#Legius
Hello! Newly diagnosed with a #RASopathy syndrome? (#Noonan, #Costello, #Cardiofaciocutaneous #CFCsyndrome, #Neurofibromatosis 1, #Legius, and others) ⬇️ Here's a helpful whiteboard video to explain more youtu.be/-ZbyIWLVTds?...
What are the RASopathies (updated)
YouTube video by RASopathies Network Videos
youtu.be
November 25, 2024 at 8:21 PM
J.S.Bach: Trio Sonata in G major, BWV 1038 (Musica Antiqua Köln, Reinhard Goebel) www.youtube.com/watch?v=oFC3... #classicalmusic
J.S.Bach: Trio Sonata in G major, BWV 1038 (Musica Antiqua Köln, Reinhard Goebel)
YouTube video by Legius N.
www.youtube.com
May 4, 2025 at 8:39 AM
Ons ma wordt zo al +10 jaar onderzocht. Tegenwoordig automatisch zelfs, door professor Legius (1x jaar buisjes bloed). En dan krijgt ze een brief dat ze blijven zoeken en dat het belangrijk is dat wij (kinderen) preventief op controle gaan.
3 types kanker in 1 persoon is iets te veel toeval.
January 6, 2025 at 4:38 PM
Earn 1 CME credit with our accredited podcast series, Unpacking NF1 Care. Listen to Eric Legius, Rosalie Ferner, and Mandy Myers explore strategies to support independence, build self-management skills, and ensure continuity of care throughout adolescence and beyond

https://ow.ly/T5A250Zw85N
August 6, 2026 at 10:00 AM
I'll be honest I forgot Legius was in this show he stopped doing anything like 15 episodes ago
May 8, 2026 at 12:27 PM
I save them for later. Like you re religion and “doing” Christmas.
Add on Hely-Hutchinson’s Carol
symphony and for a really quirky one, m.youtube.com/watch?v=urt9...
Edmund Pascha: Christmas Mass - Carols (Prague Madrigal Singers 1969)
YouTube video by Legius N.
m.youtube.com
December 1, 2024 at 3:15 PM
@thermofishersci.bsky.social's resource, RRID:AB_2576217, was just reported to be used in the paper. Thanks for making your methods matter! #OpenResearch #accelerateopenscience #OpenScience
Generation and characterization of four iPSC and isogenic gene-corrected lines from Legius syndrome patients
Read the full paper: Generation and characterization of four iPSC and isogenic gene-corrected lines from Legius syndrome patients
doi.org
June 19, 2026 at 7:00 AM
Listen to our accredited podcast, Unpacking NF1 Care, to hear Eric Legius and Ignacio Blanco discuss applying NF1 therapies in real-world practice, patient selection, treatment considerations, and strategies to optimize outcomes
https://ow.ly/EEpT50ZIjp5
September 2, 2026 at 4:01 PM
What should lifelong, proactive NF1 care look like? Eric Legius and Ignacio Blanco explore evolving surveillance strategies, multidisciplinary care, psychosocial support, digital health tools, and guideline-driven care
https://ow.ly/VGxe50Zwb3v

Listen to the full podcast series to earn 1 CME credit
August 10, 2026 at 2:01 PM
Listen to our NEW accredited podcast, Unpacking NF1 Care, to hear Eric Legius and Ignacio Blanco discuss applying NF1 therapies in real-world practice, patient selection, treatment considerations, and strategies to optimize outcomes

https://ow.ly/Pf3l50ZmPV1
July 13, 2026 at 2:01 PM
Ametis amelia putri legius
June 11, 2024 at 11:51 AM
UAB is the go to for genetic testing for NF1/Legius syndrome. Messing with their research budget will mess with healthcare across the nation, I'm thinking.
February 9, 2025 at 9:25 PM
In voor- en regenspoed. #taalvout

(Met dank aan Marja Legius!)
August 4, 2025 at 4:00 AM
Lianne en zoon Stijn (6) leven met zeldzaam Legius-syndroom: ‘De winter is hels’

Lianne Verheij-Oelbers (37) was accountmanager met een druk leven, totdat ze op haar 32ste de diagnose kreeg: het Legius-syndroom, een zeldzame aandoening waarbij hersensignalen het lichaam niet goed bereiken....
Lianne en zoon Stijn (6) leven met zeldzaam Legius-syndroom: ‘De winter is hels’
Lianne Verheij-Oelbers (37) was accountmanager met een druk leven, totdat ze op haar 32ste de diagnose kreeg: het Legius-syndroom, een zeldzame aandoening waarbij hersensignalen het lichaam niet goed ...
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April 28, 2026 at 12:10 PM
Stijn (6) heeft dezelfde zeldzame aandoening als zijn moeder: ‘Hij heeft het van mij, dat is heel moeilijk’

Lianne Verheij-Oelbers (37) was accountmanager met een druk leven, totdat ze op haar 32ste de diagnose kreeg: het Legius-syndroom, een zeldzame aandoening waarbij hersensignalen het...
Stijn (6) heeft dezelfde zeldzame aandoening als zijn moeder: ‘Hij heeft het van mij, dat is heel moeilijk’
Lianne Verheij-Oelbers (37) was accountmanager met een druk leven, totdat ze op haar 32ste de diagnose kreeg: het Legius-syndroom, een zeldzame aandoening waarbij hersensignalen het lichaam niet goed ...
www.ad.nl
April 28, 2026 at 11:48 AM
Legius Syndrome
Legius Syndrome
Legius Syndrome
pubmed.ncbi.nlm.nih.gov
December 21, 2025 at 10:13 PM
Legius Syndrome
Legius Syndrome
Legius Syndrome
pubmed.ncbi.nlm.nih.gov
December 21, 2025 at 4:13 PM
Legius Syndrome
Legius Syndrome
Legius Syndrome
pubmed.ncbi.nlm.nih.gov
December 21, 2025 at 10:13 AM
Legius Syndrome
Legius Syndrome
Legius Syndrome
pubmed.ncbi.nlm.nih.gov
December 21, 2025 at 3:13 AM
Legius Syndrome
Legius Syndrome
Legius Syndrome
pubmed.ncbi.nlm.nih.gov
December 21, 2025 at 1:15 AM
Significance of the Absence of Focal Areas of Signal Intensity on Brain Magnetic Resonance Imaging Examinations in Legius Syndrome
Significance of the Absence of Focal Areas of Signal Intensity on Brain Magnetic Resonance Imaging Examinations in Legius Syndrome
Significance of the Absence of Focal Areas of Signal Intensity on Brain Magnetic Resonance Imaging Examinations in Legius Syndrome
pubmed.ncbi.nlm.nih.gov
June 15, 2025 at 8:57 AM
Functional Assays Combined with Pre-mRNA-Splicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius Syndrome
Functional Assays Combined with Pre-mRNA-Splicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius Syndrome
Functional Assays Combined with Pre-mRNA-Splicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius Syndrome
pubmed.ncbi.nlm.nih.gov
April 14, 2025 at 4:57 PM
Legius Syndrome: the importance of molecular differential diagnosis with neurofibromatosis type 1
Legius Syndrome: the importance of molecular differential diagnosis with neurofibromatosis type 1
Legius Syndrome: the importance of molecular differential diagnosis with neurofibromatosis type 1
pubmed.ncbi.nlm.nih.gov
April 2, 2025 at 4:57 PM