Zobrazeno 1 - 10
of 1 984
pro vyhledávání: '"Intracranial haemorrhage"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Head trauma is a common reason for emergency department (ED) visits. Delayed intracranial hemorrhage (ICH) in patients with minor head trauma is a major concern, but controversies exist regarding the incidence of delayed ICH and discharge pl
Externí odkaz:
https://doaj.org/article/00248970816a471798c715aa5ab13ca1
Publikováno v:
The Journal of Haemophilia Practice, Vol 11, Iss 1, Pp 92-98 (2024)
Patients with acquired haemophilia A (PwAHA) can present with severe bleeding and may require lengthy treatment with bypassing agents and immunosuppression. We present two cases of the implementation of emicizumab in PwAHA. The first patient, an 82-y
Externí odkaz:
https://doaj.org/article/421bc4fc750a4b3db7ed635b111b9b85
Autor:
Lukas Goertz, Yosef Al-Sewaidi, Mahmoud Habib, David Zopfs, Benjamin Reichardt, Alexander Ranft, Christoph Kabbasch
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract The use of mobile head CT scanners in the neurointensive care unit (NICU) saves time for patients and NICU staff and can reduce transport-related mishaps, but the reduced image quality of previous mobile scanners has prevented their widespre
Externí odkaz:
https://doaj.org/article/d50046e4666540c3b8b127659a960d9f
Autor:
Joshua Y. P. Yeo, Kevin Soon Hwee Teo, En Ying Tan, Clyve Yaow, H. Hariz, H. S. Lim, B. J. M. Ng, Y. H. L. Wong, Cantiriga Subramaniam, Andrew Makmur, Weiping Han, Mark Y. Y. Chan, Ching-Hui Sia, Mingxue Jing, Benjamin Y. Q. Tan, David K. K. Tang, Leonard Leong Litt Yeo
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
Background and aimsEndovascular thrombectomy (EVT) is the current standard of care for large vessel occlusion (LVO) acute ischemic stroke (AIS); however, up to two-thirds of EVT patients have poor functional outcomes despite successful reperfusion. M
Externí odkaz:
https://doaj.org/article/16948ab889c04ab39977b08e3274b122
Autor:
Borboruah Luish, Dutta Anupam
Publikováno v:
The Journal of Haemophilia Practice, Vol 10, Iss 1, Pp 68-73 (2023)
Hereditary factor X (FX) deficiency is a rare autosomal recessive disorder that increases bleeding tendencies, ranging from epistaxis to intracranial haemorrhage (ICH), which can be life-threatening. Single factor concentrates are recommended for tre
Externí odkaz:
https://doaj.org/article/7272ec6bebcf4693a715acf70b96dee9
Publikováno v:
IET Computer Vision, Vol 17, Iss 2, Pp 170-188 (2023)
Abstract Intracranial haemorrhage (ICH) is a haemorrhagic disease that occurs in the ventricle or brain tissue and has a high probability of mortality and disability. For ICH, it is important to obtain a correct diagnosis in the early stages. Current
Externí odkaz:
https://doaj.org/article/b0499a7fa49b48ad8492037be382916f
Publikováno v:
Malaysian Family Physician, Vol 19, p 15 (2024)
Externí odkaz:
https://doaj.org/article/1e34c4fcde1a4d35b1456ccc35d31a96
Autor:
Sanchi Gagneja, Dileep Goyal, Hemlata Mittal, Savita Shekhawat, Devendra Sareen, Sukhanwar Sing Sandhu
Publikováno v:
Indian Journal of Neonatal Medicine and Research, Vol 11, Iss 4, Pp PO07-PO11 (2023)
Introduction: Hypernatremic dehydration is commonly found in the first week of neonatal life. Hypernatremia develops when water loss exceeds sodium loss, as in lactational failure with inadequate breastfeeding, or when sodium intake exceeds water int
Externí odkaz:
https://doaj.org/article/fa2f32e6126843ab8a7065b5173e1d7f
Autor:
Noha Negm, Ghadah Aldehim, Faisal Mohammed Nafie, Radwa Marzouk, Mohammed Assiri, Mohamed Ibrahim Alsaid, Suhanda Drar, Sitelbanat Abdelbagi
Publikováno v:
IEEE Access, Vol 11, Pp 75474-75483 (2023)
Intracranial haemorrhage (ICH) has become a critical healthcare emergency that needs accurate assessment and earlier diagnosis. Due to the high rates of mortality (about 40%), the early classification and detection of diseases through computed tomogr
Externí odkaz:
https://doaj.org/article/6853e26b8e42453d9b4ea73d52a6226d
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-5 (2023)
Abstract Background Primary familial brain calcification (PFBC), habitually called Fahr’s disease, is characterized by bilateral calcification of the basal ganglia, accompanied by extensive calcification of the cerebellar dentate nucleus, brainstem
Externí odkaz:
https://doaj.org/article/b7d3d97ed97a4fae9fcea7c7ff03c662