Zobrazeno 1 - 10
of 1 851
pro vyhledávání: '"G Popescu"'
Publikováno v:
Romanian Neurosurgery, Vol 38, Iss Special Issue (2024)
Introduction Cerebral and spinal cord cavernomas are vascular anomalies of the nervous system characterized by dilated vessels lined with a single layer of endothelium. They exhibit minimal blood flow and can occur in both the brain and spinal cor
Externí odkaz:
https://doaj.org/article/c903c28fb0e445c68f60d6f4d3c9b837
Publikováno v:
Romanian Neurosurgery, Vol 38, Iss Special Issue (2024)
Introduction Crouzon syndrome is a genetic disorder caused by mutations in the FGFR2 gene, leading to premature fusion of cranial sutures (craniosynostosis) and resulting in distinct craniofacial abnormalities such as a beaked nose, shallow orbits
Externí odkaz:
https://doaj.org/article/5d93b646797640d0aa570f19770e0f04
Autor:
D. Peptenatu, A. M. Băloi, O. Andronic, A. Bolocan, N. Cioran, A. K. Gruia, A. Grecu, T. C. Panciu, L. Georgescu, I. Munteanu, A. Pistol, F. Furtunescu, I. R. Strâmbu, E. Ibrahim, D. Băiceanu, G. G. Popescu, D. Păduraru, V. Jinga, B. Mahler
Publikováno v:
GeoHealth, Vol 8, Iss 2, Pp n/a-n/a (2024)
Abstract The study proposes a dynamic spatio‐temporal profile of the distribution of tuberculosis incidence and air pollution in Romania, where this infectious disease induces more than 8,000 new cases annually. The descriptive analysis for the yea
Externí odkaz:
https://doaj.org/article/a182436ad9314fbcb528dfdce457886e
Publikováno v:
Scientific Papers Animal Science and Biotechnologies, Vol 41, Iss 1, Pp 671-671 (2023)
Communication lives in the very heart of an organization. Any effort of development in an organization should take into consideration primarily human resources and their way of achieving goals through efficient communication. The main features of org
Externí odkaz:
https://doaj.org/article/a3b63cbcdec74ee89a606881bfabcbea
Publikováno v:
Romanian Neurosurgery, Vol 36, Iss 4 (2023)
Background: Neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2) are rare tumoral suppressor syndromes, triggered by an abnormal mutation in a tumour suppressor gene (TSG) (1). Each of these syndromes represents an orphan disease (by its
Externí odkaz:
https://doaj.org/article/54ec5841d1064dc2b8e0acd6545b15a4
Publikováno v:
Transactions on Cryptographic Hardware and Embedded Systems, Vol 2022, Iss 4 (2022)
Security evaluations for full cryptographic keys is a very important research topic since the past decade. An efficient rank estimation algorithm was proposed at FSE 2015 to approximate the empirical guessing entropy remaining after a side-channel at
Externí odkaz:
https://doaj.org/article/6796b366cea84e2e96c4b63d503cace6
Publikováno v:
Proceedings of the International Multidisciplinary Scientific GeoConference SGEM. 2022, Vol. 22, p447-454. 8p.
Autor:
F. Stoica, G. Popescu, Francesca Paslaru, Anamaria Gheorghiu, A.C. Paslaru, M. Apostol, M.C. Zaharia, R. M. Gorgan
Publikováno v:
Romanian Neurosurgery, Vol 36, Iss 2 (2022)
Glomus jugulare tumours are extremely rare, slow-growing, hypervascular tumours that arise within the jugular foramen of the temporal bone and frequently involve the lower cranial nerves. We performed a retrospective study for patients treated betwee
Externí odkaz:
https://doaj.org/article/a8034347ad55436f82829c6366db0db8
Autor:
G. Popescu, Francesca Paslaru, Anamaria Gheorghiu, A.C. Paslaru, M. Apostol, M.C. Zaharia, M. Popescu, R.M. Gorgan
Publikováno v:
Romanian Neurosurgery, Vol 36, Iss 2 (2022)
Hemangioblastoma is a rare, benign, highly vascularized tumour, that usually presents a muriform nodule. The most frequent localization is the posterior cranial fossa. The frequency of this spinal lesion is very low, representing less than 5% of spin
Externí odkaz:
https://doaj.org/article/1bbae84c5ddf4774b9aae36ac9e1678c
Autor:
G. Popescu, Francesca Paslaru, A. C. Paslaru, M. Apostol, M.C. Zaharia, M. Popescu, R. M. Gorgan
Publikováno v:
Romanian Neurosurgery, Vol 36, Iss 2 (2022)
Background: Diffuse gliomas are the most frequent primary central nervous system (CNS) neoplasms, originating from the parenchyma itself, oligodendrogliomas accounting for approximately 10% of cerebral gliomas. For the past 20 years, the study of gen
Externí odkaz:
https://doaj.org/article/df2b4e3e9bff483b9ce676c6a1fdd606