Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Georges Ibrahim"'
Publikováno v:
Case Reports in Vascular Medicine, Vol 2021 (2021)
Spontaneous resolution of cystic adventitial disease (CAD) is rare with occasional reports in the literature. In this case report, we are describing a 30-year-old man who presented with rapid onset of severe intermittent claudication and was diagnose
Externí odkaz:
https://doaj.org/article/f09aea2cffc24f6a9beac37d4dc7ec46
Publikováno v:
International Journal of Vascular Medicine, Vol 2021 (2021)
Retrograde popliteal access has long been established as an alternative to the antegrade approach to occlusive lesions in the superficial femoral artery (SFA). However, early reports with high complication rates (dissection, hematomas, aneurysms, and
Externí odkaz:
https://doaj.org/article/21248917e55c405ebd4673d3c5103575
Autor:
V. V. Mogila, Georges Ibrahim Nicolas
Publikováno v:
Ukrainian Neurosurgical Journal, Iss 2, Pp 50-53 (2005)
The pain syndrome is one of the principal components of clinical symptoms of such injuries. The complex regional pain syndrome is observed in high injuries of median nerve more frequently.Traumatic injuries of peripheral nerves are most frequent and
Externí odkaz:
https://doaj.org/article/967ed165f0de4f11906b466b92c291eb
Autor:
Georges Ibrahim Nicolas
Publikováno v:
Ukrainian Neurosurgical Journal, Iss 1, Pp 57-60 (2005)
Traumatic injury of median nerve consists from 20% to 35% of all injuries of nerves of upper extremities. This nerve is the main for arm and fingers flexors innervation. Symptoms of median nerve traumatic injury depend on it’s level, character and
Externí odkaz:
https://doaj.org/article/601609840d914f72a623fcdc9385d424
Autor:
Stephen M. Kaminsky, Laith Alyass, Ronald G. Crystal, Katie M. Stiles, Bishnu P. De, Christiana Salami, Clarisse Jose, Maria J. Chiuchiolo, Dolan Sondhi, Georges-Ibrahim Cisse, Katie Jackson
Publikováno v:
Human Gene Therapy. 31:819-827
Friedreich's ataxia (FA), an autosomal recessive disorder caused by a deficiency in the expression of frataxin (FXN), is characterized by progressive ataxia and hypertrophic cardiomyopathy. Although cardiac dysfunction is the most common cause of mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cec7bf43faa48e02af7f8323df4c4ba
https://doi.org/10.1089/hum.2019.363
https://doi.org/10.1089/hum.2019.363
Publikováno v:
International Journal of Vascular Medicine
International Journal of Vascular Medicine, Vol 2021 (2021)
International Journal of Vascular Medicine, Vol 2021 (2021)
Retrograde popliteal access has long been established as an alternative to the antegrade approach to occlusive lesions in the superficial femoral artery (SFA). However, early reports with high complication rates (dissection, hematomas, aneurysms, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abaca1ec399f9c41ab146bad1de3c5ba
http://europepmc.org/articles/PMC8149250
http://europepmc.org/articles/PMC8149250
Akademický článek
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Publikováno v:
Gene Reports. 4:33-36
Introduction Hepatitis C virus (HCV) is a common chronic infection worldwide affecting approximately 170 million people. 80% of acutely infected people fail to eliminate the virus and develop into the chronic phase. Some studies propose that activati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7532338c1ed799c76c3d5e47e54c6529
https://doi.org/10.1016/j.genrep.2016.02.007
https://doi.org/10.1016/j.genrep.2016.02.007
Publikováno v:
Southern Medical Journal. 103:823-827
Diagnosis of myelodysplastic syndrome/acute myeloid leukemia (MDS/AML) and chronic lymphocytic leukemia (CLL) in the same patient is extremely rare. We describe a 69-year-old CLL patient who developed MDS with ring sideroblasts 1 year after diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::058eda6e96430e0743f0a3d7f99d53c2
https://doi.org/10.1097/smj.0b013e3181e6d2b4
https://doi.org/10.1097/smj.0b013e3181e6d2b4
Autor:
Khalil M. Charafeddine, Georges Ibrahim, Samar Muwakkit, Ghazi Zaatari, Chantal Farra, Nada D. Najm, Rami Mahfouz
Publikováno v:
Cancer Genetics and Cytogenetics. 200:28-33
Translocations involving chromosomes 1 and 15 are uncommon in hematologic malignancies. So far, only 42 cases have been reported with t(1;15) as a reciprocal or complex chromosomal abnormalities. We herein report the first case in the literature, to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aaa7afd951016d1fb4437fddb2d5fb9
https://doi.org/10.1016/j.cancergencyto.2010.03.010
https://doi.org/10.1016/j.cancergencyto.2010.03.010