Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ina Kola, MD"'
Autor:
Edlira Harizi, MD, Kledisa Shemsi, MD, Erisa Kola, MD, Fjolla Hyseni, MD, Ina Kola, MD, Mohammad Abubaker Siddique, MD, Jafor Sadeque, MD, Arlind Decka, MD, Migena Dervishi, MD, Fareeha Nasir, MD, Livia Capi, MD, Ivan Ayala, MD, Ammy Shankar Ghosh, MD, Sanzida Sharmin Swarna, MD, Juna Musa, MD, MBBS, Ilir Ahmetgjekaj, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 10, Pp 3669-3673 (2022)
Acute transverse myelitis is an inflammatory condition covering the entire cross section of the spinal cord, spreading on two or more vertebral segments, without evidence of a compressive lesion. This shows clinically as an acute or subacute onset of
Externí odkaz:
https://doaj.org/article/7f860207c03348fbb2b9424377787237
Autor:
Serbeze Kabashi, MD, Ilir Ahmetgjekaj, Edlira Harizi, MD, Fjolla Hyseni, MD, Erisa Kola, MD, Valon Vokshi, MD, Guri Hyseni, MD, Ina Kola, MD, Humza Haroon, MD, Masum Rahman, MD, Kledisa Shemsi, MD, Arlind Decka, MD, Livia Capi, MD, Kaltrina Goçaj, MD, Juna Musa, MD, MSc
Publikováno v:
Radiology Case Reports, Vol 17, Iss 9, Pp 2940-2945 (2022)
Tumors of the pineal region are a rare clinical entity, comprising approximately 3%-8% of pediatric tumors. Based on their histopathological features, they are typically classified as pineal parenchymal tumors and germ cell tumors, with the latter be
Externí odkaz:
https://doaj.org/article/82933cd6dfdf4becbafac6de66be9115
Autor:
Ermira Aliu, MD, Juna Musa, MD, MSc, Anusha Parisapogu, MBBS, Erisa Kola, MD, Fjolla Hyseni, MD, Ina Kola, MD, Alejandro Obando Blandón, MD, Pooja Roy, MD, Kampa Prathima, MD, Chandalji Naik Banavath, MD, Pooja Kumbha, MD, Shaik Mashood Tappa, MD, Jasmine Saini, MD, Srikrishnan Pichuthirumalai, MD, Ilir Ahmetgjekaj, Assoc. Prof. Dr
Publikováno v:
Radiology Case Reports, Vol 17, Iss 9, Pp 3147-3150 (2022)
Septo-optic dysplasia (SOD) is a rare congenital disorder occurring in only 1 in 10,000 live births. Initially it was described in 1941 by Reeves and further discussed by the French-Swiss neurologist de Morsier (1956) as the disease further addressed
Externí odkaz:
https://doaj.org/article/34de81773f8944099054a965f966f2cb
Autor:
Ilir Ahmetgjekaj, MD, Erisa Kola, MD, Anusha Parisapogu, MD, Fjolla Hyseni, MD, PhD, Pooja Roy, MD, Anid Hassan, MBBS, Ina Kola, MD, Hafsa Safeer Mian, MBBS, Pooja Kumbha, MD, Supti Dev Nath, MBBS, Tias Saha, MD, Zaina Syed, BS, Saiyara Sheikh Shama, MBBS, Jaclyn Tan Wohlers, MD, Juna Musa, MD, MCS
Publikováno v:
Radiology Case Reports, Vol 17, Iss 9, Pp 3243-3246 (2022)
Gorham-Stout disease (GSD) also known as vanishing bone disease is an idiopathic and rare condition characterized by gross and progressive bone loss along with excessive growth of vascular and lymphatic tissue. Very little is known about the pathogen
Externí odkaz:
https://doaj.org/article/068c45d851924eec8015977000aa8a33
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:
Erisa Kola, MD, Arben Gjata, Professor, Ina Kola, MD, Ali Guy, Assistant prof, Juna Musa, MD, Msc, Valbona Biba, MD, Vladimir Filaj, MD, Edlira Horjeti, MD, Daniela Nakuci, MD, Anisa Cobo, MD, Kristi Saliaj, MD, Mehdi Alimehmeti, Professor
Publikováno v:
Radiology Case Reports, Vol 16, Iss 11, Pp 3191-3195 (2021)
Ectopic thyroid tissue is a rare developmental abnormality arising from an aberration in the normal migration of the thyroid gland, from the floor of the primitive foregut to its final position. It is usually asymptomatic, often being diagnosed as an
Externí odkaz:
https://doaj.org/article/7c0e5c7e2a714374bd65bbc16266d9cc
Autor:
Juna Musa, MD, Msc, Masum Rahman, MD, Kristi Saliaj, MD, Abu Bakar Siddik, MD, Ronny Khadra, Ali Guy, clinical assisrant professor, Qemajl Aliu, MD, Kulsum Madani, MD, Ina Kola, MD, Elton Ceka, MD
Publikováno v:
Radiology Case Reports, Vol 16, Iss 6, Pp 1410-1419 (2021)
Primitive vein popliteal aneurysms are rare and potentially fatal vascular disorders. The most dangerous complications of popliteal vein aneurysms are thromboembolic events, mainly pulmonary embolisms, a life-threatening event that requires a timely
Externí odkaz:
https://doaj.org/article/2ddf96c09e3544c987295208978f13fb
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