Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Behyamet Onka"'
Autor:
Thierry Romeo Yehouenou Tessi, MD, Behyamet Onka, MD, Maniani Abdel ilah Drissi, MD, Hounayda Jerguigue, MD, Rachida Latib, Prof., Youssef Omor, Prof.
Publikováno v:
Radiology Case Reports, Vol 16, Iss 9, Pp 2537-2541 (2021)
Cholangiocarcinoma is a rare liver tumor with three types: intrahepatic, extrahepatic, and perihilar, which alone account for about 50% of cases. The diagnosis is late with a poor prognosis. Imaging through Bili MRI and CT scan plays an essential rol
Externí odkaz:
https://doaj.org/article/dad3fa4fbaa448a0917d945db0aff597
Autor:
Behyamet Onka, Resident doctor, Selma Khouchoua, Resident doctor, Tessi Romeo Thierry Yehouenou, Resident doctor, Hounayda Jerguigue, Spécialist doctor, Rachida Latib, Professor, Youssef Omor, Professor
Publikováno v:
Radiology Case Reports, Vol 16, Iss 8, Pp 2025-2030 (2021)
The Nutcracker Syndrome is a rare and often unrecognized cause of chronic pelvic pain and left back pain. These symptoms are due to the left renal vein compression between the aorta and the superior mesenteric artery (anterior nutcracker) or between
Externí odkaz:
https://doaj.org/article/e74a34c889d243a7953fb69daa69b9e0
Autor:
Ibrahima Dokal Diallo, Najlae Lrhorfi, Wend-Yam Mohamed Traoré, Behyamet Onka, Latifa Chat, Nazik Allali
Publikováno v:
Global Pediatric Health, Vol 9 (2022)
Cerebral aspergillosis is a fungal infection with a bad prognosis. It usually occurs in immunocompromised patients and manifests itself .Cross-sectional imaging reveals suggestive lesions.
Externí odkaz:
https://doaj.org/article/0b4d3e12faf44d53bda5d96793f884ad
Autor:
Ibrahima Dokal Diallo, Zaynab Iraqi Houssaini, Mehdi Tantaoui, Wend-Yam Mohamed Traoré, Behyamet Onka, Siham El Haddad, Latifa Chat, Nazik Allali
Publikováno v:
Global Pediatric Health, Vol 9 (2022)
Von Recklinghausen disease is the most common phacomatosis. It can affect many systems, including the bone system. Through these 2 cases, we illustrate the bone manifestations of this disease.
Externí odkaz:
https://doaj.org/article/8e3795128d02488b96ad402eae10071f
Autor:
Romeo Thierry Yehouenou Tessi, Behyamet Onka, Asaad El Bakkari, Hounayda Jerguigue, Rachida Latib, Youssef Omor
Publikováno v:
SAGE Open Medical Case Reports, Vol 10 (2022)
Pneumocystis jiroveci pneumonia is a common pathology in HIV-infected but also in uninfected immunocompromised individuals. The pandemic coronavirus disease 2019 (COVID-2019) is a new type of coronavirus disease caused by SARS-COV-2, and the chest im
Externí odkaz:
https://doaj.org/article/a92b70f69bb74313b491011cc5fcd946
Autor:
Daoud Ali Mohamed MhD, Amarkak Waiss MhD, Behyamet Onka MhD, Walid Mohamed MhD, Nazik Allali PhD, Latifa Chat PhD, Siham El Haddad PhD
Publikováno v:
Global Pediatric Health, Vol 8 (2021)
Pulmonary Arteriovenous Malformations (PAVMs) are structurally abnormal vascular communications between pulmonary arteries and pulmonary veins, which bypass the normal capillary bed and cause a low resistance right-to-left shunt with refractory hypox
Externí odkaz:
https://doaj.org/article/6f7d3ee3d65745c7b9c294ac5a806bd5
Publikováno v:
International Journal of Case Reports and Images. 13:153-155
No Abstract
Autor:
Rachida Latib, Maniani Abdel ilah Drissi, Thierry Romeo Yehouenou Tessi, Behyamet Onka, Youssef Omor, Hounayda Jerguigue
Publikováno v:
Radiology Case Reports, Vol 16, Iss 9, Pp 2537-2541 (2021)
Radiology Case Reports
Radiology Case Reports
Cholangiocarcinoma is a rare liver tumor with three types: intrahepatic, extrahepatic, and perihilar, which alone account for about 50% of cases. The diagnosis is late with a poor prognosis. Imaging through Bili MRI and CT scan plays an essential rol
Autor:
Firdaous Touarsa, Daoud Ali Mohamed, Behyamet Onka, Soufiane Rostoum, Najwa Ech-Cherif El Kettani, Meriem Fikri, Mohamed Jiddane
Publikováno v:
BJR|case reports. 8
Aceruloplasminemia is a rare autosomal recessive disorder of iron accumulation in the brain. It is one of the subtypes of Neurodegeneration with brain iron accumulation and is characterized by the uniform involvement of all basal ganglia, thalami, de
Autor:
Behyamet Onka, Daoud ali Mohamed, Romeo Thierry Tessi Yehouenou, Boris Adeyemi, Wend-Yam Mohammed Traore, Mbina Mbougou Kevin arthur, Hounayda Jerguigue, Rachida Latib, Youssef Omor
Publikováno v:
BJR|case reports. 8
lynch syndrome (LS) is an autosomal dominant genetic disorder with incomplete penetration caused by a germline mutation in one of the genes of the deoxyribonucleic acid (DNA) mismatch repair system (MMR) namely: mutL homolog 1 (MLH1), mutS homolog 2