Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Dimitri, Maamari"'
Autor:
Raya Saab, Nathalie K. Zgheib, Samar Muwakkit, Habib El-Khoury, Maya Basbous, Dimitri Maamari
Publikováno v:
Personalized Medicine. 18:431-439
Aim: To evaluate the association between candidate genetic polymorphisms and glucocorticoid-induced osteonecrosis in Arab children treated for acute lymphoblastic leukemia. Methods: A total of 189 children treated for acute lymphoblastic leukemia wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf3bb45170931621e9633155367f2a5b
https://doi.org/10.2217/pme-2020-0167
https://doi.org/10.2217/pme-2020-0167
Publikováno v:
Circulation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b3ba32cd9c8ce5f3193744dc0959bb6
https://doi.org/10.1161/circulationaha.121.057028
https://doi.org/10.1161/circulationaha.121.057028
Publikováno v:
Pharmacogenomics and Personalized Medicine. 13:295-317
Despite major advances in the management and high cure rates of childhood acute lymphoblastic leukemia (ALL), patients still suffer from many drug-induced toxicities, sometimes necessitating dose reduction, or halting of cytotoxic drugs with a second
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd354466faea44b4908cd291c08c8262
https://doi.org/10.2147/pgpm.s239602
https://doi.org/10.2147/pgpm.s239602
Autor:
Ahmad Sweid, Kavya Shivashankar, Michael P Baldassari, Dimitri Maamari, Carol L. Shields, Li-Anne S Lim, Pavlos Texakalidis, Stavropoula Tjoumakaris, Somnath Das, David Ancona-Lezama, Lauren A Dalvin, Batoul Hammoud, Vivian Xu, Pascal Jabbour
Publikováno v:
Neurosurgery. 87:956-963
Background The introduction of intra-arterial chemotherapy (IAC) for treatment of retinoblastoma considerably changed the paradigm by which this disease is managed, with event-free survival rates being above 70%. Objective To analyze efficacy of IAC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::901bf325b3cd907cae0cdd1169fdc14a
https://doi.org/10.1093/neuros/nyaa142
https://doi.org/10.1093/neuros/nyaa142
Autor:
Krishna G Aragam, Kiran Biddinger, Sean J Jurgens, Minxian Wang, James Pirruccello, Dimitri Maamari, Mark Chaffin, Seung H Choi, Valerie Morrill, Christopher Newton-cheh, Amit V Khera, Steven A Lubitz, Patrick T Ellinor
Publikováno v:
Circulation. 144
Introduction: Genetic testing for non-ischemic dilated cardiomyopathy (DCM) currently comprises assessment of rare (monogenic) mutations in DCM-relevant genes. The role of a common-variant (polygenic) predictor for DCM has yet to be evaluated. Method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b000eaa69300d4c7ab50a33b18c4848c
https://doi.org/10.1161/circ.144.suppl_1.13271
https://doi.org/10.1161/circ.144.suppl_1.13271
Autor:
Nathalie K, Zgheib, Habib, El-Khoury, Dimitri, Maamari, Maya, Basbous, Raya, Saab, Samar A, Muwakkit
Publikováno v:
Personalized medicine. 18(5)
Lay abstract This study aimed at uncovering variants in the genetic material of Arab children, that might predispose them to develop a specific treatment-related adverse effect, during their therapy for acute lymphoblastic leukemia (a type of blood c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::93bbfb22a19cf0dc1e2e87d2c2c09a73
https://pubmed.ncbi.nlm.nih.gov/34406079
https://pubmed.ncbi.nlm.nih.gov/34406079
Autor:
Stavropoula Tjoumakaris, Nabeel Herial, Maureen DePrince, Victor Romo, Michael R. Gooch, Dimitri Maamari, Hekmat Zarzour, Ahmad Sweid, David Hasan, Joshua H. Weinberg, Pascal Jabbour, Tyler D Alexander, Sunidhi Ramesh, Daniella Wong, Robert H. Rosenwasser, Batoul Hammoud, Jaime A. Dougherty
Publikováno v:
Stroke and Vascular Neurology
Stroke and Vascular Neurology, Vol 5, Iss 1 (2020)
Stroke and Vascular Neurology, Vol 5, Iss 1 (2020)
Care for acute ischaemic stroke is one of the most rapidly evolving fields due to the robust outcomes achieved by mechanical thrombectomy. Large vessel occlusion (LVO) accounts for up to 38% of acute ischaemic stroke and comes with devastating outcom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4837fa3ab4b71e9fff015933fa2f4470
http://europepmc.org/articles/PMC7213503
http://europepmc.org/articles/PMC7213503
Autor:
Kiran J, Biddinger, Sean J, Jurgens, Dimitri, Maamari, Liam, Gaziano, Seung Hoan, Choi, Valerie N, Morrill, Jennifer L, Halford, Amit V, Khera, Steven A, Lubitz, Patrick T, Ellinor, Krishna G, Aragam
Publikováno v:
JAMA cardiology, 7(7), 715-722. American Medical Association
JAMA Cardiol
JAMA Cardiol
IMPORTANCE: Hypertrophic cardiomyopathy (HCM) is a leading cause of sudden cardiac death in young people. Although rare genetic variants are well-established contributors to HCM risk, common genetic variants have recently been implicated in disease p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::491ee30da3ee13f58be82075a66751ad
https://doi.org/10.1001/jamacardio.2022.1061
https://doi.org/10.1001/jamacardio.2022.1061