Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Juna Musa, MD MSc"'
Autor:
Fjolla Hyseni, MBBS, Diana Hla, BA, Abu Bakar Siddik, MBBS, Ilir Ahmetgjekaj, MBBS, Valon Vokshi, MBBS, Samar Ikram, MD, Abdur Rahman, MBBS, Alireza Shoushtarizadeh, MD, Kristi Saliaj, MBBS, Ali Guy, MD, Muhammad Tahir, MBBS, Ibrahim A. Bajwa, Essa A. Mohammed, PhD, Juna Musa, MD MSc
Publikováno v:
Radiology Case Reports, Vol 17, Iss 3, Pp 650-655 (2022)
Situs inversus totalis (SIT) is a rare developmental abnormality where the organs throughout both the thoracic cavity and abdomen are a mirror image of normal anatomy, often occurring concomitantly with other genetic and developmental defects. Acute
Externí odkaz:
https://doaj.org/article/720018b164ea49cd9903e34f5520a16c
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, MSc, Ahmad Parvinian, MD, Nathan Huber, PhD, Andrea Ferrero, PhD, Christopher Favazza, PhD, Anil Kurup, MD, Thomas Atwell, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 3517-3521 (2024)
Dual-energy or spectral computed tomography (CT) information may be obtained by either sending X-ray beams of different energy spectra through the patient or by discriminating the energy of the X-rays that reach the detector. The spectral signal is t
Externí odkaz:
https://doaj.org/article/f563713d37b94319b442782b5e4b10ea
Autor:
Fatos Sada, MD, PhD, Elton Cekaj, MD, Blerina, Saraci, MD, Ormira Shazi, MD, Abdallah Al-Madani, MD, Sepideh Jahanian, MD, Shamsun Nahar, MBBS, Juna Musa, MD, MSc, Keti Mamillo, MD, Dijon Musliu, MD, Murtaza Ahadi, MBBS, Florim Leniqi, BSc, Tamanna Agarwal, MD, Fjolla Hyseni, MD, PhD candidate, Valon Vokshi, MD, Adam Benjamin Fink, MD, FNU Deepali, MBBS, Jeton Shatri, MD, PhD, Sadi Bexheti, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 1, Pp 256-259 (2023)
Zinner syndrome is a rare congenital malformation of the mesonephric duct comprising of seminal vesicle cyst, ipsilateral renal agenesis, and ejaculatory duct obstruction. Clinical presentation varies with perineal pain, painful ejaculation, hematosp
Externí odkaz:
https://doaj.org/article/0481fd69175a4373aaee5aa439cf3c70
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, 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:
Fjolla Hyseni, MD, Edlira Harizi, MD, Rubén Blanco, MD, Robert Bido, MD, Jessie Pichardo, MD, Masum Rahman, MD, Muhammad Tahir, MD, Ali Guy, PhD, Sawsan Fathma, MD, Kledisa Shemsi, MD, Atiq ur Rehman Bhatti, MD, Fareeha Nasir, MD, Arlind Decka, MD, Samar Ikram, MD, Erisa Kola, MD, Juna Musa, MD, Msc
Publikováno v:
Radiology Case Reports, Vol 17, Iss 4, Pp 1251-1255 (2022)
Lumbar radiculopathy is a clinical condition defined by symptoms of pain, weakness, numbness, or tingling due to lumbar nerve root compression in levels L1-L4. Typically, it is characterized by a narrowing near the nerve root possibly caused by steno
Externí odkaz:
https://doaj.org/article/c7dbb6da3f0b4bc58dbec13ced16599b
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, Abu Bakar Siddik, MD, Ilir Ahmetgjekaj, MD, PhD, Masum Rahman, MD, Ali Guy, MD, Abdur Rahman, MD, Samar Ikram, MD, Erisa Kola, MD, Valon Vokshi, MD, Eram Ahsan, MD, Kristi Saliaj, MD, Fjolla Hyseni, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 16, Iss 9, Pp 2726-2730 (2021)
Langerhans Cell Histiocytosis (LCH) is a rare disorder sometimes called the disorder of the “monocyte-macrophage system”. This condition is characterized by the proliferation of abnormal Langerhans cells within different tissues. Skin rash is the
Externí odkaz:
https://doaj.org/article/cfac7c8797934cc6a6525d30d88975db