Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Jessica Marquard"'
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-6 (2023)
Abstract Background The new presentation of pheochromocytoma or paraganglioma in pregnancy is very rare and can be life-threatening for mother and child. Case presentation We present the case of a 26-year-old gravida 3 para 2 otherwise healthy Caucas
Externí odkaz:
https://doaj.org/article/6fd87081aacd485395c8a1c56334f2e4
Autor:
Shraddha Narechania, Amrita Bath, Laleh Ghassemi, Chetan Lokhande, Abdo Haddad, Ali Mir Yousuf, Jessica Marquard, K. V. Gopalakrishna
Publikováno v:
Case Reports in Endocrinology, Vol 2015 (2015)
A young healthy postpartum mother presented with intermittent high fevers and tachycardia. Appropriate testing was done to rule out infectious causes including pan cultures but no identifiable infectious source was found. A CT of the abdomen showed a
Externí odkaz:
https://doaj.org/article/ee33558e8ea34ba5bac557fd8ececbcd
Autor:
Katherine M. Miller, Firas Sbeih, Kevin Contrera, Chandana A. Reddy, Jessica Marquard, Charis Eng, Robert R. Lorenz
Publikováno v:
Otolaryngology–Head and Neck Surgery.
Autor:
Jessica Marquard, Meng Yao, Mariam AlHilli, Roberto Vargas, Caitlin Carr, Jessica Son, Chad M. Michener, A. Priyadarshini
Publikováno v:
Gynecologic Oncology. 159:712-720
To evaluate clinicopathologic characteristics and survival impact associated with mismatch repair (MMR) deficient subgroups of endometrial cancer (EC) in patients undergoing universal screening for Lynch Syndrome.A retrospective cohort study using a
Endometrial cancer in young women: prognostic factors and treatment outcomes in women aged ≤40 years
Autor:
Caitlin Carr, Chad M. Michener, Ji Son, Meng Yao, A. Priyadarshini, Milena Radeva, Mariam AlHilli, Jessica Marquard
Publikováno v:
International Journal of Gynecologic Cancer. 30:631-639
ObjectiveEndometrial cancer in pre-menopausal patients aged ≤40 years is rare and poses both diagnostic and management challenges. The goal of this study was to investigate the clinical and pathologic factors associated with endometrial cancer in t
Autor:
Brandon Bungo, Hetty E. Carraway, Manmeet Ahluwalia, Petros Grivas, Jessica Marquard, Davendra Sohal, Zade Akras, Pauline Funchain, Brandie Leach
Publikováno v:
JCO precision oncology. 3
PURPOSE It has been estimated that 5% to 10% of cancers are due to hereditary causes. Recent data sets indicate that the incidence of hereditary cancer may be as high as 17.5% in patients with cancer, and a notable subset is missed if screening is so
Autor:
Karen Hurley, Brandie Heald, David Liska, Matthew F. Kalady, Emma Keel, James M. Church, Jessica Marquard, Charis Eng, Gautam Mankaney, Carol A. Burke
Publikováno v:
Journal of medical genetics. 58(12)
BackgroundHereditary colorectal cancer (HCRC) syndromes account for 10% of colorectal cancers but remain underdiagnosed. This feasibility project tested the utility of an artificial intelligence-based chatbot deployed to patients scheduled for colono
Autor:
Lisa LaGuardia, Loretta Arroyo, Matthew F. Kalady, Crowe D, Xhileta Xhaja, Brandie Leach, James M. Church, Hennie Hasson, DaSilva G, Margaret O'Malley, Carol A. Burke, B Jiminez, Jessica Marquard, Karen Hurley
Publikováno v:
Revista Médica Clínica Las Condes, Vol 28, Iss 4, Pp 561-568 (2017)
INTRODUCCION El Registro de Cancer Colorrectal Hereditario es uno de los registros mas antiguos y mas grandes de su tipo. Incluye a los pacientes con todos los sindromes hereditarios de cancer colorrectal, utilizando los tres enfoques basicos, la ate
Programmable Logic Controllers are an integral component for managing many different industrial processes (e.g., smart building management, power generation, water and wastewater management, and traffic control systems), and manufacturing and control
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6843567a50bf984d6b47fbfe2842873e
http://arxiv.org/abs/1911.06304
http://arxiv.org/abs/1911.06304
Publikováno v:
Seminars in Oncology. 43:609-614
Hereditary cancer syndromes generally account for 5%-10% of malignancies. While these syndromes are rare, affected patients carry significantly elevated risks of developing cancer, as do their at-risk relatives. Identification of these patients is cr