Follow
C Oliver Hanemann
C Oliver Hanemann
Plymouth University Peninsula Medical School
Verified email at plymouth.ac.uk - Homepage
Title
Cited by
Cited by
Year
Placebo-controlled multicentre randomised trial of interferon beta-1b in treatment of secondary progressive multiple sclerosis
Lancet 352 (9139), 1491-1497, 1998
7491998
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS
C Munch, R Sedlmeier, T Meyer, V Homberg, AD Sperfeld, A Kurt, ...
Neurology 63 (4), 724-726, 2004
5302004
Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study
E Nelis, C Van Broeckhoven, P De Jonghe, A Löfgren, A Vandenberghe, ...
European Journal of Human Genetics 4 (1), 25-33, 1996
5171996
The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication
V Timmerman, E Nelis, W Van Hul, BW Nieuwenhuijsen, KL Chen, ...
Nature genetics 1 (3), 171-175, 1992
4501992
Peripheral myelin protein–22 gene maps in the duplication in chromosome 17p11. 2 associated with Charcot–Marie–Tooth 1A
N Matsunami, B Smith, L Ballard, M William Lensch, M Robertson, ...
Nature genetics 1 (3), 176-179, 1992
3721992
Merlin/NF2 suppresses tumorigenesis by inhibiting the E3 ubiquitin ligase CRL4DCAF1 in the nucleus
W Li, L You, J Cooper, G Schiavon, A Pepe-Caprio, L Zhou, R Ishii, ...
Cell 140 (4), 477-490, 2010
3692010
Merlin/NF2 loss-driven tumorigenesis linked to CRL4DCAF1-mediated inhibition of the Hippo pathway kinases Lats1 and 2 in the nucleus
W Li, J Cooper, L Zhou, C Yang, H Erdjument-Bromage, D Zagzag, ...
Cancer cell 26 (1), 48-60, 2014
2472014
Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD
C Münch, A Rosenbohm, AD Sperfeld, I Uttner, S Reske, BJ Krause, ...
Annals of Neurology: Official Journal of the American Neurological …, 2005
2372005
Schwannomas and their pathogenesis
DA Hilton, CO Hanemann
Brain pathology 24 (3), 205-220, 2014
2172014
Axon‐regulated expression of a Schwann cell transcript that is homologous to a ‘growth arrest‐specific’gene.
P Spreyer, G Kuhn, CO Hanemann, C Gillen, H Schaal, R Kuhn, G Lemke, ...
The EMBO journal 10 (12), 3661-3668, 1991
2121991
X-linked bulbospinal neuronopathy: Kennedy disease
AD Sperfeld, J Karitzky, D Brummer, H Schreiber, J Häussler, AC Ludolph, ...
Archives of Neurology 59 (12), 1921-1926, 2002
1992002
DNA methylation profiling to predict recurrence risk in meningioma: development and validation of a nomogram to optimize clinical management
F Nassiri, Y Mamatjan, S Suppiah, JH Badhiwala, S Mansouri, S Karimi, ...
Neuro-oncology 21 (7), 901-910, 2019
1962019
Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria
SR Plotkin, JO Blakeley, DG Evans, CO Hanemann, TJM Hulsebos, ...
American journal of medical genetics Part A 161 (3), 405-416, 2013
1932013
Dissecting and targeting the growth factor–dependent and growth factor–independent extracellular signal-regulated kinase pathway in human schwannoma
S Ammoun, C Flaiz, N Ristic, J Schuldt, CO Hanemann
Cancer research 68 (13), 5236-5245, 2008
1572008
Occurrence and characterization of peripheral nerve involvement in neurofibromatosis type 2
AD Sperfeld, C Hein, JM Schröder, AC Ludolph, CO Hanemann
Brain 125 (5), 996-1004, 2002
1552002
Accumulation of autophagosomes confers cytotoxicity
RW Button, SL Roberts, TL Willis, CO Hanemann, S Luo
Journal of Biological Chemistry 292 (33), 13599-13614, 2017
1522017
Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial
A Al-Chalabi, C Allen, C Counsell, A Farrin, B Dickie, J Kelly
Lancet Neurol 12 (4), 339-45, 2013
1432013
Upregulation of the Rac1/JNK signaling pathway in primary human schwannoma cells
K Kaempchen, K Mielke, T Utermark, S Langmesser, CO Hanemann
Human molecular genetics 12 (11), 1211-1221, 2003
1422003
Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexin 32 mutation
CO Hanemann, C Bergmann, J Senderek, K Zerres, AD Sperfeld
Archives of neurology 60 (4), 605-609, 2003
1422003
Consensus recommendations for current treatments and accelerating clinical trials for patients with neurofibromatosis type 2
JO Blakeley, DG Evans, J Adler, D Brackmann, R Chen, RE Ferner, ...
American journal of medical genetics Part A 158 (1), 24-41, 2012
1342012
The system can't perform the operation now. Try again later.
Articles 1–20