Zobrazeno 1 - 6
of 6
pro vyhledávání: '"A. Bourazza, MD"'
Publikováno v:
Radiology Case Reports, Vol 17, Iss 6, Pp 1870-1873 (2022)
Paget's disease of bone (PDB) is a progressive monostotic or polyostotic osteopathy with unknown cause. It is associated with the involvement of the nervous system. The cranial nerves, spinal roots, cauda equina, spinal cord, and brain can be affecte
Externí odkaz:
https://doaj.org/article/49c56425eb7e40429cfc49e418edf44a
Autor:
Aziz Ahizoune, MD, Moad Belouad, MD, Houda Alloussi, MD, Mohamed Allaoui, MD, Mohamed Hamid, MD, Ahmed Bourazza, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 5459-5464 (2024)
Breast cancer is the most frequently diagnosed cancer in women and is caused by the uncontrolled proliferation of breast cells. Metastases from breast cancer to the central nervous system have been described frequently in the literature, but dural me
Externí odkaz:
https://doaj.org/article/7201780cb0724c7cae6b7967113a1f3d
Publikováno v:
Radiology Case Reports, Vol 19, Iss 9, Pp 3724-3728 (2024)
Multiple system atrophy is a form of synucleinopathy with an unknown etiology that causes progressive neurodegeneration. It may affect the cerebellum, autonomic nerves, and pyramidal and extrapyramidal systems. We present the case of a 51-year-old ma
Externí odkaz:
https://doaj.org/article/5092daf384a647beb2a1198905048980
Publikováno v:
Radiology Case Reports, Vol 17, Iss 8, Pp 2616-2618 (2022)
Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon neurological disease defined as cerebral hemiatrophy with a contralateral motor deficit, facial asymmetry, and seizures. Classic imaging findings are cerebral hypoplasia, ventriculomegaly, paranasal
Externí odkaz:
https://doaj.org/article/c416d8febdae4b9593afeb047f9b5ebe
Publikováno v:
Radiology Case Reports, Vol 17, Iss 10, Pp 3863-3866 (2022)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary microangiopathy characterized by a genetic predisposition to small arteries of the brain. It is produced by a mutation in the NOTCH3
Externí odkaz:
https://doaj.org/article/b66749199e0445e49ad8da422beeb3cb
Publikováno v:
Radiology Case Reports, Vol 17, Iss 8, Pp 2798-2801 (2022)
Moyamoya disease is an unusual occlusive cerebrovascular condition commonly seen in children, marked by stenosis of the internal carotid artery and circle of Willis, causing, cerebral ischemia. Moyamoya syndrome is a Moyamoya-like arteriopathy with r
Externí odkaz:
https://doaj.org/article/8019adc9243c4ab69cc337ad96f54285