophenotypic, and molecular findings, there
Autor:
Lhara Lezama, Robert S. Ohgami
Publikováno v:
Haematologica, Vol 104, Iss 4 (2019)
Externí odkaz:
https://doaj.org/article/747a92a50db94543b7ae1dd4bdfb5fdd
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Gain-of-function variants in p110δ, the catalytic subunit of phosphatidylinositol 3-kinase (PI3K) expressed in lymphocytes, cause activated PI3-kinase δ syndrome (APDS), a primary immunodeficiency that is characterized by recurrent infections, vire
Externí odkaz:
https://doaj.org/article/76a5fb0566f14f57964c35dcc41b6e8b