Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ilir Ahmetgjekaj, Phd"'
Autor:
Ilir Ahmetgjekaj, PhD, Edlira Harizi, MD, Abdur Rahman, MD, Fjolla Hyseni, MD, Fareeha Nasir, MD, Arlind Decka, MD, Masum Rahman, MD, Kledisa Shemsi, MD, Kristi Saliaj, MD, Samar Akram, MD, Ina Kola, MD, Juna Musa, MD, MSc
Publikováno v:
Radiology Case Reports, Vol 17, Iss 4, Pp 1220-1224 (2022)
Cholesterol granulomas are chronic inflammatory lesions located primarily in the apex of the petrous part of the temporal bone. They are benign, tumor-like lesions, consisting of a cystic cavity filled with a chocolate-brown fluid and present as hype
Externí odkaz:
https://doaj.org/article/87224c0e6c424c1a8a6860cd52c28159
Autor:
Juna Musa, MD Msc, Masum Rahman, MD, Ali Guy, Clinical assistant professore, Erisa Kola, MD, Angela Guy, MD, Fjolla Hyseni, MD, Anisa Cobo, MD, Kristi Saliaj, MD, Fiona Bushati, MD, Ilir Ahmetgjekaj, Phd
Publikováno v:
Radiology Case Reports, Vol 16, Iss 6, Pp 1271-1275 (2021)
The artery of Percheron (AOP) represents a rare anatomic variant of the posterior circulation. It is a solitary trunk that provides bilateral arterial supply to the rostral midbrain and paramedian thalamus. AOP infarction presentation varies, most of
Externí odkaz:
https://doaj.org/article/455f79ffdf8044d8bbb1385fbf5fa040
Autor:
Juna Musa, MD Mcs, Masum Rahman, MD, Ali Guy, Clinical assistant professor, Angela Guy, PHD candidate, Kristi Saliaj, MD, Abu Bakar Siddik, MD, Fjolla Hyseni, MD, Ketjana Elezi, Pharmacist, Ina Kola, MD, Anisa Cobo, MD, Ilir Ahmetgjekaj, PhD.
Publikováno v:
Radiology Case Reports, Vol 16, Iss 6, Pp 1368-1373 (2021)
Moyamoya is a rare cerebrovascular disorder marked by chronic, gradual blockage of the circle of Willis arteries, leading to characteristic collateral vessels, specifically cerebral angiography. The disease can develop in children and adults, althoug
Externí odkaz:
https://doaj.org/article/f034cb10d9e2452185f0879cc23e4522
Autor:
Ilir Ahmetgjekaj, PhD, Masum Rahman, MD, Fjolla Hyseni, MD, Ali Guy, Kulsum Madani, MD, Kristi Saliaj, MD, Angela Guy, MD, PhD, Valon Vokshi, Ina Kola, MD, Juna Musa, MD, MSc
Publikováno v:
Radiology Case Reports, Vol 16, Iss 5, Pp 1075-1079 (2021)
Joubert Syndrome is a rare autosomal recessive genetic disorder characterized by a distinctive midbrain-hindbrain malformation that gives the appearance of “the molar tooth sign” on axial magnetic resonance imaging (MRI). Mutations in the implica
Externí odkaz:
https://doaj.org/article/43dd88c0499d44fbbae0a2f6c58d8a83