Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Amjad Samara"'
Publikováno v:
Radiology Case Reports, Vol 15, Iss 7, Pp 863-866 (2020)
Peters’ anomaly is a rare congenital eye condition characterized by anterior segment dysgenesis and commonly presents as unilateral or bilateral corneal opacity in the early neonatal period. Peters’ anomaly is often associated with congenital bra
Externí odkaz:
https://doaj.org/article/abc28ad07fa2446190fa4f33cdc37539
Autor:
Amjad Samara, Rachel Rahn, Olga Neyman, Ki Yun Park, Ahmad Samara, Bess Marshall, Joseph Dougherty, Tamara Hershey
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-14 (2019)
Abstract Wolfram syndrome is a rare multisystem disorder caused by mutations in WFS1 or CISD2 genes leading to brain structural abnormalities and neurological symptoms. These abnormalities appear in early stages of the disease. The pathogenesis of Wo
Externí odkaz:
https://doaj.org/article/d1a0ded280414884a78b89ab597cc6ed
Autor:
Amjad Samara, MD, Jordan Nepute, MD, Hsiang-Chih Lu, MD, PhD, Richard J. Perrin, MD, PhD, Rami W. Eldaya, MD, MBA
Publikováno v:
Radiology Case Reports, Vol 14, Iss 12, Pp 1478-1482 (2019)
Langerhans Cell Histiocytosis (LCH) is a rare disorder characterized by neoplastic proliferation of Langerhans-type dendritic cells. LCH is most frequently encountered in the pediatric populations, and involvement of the skeletal system is a common m
Externí odkaz:
https://doaj.org/article/a3b0b15372194271acba536887644187
Autor:
Cullen Soares, Amjad Samara, Matthew F. Yuyun, Justin B. Echouffo‐Tcheugui, Ahmad Masri, Ahmad Samara, Alan R. Morrison, Nina Lin, Wen‐Chih Wu, Sebhat Erqou
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 19 (2021)
Background Studies have reported that people living with HIV have higher burden of subclinical cardiovascular disease, but the data are not adequately synthesized. We performed meta‐analyses of studies of coronary artery calcium and coronary plaque
Externí odkaz:
https://doaj.org/article/671194474cb14d9f9a32841cc1dc8420
Autor:
Dhruv Mahtta, Ahmed Altibi, Mohamed M. Gad, Amjad Samara, Amr F. Barakat, Rodrigo Bagur, Hend Mansoor, Hani Jneid, Salim S. Virani, Mamas A. Mamas, Ahmad Masri, Islam Y. Elgendy
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 18 (2021)
Background Well‐conducted meta‐analyses are considered to be at the top of the evidence‐based hierarchy pyramid, with an expansion of these publications within the cardiovascular research arena. There are limited data evaluating the trends and
Externí odkaz:
https://doaj.org/article/daf0ceb58bea4b3ebb17d717c7a326d2
Posterior reversible encephalopathy syndrome with isolated infratentorial involvement: A case report
Publikováno v:
Radiology Case Reports, Vol 14, Iss 5, Pp 576-580 (2019)
Posterior reversible encephalopathy syndrome (PRES) is a clinical and radiological entity of acute neurological symptoms associated with characteristic MRI finding. Vasogenic edema in the white matter of parieto-occipital regions is the classical MRI
Externí odkaz:
https://doaj.org/article/81c964c125b64e6aa34cbaa085c6d715
Autor:
Amjad Samara, Tatianna Murphy, Jeremy Strain, Jerrel Rutlin, Peng Sun, Olga Neyman, Nitya Sreevalsan, Joshua S. Shimony, Beau M. Ances, Sheng-Kwei Song, Tamara Hershey, Sarah A. Eisenstein
Publikováno v:
Frontiers in Human Neuroscience, Vol 13 (2020)
Human obesity is associated with low-grade chronic systemic inflammation, alterations in brain structure and function, and cognitive impairment. Rodent models of obesity show that high-calorie diets cause brain inflammation (neuroinflammation) in mul
Externí odkaz:
https://doaj.org/article/af9489b989a94c56b361b757fe9fa3ef
Publikováno v:
American Journal of Ophthalmology. 243:10-18
To report long-term ophthalmic findings in Wolfram syndrome, including rates of visual decline, macular thinning, retinal nerve fiber layer (RNFL) thinning, and outer plexiform layer (OPL) lamination.Single-center, cohort study.A total of 38 particip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67a543ab789389a17da59de87dead2a0
https://doi.org/10.1016/j.ajo.2022.07.003
https://doi.org/10.1016/j.ajo.2022.07.003
Publikováno v:
Current Problems in Diagnostic Radiology. 51:747-758
Phakomatoses, or neurocutaneous syndromes, are a heterogeneous group of rare genetic disorders that predominantly affect structures arising from the embryonic ectoderm, namely the skin, eye globe, retina, tooth enamel, and central nervous system. Oth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b796bc5e07d44c4aed9afef58f753e8
https://doi.org/10.1067/j.cpradiol.2021.07.002
https://doi.org/10.1067/j.cpradiol.2021.07.002
Publikováno v:
Multiple Sclerosis and Related Disorders. :104768
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e69d9e252aba310a2a6a2f57ac901be
https://doi.org/10.1016/j.msard.2023.104768
https://doi.org/10.1016/j.msard.2023.104768