Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Angela Guy"'
Autor:
Juna Musa, Masum Rahman, Angela Guy, Ilir Ahmetgjekaj, Ali Guy, Ina Kola, Abu Bakar Siddik, Alireza Shoushtarizadaeh, Kristi Saliaj, Guri Hyseni, Fjolla Hyseni
Publikováno v:
Radiology Case Reports, Vol 16, Iss 10, Pp 3084-3089 (2021)
Trigeminal neuralgia is a pain condition that affects the face along the distribution of the trigeminal nerve and can be recurrent and chronic. Dandy-Walker syndrome is a complex congenital brain anomaly that occurs during embryonic development of th
Externí odkaz:
https://doaj.org/article/fada095a79b44943bd0a13f04561e177
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
Autor:
Ali Guy, Clinical Assistant Professor, Angela Guy, Phd, Masum Rahman, Marina Kokova, Azizjon Abdurakhimov, Azaliia Persits, Kristi Saliaj, Ina Kola, Anisa Cobo, Juna Musa, MD, MSc
Publikováno v:
Radiology Case Reports, Vol 16, Iss 4, Pp 789-794 (2021)
Sphenoid sinus fungal ball (FB) is a noninvasive fungal infection affecting predominantly immunocompetent middle-aged female patients. Common clinical manifestations include headaches, postnasal drip, and nasal discharge. In this case report, we pres
Externí odkaz:
https://doaj.org/article/562a0ed7a91b439c8734d3fb3689d139
Autor:
Fjolla Hyseni, Ali Guy, Fiona Bushati, Kristi Saliaj, Juna Musa, Masum Rahman, Anisa Cobo, Angela Guy, Erisa Kola, Ilir Ahmetgjekaj
Publikováno v:
Radiology Case Reports, Vol 16, Iss 6, Pp 1271-1275 (2021)
Radiology Case Reports
Radiology Case Reports
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
Autor:
Angela Guy, Kristi Saliaj, Marina Kokova, Anisa Cobo, Masum Rahman, Ali Guy, Azizjon Abdurakhimov, Azaliia Persits, Juna Musa, Ina Kola
Publikováno v:
Radiology Case Reports, Vol 16, Iss 4, Pp 789-794 (2021)
Radiology Case Reports
Radiology Case Reports
Sphenoid sinus fungal ball (FB) is a noninvasive fungal infection affecting predominantly immunocompetent middle-aged female patients. Common clinical manifestations include headaches, postnasal drip, and nasal discharge. In this case report, we pres
Autor:
Angela Guy, Ilir Ahmetgjekaj, Juna Musa, Fjolla Hyseni, Valon Vokshi, Ali Guy, Ina Kola, Kulsum Madani, Masum Rahman, Kristi Saliaj
Publikováno v:
Radiology Case Reports
Radiology Case Reports, Vol 16, Iss 5, Pp 1075-1079 (2021)
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 implicated
Autor:
Juna Musa, Inva Mamica, Kristi Saliaj, Henri Fero, Ali Guy, Ergys Cuka, Loran Rakovica, Viola Sulollari, Angela Guy
Publikováno v:
Acta Scientific Medical Sciences. 4:137-140
Autor:
Loran Rakovica, Vokshi, Fjolla Hyseni, Abu Bakar Siddik, Sherifi F, Eram Ahsan, Komoni F, Masum Rahman, Essa Mohamed, Juna Musa, Angela Guy, Samar Ikram
Publikováno v:
Archives of Clinical and Medical Case Reports.
Budd-Chiari syndrome (BCS) is a rare condition marked by a number of symptoms due to hepatic venous obstruction. A 40-year-old female patient presented with abdominal pain, distension, and dyspnea. An abdominal ultrasonogram showed hepatomegaly, sple