Expertise in Neurofibromatosis: Within Europe
07 August 2019
Expertise in Neurofibromatosis: Within Europe
Expertscape ( an independent directory dedicated to helping find the top rated professionals and the best areas for care for numerous conditions) has detailed out the relative number of NF expertise by both Country, Region, City, Number of Institutions and Expert rankings within the whole of Europe. This has been based on 1,407 articles published since 2008.
We are proud to announce that the UK is leading the way in Neurofibromatosis expertise with both London and Manchester heavily contributing towards the number of experts and research surrounding NF.
Professor Gareth Evans also tops the list as the top rated NF expert in the whole of Europe with our own Professor Rosalie Ferner coming in 3rd!
Other experts listed and involved in UK treatment and support to those who have NF are Doctor Sue Huson, Professor Meena Upadhyaya, Professor Oliver Hanemann and Professor Andrew King. All of these are acitve on our Medical Advisory Board.
For the complete list make sure to click on the link below:
Professor Gareth Evans
![](/images/made/images/common/gareth_evans_2_1024_768_s_c1.jpg)
Professor Rosalie Ferner
![](/images/made/images/common/Rosalie_Ferner_1024_768_s_c1.jpg)
Filter News
![](https://nervetumours.org.uk/images/made/images/common/robina-weermeijer-3KGF9R_0oHs-unsplash_370x280_800_600_s_c1.jpg)
NF1 stem cell research study
Julieta is carrying out stem cell research to understand brain development in those with NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/FB_IMG_1646043328094_370x280_800_600_s_c1.jpg)
Ava-Lily’s NF1 story
Ava-Lily is thriving at school despite various NF1 related difficulties - read her story
Read More![](https://nervetumours.org.uk/images/made/images/common/image_(12)_370x280_800_600_s_c1.jpg)
Westminster Virtual Rare Disease Day 2022 Reception
NTUK joined the annual international event aimed at raising awareness & highlighting the needs of people with rare diseases
Read More![](https://nervetumours.org.uk/images/made/images/common/NTUK_supports_RDD_370x280_800_600_s_c1.jpg)
Rare Disease Day 2022
Nerve Tumours UK joins events showcasing Rare Disease Day, hosted by the Genetic Alliance, on 28 February 2022
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_7612_370x280_800_600_s_c1.jpg)
Runderpants Winchester 2022
The Runderpants fun run makes a successful return to Winchester
Read More![](https://nervetumours.org.uk/images/made/images/common/fruit_fly_370x280_800_600_s_c1.jpg)
NF1 Research study with fly model
How can studying the brain of a fruit fly help with understanding of NF1?
Read More![](https://nervetumours.org.uk/images/made/images/common/2021-10-27_15-11-36_324_370x280_800_600_s_c1.jpg)
Stuart’s Schwannoma Story Part Two
Stuart's update takes us through the operation to remove the Schwannoma, recovery and getting back to marathon training.
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_4619_370x280_800_600_s_c1.jpg)
Sian & Connor’s story
Sian & Connor describe the invaluable support from NTUK during her pregnancy with baby Reuben
Read More![](https://nervetumours.org.uk/images/made/images/common/17397DC99F38479194C0E2ADD6B8CDA8_370x280_800_600_s_c1.jpg)
Anita, aka Fat Lady Slim, is running the London Marathon for NTUK
Anita is fundraising on behalf of niece Sophie & great-niece Lexie who have NF2 by running the London Marathon
Read More