Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Charbel F. Matar"'
Autor:
Sara S. Jdiaa, Jad A. Degheili, Charbel F. Matar, Michele F. Mocadie, Chirine S. Khaled, Aline M. El Zakhem
Publikováno v:
African Journal of Urology, Vol 29, Iss 1, Pp 1-6 (2023)
Abstract Background Malakoplakia is a rare granulomatous inflammatory condition that can affect immunosuppressed patients. The genitourinary system is the most involved organ. We present a case of kidney failure caused by obstructing bladder lesions,
Externí odkaz:
https://doaj.org/article/d4eb4a7f032b479188f19dab7a005924
Autor:
Maria T. Bourlon, Brenda Jiménez Franco, Francisco J. Castro-Alonso, Christianne Bourlon, Charbel F. Matar, Emilie Gunn, Ophira Ginsburg, Gilberto Lopes, Eva Segelov
Publikováno v:
JCO Global Oncology, Vol , Iss 8 (2022)
PURPOSEGlobal Oncology is the movement to improve equitable access to cancer control and care, recognizing challenges because of economic and social factors between high-, middle-, and low-income countries (HIC, MIC, and LIC, respectively). The JCO G
Externí odkaz:
https://doaj.org/article/3eb7f25cc8ca40d6b77de6b94d10ce94
Autor:
Ali T. Taher, Achille Iolascon, Charbel F. Matar, Rayan Bou-Fakhredin, Lucia de Franceschi, Maria Domenica Cappellini, Wilma Barcellini, Roberta Russo, Immacolata Andolfo, Paul Tyan, Beatrice Gulbis, Yesim Aydinok, Nicholas P. Anagnou, Gabriela Amstad Bencaiova, Hannah Tamary, Patricia Aguilar Martinez, Gianluca Forni, Raffaele Vindigni, on behalf of the EHA Scientific Working Group on “Red Cells, Iron”
Publikováno v:
HemaSphere, Vol 4, Iss 4, p e446 (2020)
Abstract. Rare inherited anemias are a subset of anemias caused by a genetic defect along one of the several stages of erythropoiesis or in different cellular components that affect red blood cell integrity, and thus its lifespan. Due to their low pr
Externí odkaz:
https://doaj.org/article/ebe1f92cc10e4f88b146f066ed638641
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 12, p 4070 (2018)
With the continuing progress in managing patients with thalassemia, especially in the setting of iron overload and iron chelation, the life span of these patients is increasing, while concomitantly increasing incidences of many diseases that were les
Externí odkaz:
https://doaj.org/article/f4c727df1fa44cceb04b0d8771a5a336
Autor:
Imane El Dika, Jinru Shia, Carol L. Chen, Viktoriya Paroder, Alan Carver, Ali Shamseddine, Deborah Mukherji, Bhawna Sirohi, Precious Takondwa Makondi, Clara Asseily, Charbel F. Matar, Rawad Elias, Emily Slater, Marlon Steven Rosenbaum, Rekha Paramesawaran, William Breitbart, Ghassan K. Abou-Alfa
Publikováno v:
Journal of Gastrointestinal Oncology. 13:3321-3328
Publikováno v:
Holland‐Frei Cancer Medicine. :1-10
Autor:
Ronald LG Flumignan, Vinicius T Civile, Jéssica Dantas de Sá Tinôco, Patricia IF Pascoal, Libnah L Areias, Charbel F Matar, Britta Tendal, Virginia FM Trevisani, Álvaro N Atallah, Luis CU Nakano
Publikováno v:
Cochrane Database Syst Rev
Coronavirus disease 2019 (COVID-19) is a serious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The primary manifestation is respiratory insufficiency that can also be related to diffuse pulmonary microthrombosis in p
Autor:
Ibrahim G Tsolakian, Elie A. Akl, Maddalena Barba, Holger J. Schünemann, Lara A Kahale, Maram B Hakoum, Francesca Sperati, Victor E D Yosuico, Charbel F Matar, Irene Terrenato
Publikováno v:
Cochrane Database Syst Rev
BACKGROUND: Oral anticoagulants may improve the survival of people with cancer through an antithrombotic effect, yet increase the risk of bleeding. OBJECTIVES: To evaluate the efficacy and safety of oral anticoagulants in ambulatory people with cance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35b4be6f9e834ee1cd7c0a5abb7da962
https://europepmc.org/articles/PMC8498286/
https://europepmc.org/articles/PMC8498286/
Autor:
Elie A. Akl, Francesca Sperati, Lisa K. Hicks, Lara A Kahale, Maram B Hakoum, Holger J. Schünemann, Maddalena Barba, Victor E D Yosuico, Ibrahim Tsolakian, Charbel F Matar, Irene Terrenato
Publikováno v:
Cochrane Database Syst Rev
Background Multiple myeloma is a malignant plasma cell disorder characterised by clonal plasma cells that cause end-organ damage such as renal failure, lytic bone lesions, hypercalcaemia and/or anaemia. People with multiple myeloma are treated with i
Autor:
Ali T. Taher, Achille Iolascon, Roberta Russo, Charbel F Matar, Rayan Bou-Fakhredin, Immacolata Andolfo
Introduction: Fanconi anemia (FA) is a rare congenital disease that belongs to the family of congenital trilinear bone marrow failure. Most FA patients will suffer bone marrow failure and the main treatment relies on supportive measures or more recen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e6dea048f80f53637588e0f204dac9e
http://hdl.handle.net/11588/866916
http://hdl.handle.net/11588/866916