Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Isabel Gugel"'
Publikováno v:
Children, Vol 9, Iss 4, p 490 (2022)
Vestibular schwannomas (VS) usually manifest between the 5th and 8th decade of life. Most pediatric cases are associated with Neurofibromatosis type 2 and sporadic VS are rare in this age group. Few case series have been published. We report on our i
Externí odkaz:
https://doaj.org/article/8449f4f9d3494bd2a23be8fd5e4fed90
Autor:
Isabel Gugel, Victor-Felix Mautner, Lan Kluwe, Marcos Soares Tatagiba, Martin Ulrich Schuhmann
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Background and Purpose: Neurofibromatosis Type 2 (NF2) is an autosomal-dominant tumor-prone disorder characterized by the manifestations of central nervous system lesions. However, the first clinical signs of disease are often non-tumorous. Cerebrova
Externí odkaz:
https://doaj.org/article/bcbf0f88b00541e19e5883c24102b7f5
Publikováno v:
Journal of Neuro-Oncology. 159:271-279
Introduction Peripheral and intraspinal schwannomas are common and clinically complex pathologies in patients with Neurofibromatosis Type 2 (NF2) and Schwannomatosis (SWNT). Functional preservation and pain relief are the major goals in treating thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1573e11617caa14e336f5c707b9eb3b
https://doi.org/10.1007/s11060-022-04061-0
https://doi.org/10.1007/s11060-022-04061-0
Publikováno v:
Children; Volume 9; Issue 4; Pages: 490
Vestibular schwannomas (VS) usually manifest between the 5th and 8th decade of life. Most pediatric cases are associated with Neurofibromatosis type 2 and sporadic VS are rare in this age group. Few case series have been published. We report on our i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::513864a95fa555d870277439c1411d1f
Autor:
Isabel Gugel, Georgios Naros, Leonidas Trakolis, Felix Leuze, Kathrin Machetanz, Florian Grimm, Marcos Tatagiba, Kristin Mounts
Publikováno v:
Acta Neurochirurgica
Background The semi-sitting position in neurosurgical procedures is still under debate due to possible complications such as venous air embolism (VAE) or postoperative pneumocephalus (PP). Studies reporting a high frequency of the latter raise the qu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::480c1927c00ecc299a8c321db17fe950
http://europepmc.org/articles/PMC7550361
http://europepmc.org/articles/PMC7550361
Autor:
Isabel Gugel, Marcos Tatagiba, Philip Hartjen, Martin U. Schuhmann, Julian Zipfel, Victor-Felix Mautner, Lan Kluwe
Publikováno v:
Child's Nervous System
We reviewed our experience in managing of NF2-associated vestibular schwannoma (VS) in children and young adults regarding the effect of surgery and postoperative bevacizumab treatment. A total of 579 volumetric and hearing data sets were analyzed. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dc817021dc5784615bfcd7d553145de
https://doi.org/10.1007/s00381-020-04728-x
https://doi.org/10.1007/s00381-020-04728-x
Autor:
Lan Kluwe, Martin U. Schuhmann, Florian Grimm, Christian Teuber, Victor-Felix Mautner, Julian Zipfel, Marcos Tatagiba, Isabel Gugel
Publikováno v:
Child's Nervous System
Purpose The hallmark of neurofibromatosis type 2 (NF2) is the presence of bilateral vestibular schwannomas (VS) which however have not yet developed or grown to large size in children and young adolescents. Therefore, early diagnosis in pediatric pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7260db80e24ff4856f0c4a2b60bcc483
https://doi.org/10.1007/s00381-020-04729-w
https://doi.org/10.1007/s00381-020-04729-w
Autor:
Julian Zipfel, Karin Haas-Lude, Martin U. Schuhmann, Isabel Gugel, Victor-Felix Mautner, Steven W. Warmann, Meizer Al-Hariri, Marcos Tatagiba, Michael Krimmel, Alexander Grimm
Publikováno v:
Child's Nervous System
Introduction Peripheral nerve sheath tumours in children are a rare and heterogeneous group, consisting mostly of benign tumours as well as malignant neoplasms. Especially in the paediatric population, diagnostics and indication for therapy pose rele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1720527357d5b11f8318b4015b5b2f36
https://doi.org/10.1007/s00381-020-04703-6
https://doi.org/10.1007/s00381-020-04703-6
Autor:
Martin U. Schuhmann, Karin Haas-Lude, Julian Zipfel, Hagit Toledano-Alhadef, Isabel Gugel, Shlomi Constantini, Victor-Felix Mautner
Publikováno v:
Child's Nervous System
Purpose Neurofibromatosis type 1 (NF1) syndrome is a common rare/orphan disease that manifests itself early in the paediatric age. It imposes a considerable burden upon patients as well as on caregivers. Decisions regarding optimal care often rely on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58a2e5790e887b3449ecb6181287f2dd
http://europepmc.org/articles/PMC7276654
http://europepmc.org/articles/PMC7276654
Publikováno v:
Acta Neurochirurgica. 162:993-1000
In the treatment of childhood hydrocephalus, 3D volumetry seems to have many advantages over classical planar index measurements for dedicated monitoring of changes in cerebrospinal fluid and brain volume. Nevertheless, this method requires extensive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8768f61c0744604f05c9397dedc096f7
https://doi.org/10.1007/s00701-019-04160-4
https://doi.org/10.1007/s00701-019-04160-4