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of 8 873
pro vyhledávání: '"11"'
Autor:
Carlos E. Bueso-Ramos, Yang O. Huh, L. Jeffrey Medeiros, Ali Sakhdari, Chi Young Ok, Zhenya Tang
Publikováno v:
Cancer Genetics. 238:18-22
AML and MDS are most common myeloid neoplasms that affect mainly older patients. Overexpression of certain proto-oncogenes plays an indispensable role in tumorigenesis and overexpression can be a consequence of gene rearrangement, amplification and/o
Autor:
Clara D. Bloomfield, Bayard L. Powell, Andrew J. Carroll, Shelley Orwick, Ann-Kathrin Eisfeld, Jessica Kohlschmidt, Bhavana Bhatnagar, Dimitrios Papaioannou, Richard Stone, Deedra Nicolet, Krzysztof Mrózek, John C. Byrd, Jonathan E. Kolitz, Christopher J. Walker, James S. Blachly
Publikováno v:
Leukemia. 34:358-368
Sole trisomies of chromosomes 4, 8, 11, 13 and 21 account for 89–95% of all sole trisomies in adult AML patients. We analyzed clinical and molecular characteristics of 138 de novo AML patients with sole +4, +8, +11, +13 or +21, and compared them wi
Autor:
Rick Szymialis, Nicole Glowacki, Kara Nitti, Rasha Khatib, Chris Blair, Marc McDowell, William Rhoades
Publikováno v:
Journal of Thrombosis and Thrombolysis
A gap exists between clinical practice guidelines and real-world practice. We aim to investigate hospital admissions among patients presenting to emergency departments of 11 hospitals with venous thromboembolism (VTE). Eligible patients’ first emer
Autor:
Jean-Etienne Castelain, Camille Damade, Romain Masse, Olivier Gille, Marion Petit, Soufiane Ghailane, Simon Mazas, Benjamin Bouyer, David C. Kieser
Publikováno v:
World Neurosurgery. 138:e305-e310
Objective To assess the efficacy and safety of surgery for dysphagia in anterior cervical idiopathic hyperostosis. Methods This retrospective study included 11 consecutive patients presenting with dysphagia and anterior cervical idiopathic hyperostos
Autor:
Keisuke Goto, Takuma Oishi, Masaru Tanaka, Kohei Ogawa, Keiichiro Honma, Yoji Kukita, Haruto Nishida, Toshihiro Takai, Taiki Isei, Tsunekazu Hishima
Publikováno v:
HistopathologyReferences. 79(6)
AIMS The aim of this study was to determine the clinicopathological and genetic characteristics of axillary signet-ring cell/histiocytoid carcinoma (SRCHC) and the relationship between axillary SRCHC, eyelid SRCHC, and conventional apocrine carcinoma
Autor:
Jinyoung Park
Publikováno v:
Medicine
Obturator hernia is a relatively rare type of abdominal hernia, in which abdominal contents protrude through the obturator canal, a condition that can lead to small bowel obstruction. Its rarity and nonspecific signs and symptoms make a preoperative
Autor:
Jan Konrad Siwicki, Michalina Zajdel, Jan Walewski, Magdalena Chechlinska, Barbara Pienkowska-Grela, Katarzyna Blachnio, Krzysztof Goryca, Grzegorz Rymkiewicz, Paweł Swoboda, Zbigniew Bystydzienski, Maria Cieslikowska, Beata Grygalewicz
Publikováno v:
Tumor Biology. 36:5377-5388
Fast and reliable differential diagnosis of Burkitt lymphoma (BL) vs. diffuse large B cell lymphoma (DLBCL) is of major importance for therapeutic decisions and patient outcome. Aggressive B cell non-Hodgkin lymphomas (B-NHLs) that do not belong to t
Autor:
Catherine Chung, Alejandro A. Gru, Melissa Pulitzer, Govind Bhagat, Shyam S. Raghavan, Antonio Subtil, Martin Sangueza, Jose A. Plaza
Publikováno v:
Am J Surg Pathol
Cutaneous anaplastic large cell lymphoma (C-ALCL) represents one of the entities within the group of CD30-positive lymphoproliferative disorders (LPDs) of the skin. Most cases are ALK-negative, though isolated cases of ALK-positive C-ALCL have also b
Autor:
Christopher Conklin, Avrum Ostry, Gang Wang, Chen Zhou, Edward C. Jones, Carlos F. Villamil, Malcolm Hayes
Publikováno v:
Virchows Archiv. 474:333-339
Metastatic breast carcinoma to the urinary bladder is rare. Eleven cases of metastatic breast carcinoma to the bladder are described in this report, including one case with a tumor to tumor metastasis. The patients ranged from 51 to 83 years of age.
Autor:
Noelia Sastre, Marta Alonso-Guervós, Ana Salas-Bustamante, David Hardisson, César Álvarez-Marcos, Andrés Sampedro
Publikováno v:
Oral Oncology. 40:409-417
Squamous cell carcinoma of the pharynx and larynx (SCCPL) is a genetically complex disease and is frequently associated with nonrandom chromosomal alterations. Fifty primary SCC of the pharynx (oropharynx, n=11, and hypopharynx, n=11) and larynx (n=2