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/Tom_Moran_wedding_day_370x280_800_600_s_c1.png)
Thomas’ NF1 story
Thomas describes growing up with NF1, supporting Liverpool FC and taking on challenges with support from his wife
Read More![](https://nervetumours.org.uk/images/made/images/common/Untitled_design_(41)_800_600_s_c1.png)
Meet Jessica, new Specialist NF Nurse
Jessica will work with Specialist NF Nurse Helen Tomkins, supporting families across Devon and Cornwall.
Read More![](https://nervetumours.org.uk/images/made/images/common/fb_eventcover1200_628_-26540595-e1708475536938_800_600_s_c1.png)
Rare Disease Day 2024
Read our update on the events and meetings NTUK attended to help raise awareness of NF
Read More![](https://nervetumours.org.uk/images/made/images/common/77529945_1705140784649954_r__1200x900_with_RDD_logo_1_800_600_s_c1.jpg)
Johnathan’s story
Johnathon's family are spreading awareness of the importance of attending health checks and advocating for vulnerable people
Read More![](https://nervetumours.org.uk/images/made/images/common/image2_(3)_370x280_800_600_s_c1.jpg)
Jen’s NF1 story
Jen praises the great support received since her NF1 diagnosis, allowing her to thrive & achieve a 1st class degree.
Read More![](https://nervetumours.org.uk/images/made/images/common/Untitled_design_(2)_800_600_s_c1.png)
Charlotte & Evie’s story
'Sticker Queen' Evie is 4 years old and was diagnosed with NF1 after tests for a 'lazy eye'.
Read More![](https://nervetumours.org.uk/images/made/images/common/Untitled_design_(5)_800_600_s_c1.png)
Luke’s Story
Luke had NF1 since childhood. Now an adult, surgery last year has enabled him to play football and do whatever he wants
Read More![](https://nervetumours.org.uk/images/made/images/common/Untitled_design_(1)_800_600_s_c1.png)
Charlotte’s Story
When Charlotte was 6, she was diagnosed with NF1, along with her brother & dad. Now she is on a mission to raise awareness
Read More![](https://nervetumours.org.uk/images/made/images/common/cover_image_with_Manchester_Uni_logo_370x280_800_600_s_c1.jpg)
Eden P for healthcare professionals
Healthcare professionals, who provide support to expectant parents with NF1 are invited to take part in the Eden P study
Read More