Zobrazeno 1 - 10
of 3 044
pro vyhledávání: '"neurofibromatosis type 2"'
Publikováno v:
Radiology Case Reports, Vol 19, Iss 9, Pp 3710-3714 (2024)
Schwannomatosis is a rare neurocutaneous syndrome characterized by the presence of multiple schwannomas along the peripheral nerves, distinctly excluding the vestibular nerves. It is recognized as the third principal form of neurofibromatosis, alongs
Externí odkaz:
https://doaj.org/article/e2a11a51710f4cf88c0e09c17847b83f
Publikováno v:
Oncology and Therapy, Vol 12, Iss 2, Pp 257-276 (2024)
Abstract Neurofibromatosis type 2 (NF2)-related schwannomatosis is a rare autosomal dominant monogenic disorder caused by mutations in the NF2 gene. The hallmarks of NF2-related schwannomatosis are bilateral vestibular schwannomas (VS). The current t
Externí odkaz:
https://doaj.org/article/736d80d3ef214f89ab11c788923a87b8
Publikováno v:
Neurologia Medico-Chirurgica, Vol 64, Iss 3, Pp 116-122 (2024)
Meningioma is the second most frequent tumor in patients with neurofibromatosis type 2 (NF2). The presence of meningioma is believed to be a negative prognostic marker in these patients. However, the molecular mechanisms involved in the tumorigenesis
Externí odkaz:
https://doaj.org/article/fb002a664324486eb4f1f5411e109506
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract NF2-related schwannomatosis (NF2-SWN) is a rare genetic disorder and is associated with progressive morbidities. This study aimed to investigate the relationship between NF2-SWN disease severity, health-related Quality of Life (QoL), and men
Externí odkaz:
https://doaj.org/article/67182173c8a34640926318ca0e2fd7b6
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-6 (2024)
Abstract Background Ependymomas are the third most common central nervous system tumor in the pediatric population; however, spinal ependymomas in children are rare. Ependymomas affecting the spinal cord most frequently occur in adults of 20–40 yea
Externí odkaz:
https://doaj.org/article/3966525dd0c94896b1ad58a8797248ec
Autor:
Vera Nickl, David Ziebolz, Charlotte Rumpel, Dennis Klein, Robert Nickl, Eva Rampeltshammer, Camelia M. Monoranu, Ralf-Ingo Ernestus, Cordula Matthies, Mario Löhr, Carsten Hagemann, Maria Breun
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
ObjectiveVestibular schwannomas (VS), benign tumors stemming from the eighth cranial nerve’s Schwann cells, are associated with Merlin gene mutations, inflammation, and the tumor microenvironment (TME), influencing tumor initiation, maintenance, an
Externí odkaz:
https://doaj.org/article/4d95d6ced64e4b15acd85a5f5093c924
Autor:
Takashi Yamauchi, Machi Suka
Publikováno v:
Environmental Health and Preventive Medicine, Vol 29, Pp 44-44 (2024)
Background: This study examined the association between neurological symptoms and quality of life (QoL) in patients with neurofibromatosis type 2 (NF2) using a national database of all patients who newly claimed for medical expense subsidies in Japan
Externí odkaz:
https://doaj.org/article/e614856152cb4d85b17614a1c3251978
Autor:
Yu Teranishi, Satoru Miyawaki, Masahiro Nakatochi, Atsushi Okano, Kenta Ohara, Hiroki Hongo, Daiichiro Ishigami, Yu Sakai, Daisuke Shimada, Shunsaku Takayanagi, Masako Ikemura, Daisuke Komura, Hiroto Katoh, Jun Mitsui, Shinichi Morishita, Tetsuo Ushiku, Shumpei Ishikawa, Hirofumi Nakatomi, Nobuhito Saito
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-13 (2023)
Abstract Although recent molecular analyses revealed that sporadic meningiomas have various genetic, epigenetic, and transcriptomic profiles, meningioma in patients with neurofibromatosis type 2 (NF2) have not been fully elucidated. This study invest
Externí odkaz:
https://doaj.org/article/36132233814845119abf3aa8a2f37537
Autor:
Zineb Izi, MD, Kaoutar Imrani, MD, Najwa Amsiguine, MD, Tlaite Oubaddi, MD, Nabil Moatassim Billah, PhD, Ittimade Nassar, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 8, Pp 2831-2835 (2023)
Neurofibromatosis type 2 (phacomatosis) is a rare inherited autosomal dominant condition defined by the development of numerous central neuronal tumors. In addition to classic intracranial schwannomas, intracranial and spinal meningiomas, and intrame
Externí odkaz:
https://doaj.org/article/981c163678e64cd3a7be3fade843ceb3
Publikováno v:
Cancers, Vol 16, Iss 8, p 1479 (2024)
(1) Background: NF2-related schwannomatosis, characterized by the development of bilateral vestibular schwannomas, often necessitates varied treatment approaches. Bevacizumab, though widely utilized, demonstrates variable effectiveness on hearing and
Externí odkaz:
https://doaj.org/article/28c64704bccd48c2a28271cfd928d997