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2018 Australasian Neurofibromatosis Conference

Children's Tumour Foundation of Australia

Friday, 21 September 2018 from 8:30 am to 6:00 pm (AEST)

2018 Australasian Neurofibromatosis Conference

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Ticket Type Sales End Price * Fee Quantity
Early Bird - Registration Ended $55.00 $0.00
Early Bird - Group   more info Ended $41.00 $0.00
* Prices include GST

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Event Details

The Children's Tumour Foundation of Australia warmly invites you to:

The 2nd Australasian Neurofibromatosis Conference 2018

We are proud to announce the 2nd Australasian Neurofibromatosis Conference to be held in Melbourne.

The conference will feature a keynote address from Doctor Bruce Korf MD, PhD, who is one of the leading clinical experts and researchers in the field of neurofibromatosis. The address will be followed by presentations outlining the latest clinical thinking on research findings and treatment approaches for patients diagnosed with Neurofibromatosis (NF).

Our aim is to bring together clinicians and researchers to improve collaboration in this diverse clinical community.



DATE: Friday 21 September 2018

WHERE: Level 5 MCRI – Cox/Walford seminar room
The Royal Children’s Hospital
50 Flemington Road, Parkville VIC 3052



PLEASE NOTE: This event is exclusively for Doctors, Clinical Specialists, Scientists and Researchers in the field of Neurofibromatosis.


Have questions about 2018 Australasian Neurofibromatosis Conference? Contact Children's Tumour Foundation of Australia

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When & Where

Level 5 MCRI – Cox/Walford seminar room
The Royal Children's Hospital, Melbourne
50 Flemington Road
Parkville, VIC 3052

Friday, 21 September 2018 from 8:30 am to 6:00 pm (AEST)

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Children's Tumour Foundation of Australia

The Children's Tumour Foundation is a not-for-profit organisation dedicated to providing information, resources and support services to children, their families and adults living with neurofibromatosis (NF), a term for three distinct disorders: NF1, NF2 and schwannomatosis. CTF also raises funds to support promising medical research aimed at finding new treatments and ultimately a cure for NF.

NF1 is one of the most common genetic inherited conditions, affecting up to 1 in 2,500 individuals. It is at least as common as Cystic Fibrosis, Muscular Dystrophy and Huntington's disease, yet there is little community awareness and significant gaps in health services for the NF community across the country.

CTF is committed to ensuring those suffering with NF receive adequate, multidisciplinary care throughout their lives.

CTF has strong links internationally to NF organisations and researchers in the USA, Great Britain, Ireland, Canada and Europe.  We also work closely and provide funding to world-class local researchers and clinicians at The Children's Hospital at Westmead, the Murdoch Children's Research Institute and Royal North Shore Hospital.

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