Top Tweets for #GDMCC
This study from @UNCChildrens and the #GDMCC found children with PCD and abnormal organ arrangement have worse nutritional and pulmonary outcomes, more hospitalizations, and higher incidence of cardiovascular and splenic anomalies. #PCD @rarediseasesnet
https://t.co/5uAIZLPlt2
If you don’t catch me #ATSPAR come see the #GDMCC @rarediseasesnet noontime Sunday and catch me at the @nih_nhlbi booth ~1:30 pm Sunday.
Read about what our PCD research partners are doing to better understand PCD and how current studies will help contribute to clinical trial readiness. Features a PCDF Board Director- Tori Eastvold.
https://t.co/HDM91tbOpl
#pcd #primaryciliarydyskinesia #GDMCC #RDCRN
#GDMCC @rarediseasesnet is seeking applicants for the @PCDFoundation Margaret W. Leigh Early Career Investigator Award. Applications due November 15, 2023. https://t.co/BjyuBY80uK
Findings suggest that airway inflammation may be a target for therapeutic intervention in people with PCD.
#gdmcc #primaryciliarydyskinesia #mucociliary
https://t.co/s56STC7jrI
#RareDiseasesChat #RDDNIH Primary Ciliary Dyskinesia is another #RareDisease @nih_nhlbi @NHLBI_LUNGDir supports research. check out the @rarediseasesnet #GDMCC or reach out to the @PCDFoundation for more information. https://t.co/bEnTID0v4x
Investigating the Role of #AirwayInflammation in Children with #PrimaryCiliaryDyskinesia
New in @AnnalsATS from the Genetic Disorders of #MucociliaryClearance Consortium (#GDMCC): https://t.co/48Db3u6cqS
More from our CRCN GDMCC trainee meeting. Updates from our international colleagues- it truly takes a village! #CRCN #ATS2022 #primaryciliarydyskinesia #gdmcc @Shoemelia
Advancing Discoveries in #Mucociliary Clearance Diseases ➡️ Stephanie Davis, MD, and Thomas Ferkol, MD, share the history of the #GDMCC, current research, and future plans: https://t.co/nKn7fpEHVg
#RDCRN #PrimaryCiliaryDyskinesia #CysticFibrosis #PrimaryImmunodeficiencies
The #GDMCC is part of the #RDCRN, with focus on disorders of mucociliary clearance such as primary ciliary dyskinesia #PCD and primary immune deficiencies partnering with @PCDFoundation @PrimaryImmuno groups. #nihchat #rdd
When you have a rare disease, every day is Rare Disease Day. Every day, you have to teach someone new about what you have. Patient advocacy groups work to provide informational resources to people living with rare diseases. Connect with ours at https://t.co/4w0tOSVPnb #NIHchat
Emerging #Genotype-#Phenotype Relationships in #PrimaryCiliaryDyskinesia: Genetic panels for PCD reveal milder forms of disease that had previously gone unrecognized
New review in @IJMS_MDPI w/Genetic Disorders of #Mucociliary Clearance Consortium #GDMCC: https://t.co/ggvm3OKp6u
New from our Genetic Disorders of Mucociliary Clearance Consortium #GDMCC: Autosomal dominant variants in FOXJ1 causing primary ciliary dyskinesia #PCD in two patients with obstructive hydrocephalus https://t.co/E1kr71FHXx
@UNC_SOM @HeterotaxyOrg @IDFCommunity @PCDFoundation
Using #WholeExomeSequencing and #bioinformatic analysis, researchers from @rarediseasesnet's Genetic Disorders of #Mucociliary Clearance Consortium (#GDMCC) discovered a new gene causing #PrimaryCiliaryDyskinesia, as published in @PLOSGenetics. Read more: https://t.co/UNTpsILr12
What is the genetic cause behind impaired #mucociliary clearance of the lungs? Researchers from #RDCRN's Genetic Disorders of Mucociliary Clearance Consortium (#GDMCC) contributed to the discovery of a new disease gene, NEK10, that regulates #cilia length: https://t.co/iAKdAyzSwI
A novel disease gene, NEK10, causes impaired mucociliary clearance of the lungs in study led by Raghu Chivukula @chivukula_raghu w/ #RDCRN #GDMCC.
➡️ Potential implications for #CysticFibrosis, #PCD, & others
Study: https://t.co/bkuVZlPzhX
Article: https://t.co/e9Cy7F6Fgu
#RDDNIH Session on Diagnostic Odyssey is about to start. Dr. Knowles from #RDCRN #GDMCC @rarediseasesnet will be speaking on using the EHR to mine for undiagnosed rare diseases patients. #rarediseaseday2020 #rarediseases
The #GDMCC is part of this group with #PCD, #PID and non-CF #bronchiectasis. Some patient advocacy partners @PCDFoundation @IDFCommunity and more, visit @rarediseasesnet for info.
#20DaysofRareDiseaseResearch
1/ Today, we are highlighting the Genetic Disorders of #Mucociliary #Clearance Consortium #GDMCC, one of the oldest #RDCRN teams. Follow this thread to learn about the disorders they study, their team and their research plans https://t.co/mbCuHIqqoT
What words come to mind when you think of the patient advocacy groups you work with? Here’s some from crowdsourcing #RDCRN2019 #gdmcc @HeterotaxyOrg @COPDFoundation @PCDFoundation @rarediseasesnet
5/ Stephanie Davis, MD of UNC Chapel Hill @UNC_SOM is #GDMCC's primary investigator. Patient advocacy group partners include:
@CF_Foundation
@PCDFoundation
@NTMinfo
@COPDFoundation
@HeterotaxyOrg
Jeffrey Modell Foundation @dosomethingdoc
@IDFCommunity
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