Zobrazeno 1 - 10
of 12
pro vyhledávání: '"C. O. Hanemann"'
Autor:
L, Provenzano, Y, Ryan, D A, Hilton, J, Lyons-Rimmer, F, Dave, E A, Maze, C L, Adams, R, Rigby-Jones, S, Ammoun, C O, Hanemann
Publikováno v:
Oncogene. 36(44)
Loss of function mutations in the neurofibromatosis Type 2 (NF2) gene, coding for a tumour suppressor, Merlin, cause multiple tumours of the nervous system such as schwannomas, meningiomas and ependymomas. These tumours may occur sporadically or as p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ebbc5112d2a9660686c2bbf69e31773f
https://pubmed.ncbi.nlm.nih.gov/28692055
https://pubmed.ncbi.nlm.nih.gov/28692055
Publikováno v:
Neuropathology and applied neurobiology. 38(6)
Δ⁹-tetrahydrocannabinol (Δ⁹-THC) is neuroprotective in models of Parkinson's disease (PD). Although CB1 receptors are increased within the basal ganglia of PD patients and animal models, current evidence suggests a role for CB1 receptor-indepen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad6a6319f8baf3ce61ae92002e76d666
https://pubmed.ncbi.nlm.nih.gov/22236282
https://pubmed.ncbi.nlm.nih.gov/22236282
Publikováno v:
Der Nervenarzt. 78(4)
Central core myopathy is a nonprogressive or only slowly progressive congenital muscle disease. In most cases, symptoms begin in childhood, but rare cases with adult onset are described. Regardless of its high variability, the clinical hallmarks are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e158744df5b6b312a898c92c998be40
https://pubmed.ncbi.nlm.nih.gov/17235422
https://pubmed.ncbi.nlm.nih.gov/17235422
Publikováno v:
Journal of neuroscience research. 61(5)
Neurofibromas are benign tumors arising from the peripheral nerve sheath and are a typical finding in neurofibromatosis type 1 (NF1). Schwann cells are the predominant cell type in neurofibromas and thus are supposed to play a major role in the patho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cb241db2671c67309c1803b279b0d39c
https://pubmed.ncbi.nlm.nih.gov/10956422
https://pubmed.ncbi.nlm.nih.gov/10956422
Autor:
M, Kamleiter, C O, Hanemann, L, Kluwe, C, Rosenbaum, S, Wosch, V F, Mautner, H W, Müller, P, Grafe
Publikováno v:
Glia. 24(3)
Previous experimental observations indicate that inhibition of voltage-dependent K+ currents suppresses proliferation of normal Schwann cells. In the present study we tested the opposite relationship, i.e., whether Schwann cells from tumors with abno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::89c2dbbd6e239e50aac9cf893230fa6d
https://pubmed.ncbi.nlm.nih.gov/9775982
https://pubmed.ncbi.nlm.nih.gov/9775982
Publikováno v:
Musclenerve. 21(11)
This study examined major histocompatibility complex (MHC) class II expression and macrophage infiltration in sural nerve biopsies from patients with genetically proven Charcot-Marie-Tooth (CMT) 1A and 1B and hereditary neuropathy with liability to p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7a20ceb22bc9b87973bfe0cefa867eca
https://pubmed.ncbi.nlm.nih.gov/9771665
https://pubmed.ncbi.nlm.nih.gov/9771665
Publikováno v:
Glia. 23(2)
A duplication of the gene for myelin protein PMP22 is by far the most common cause of the hereditary demyelinating neuropathy CMT1A. A role for PMP22 in cell growth in addition to its function as a myelin protein has been suggested because PMP22 is h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc93f8c048fa11153f7160a0cd209a3a
https://pubmed.ncbi.nlm.nih.gov/9600378
https://pubmed.ncbi.nlm.nih.gov/9600378
Publikováno v:
Glia. 21(3)
Previous studies have shown that Schwann cell implantation offers a potential therapeutic approach to a variety of neurodegenerative disorders and traumatic injuries. In a clinically relevant paradigm, however, the implantation of autologous Schwann
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a6b62a9ff85df40292af6452de58e73
https://pubmed.ncbi.nlm.nih.gov/9383039
https://pubmed.ncbi.nlm.nih.gov/9383039
Autor:
R, Korinthenberg, M, Sauer, U P, Ketelsen, C O, Hanemann, G, Stoll, M, Graf, A, Baborie, B, Volk, B, Wirth, S, Rudnik-Schöneborn, K, Zerres
Publikováno v:
Annals of neurology. 42(3)
Three newborn siblings presented with generalized weakness, asphyxia, facial diplegia, and external ophthalmoplegia. Electrophysiological testing showed inexcitability of motor and sensory nerves and myographic signs of denervation. Nerve biopsies an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a6a4f2a6ab0efccf6f95ab63dfccc35e
https://pubmed.ncbi.nlm.nih.gov/9307259
https://pubmed.ncbi.nlm.nih.gov/9307259
Autor:
H W, Müller, U, Suter, C, Van Broeckhoven, C O, Hanemann, E, Nelis, V, Timmerman, S, Sancho, L, Barrio, P, Bolhuis, R, Dermietzel, M, Frank, A, Gabreëls-Festen, C, Gillen, N, Haites, G, Levi, E, Mariman, R, Martini, K, Nave, B, Rautenstrauss, M, Schachner, A, Schenone, C, Schneider, M, Schröder, K, Willecke, O, Haneman
Publikováno v:
Neurobiology of disease. 4(3-4)
The First Workshop of the European Consortium on Charcot-Marie-Tooth (CMT) disease brought together neuroscientists, molecular and cell biologists, neuropathologists, neurologists, and geneticists with a common interest in the understanding of the fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e8c9489025e6820b5fffae2eefec6797
https://pubmed.ncbi.nlm.nih.gov/9361297
https://pubmed.ncbi.nlm.nih.gov/9361297