Top Tweets for #LCFAOD
Human VLCAD (hVLCAD) #mRNA can reverse the metabolic effects of VLCAD deficiency a type of
#LongChainFattyAcidOxidationDisorder (#LCFAOD) & generate functional very long-chain acyl-CoA dehydrogenase (VLCAD) enzyme in cell culture.
Read more: https://t.co/PUuwlyNr3S
#MedEd

The #COVID19 pandemic negatively affected the #MentalHealth of people with #RareDiseases; especially people affected by #InheritedMetabolicDiseases such as #LCFAOD, even though these patients showed better #QualityOfLife. Study in MGM Reports @SIMDtweets https://t.co/8PBbyYAQwa
A 14-year-old male patient was diagnosed with cooccurring type 1 diabetes mellitus (DM1) and very long chain acyl-CoA dehydrogenase deficiency (VLCADD), a type of #LongChainFattyAcidOxidationDisorder (#LCFAOD). Case report in @Clin_Biochem.
Read more: https://t.co/7DjgDavi9D
#Tryptophan metabolites and medium- and #LongChainFattyAcids are altered in patients with major depressive disorder and schizophrenia. Study in @MdpiMedicina.
Read more: https://t.co/ot39SswtoV
#LongChainFattyAcidOxidationDisorder #LCFAOD
It's #RareDiseaseDay! Recently, Dr. Aziz Mhanni spoke w/ @patientvoiceca about a group of rare, life-altering metabolic conditions known as long-chain fatty acid oxidation disorders (LCFAOD).
More about #LCFAOD, and their impact on quality of life here: https://t.co/NLBsp9639C
#Mavodelpar receives #FastTrack Designation from the @US_FDA for #LongChainFattyAcidOxidationDisorder (#LCFAOD). Press release from @ReneoPharma.
Read more here: https://t.co/awt7Mc1JfZ
#FattyAcidOxidationDisorder #GeneticDisease #MedNews
We spoke with @CHRIManitoba's Dr. Aziz Mhanni to learn about a group of rare, life-altering metabolic conditions known as long-chain fatty acid oxidation disorders (#LCFAOD). He discusses symptomology, management and impact on patient/caregiver QOL. https://t.co/56vvGHCwee
Andrew was diagnosed with #LCHAD, a type of long-chain fatty acid oxidation disorder (#LCFAOD), at six months old. He’s had to adapt almost every aspect of his life, but one thing remains constant — a passion for baseball. Story below. With @mitocanada. https://t.co/kylsO0t4TV
#Icariin can improve #FattyAcidOxidation and reduce the accumulation of #lipids in the liver, according to a new study published in the journal @Molecules_MDPI.
Read more here: https://t.co/WgsowSb8bn
#LongChainFattyAcidOxidationDisorder #LCFAOD

There is a lack of scientific consensus on whether #CarnitinePalmitoyltransferase2Deficiency should be offered as part of a #NewbornScreening program. https://t.co/dNLnHhbXdS #MedTwitter #FAOD #FattyAcidOxidationDisorder #LCFAOD #CardioTwitter #RareDisease
#Caregivers like Christy play a critical role helping to meet the needs of their loved ones living with #RareDiseases. Despite the challenges they face every day, caregivers remain committed to those who are counting on them. This #NFCMonth, we recognize all caregivers. #LCFAOD

My story on how Eileen Sullivan Baker began advocating for patients with long-chain fatty acid oxidation disorder. #LCFAOD @ultragenyx @MitoAction @RareDisease @GlobalLiver @RareDisease_Adv @LDRTC_USA @foundationofnla @IJNS_MDPI @Jeevatrials @UMDFScience https://t.co/WRFGyr3G95
Our therapy that treats long chain fatty acid oxidation disorders (#LCFAOD) has been approved for children and adults with this condition in Mexico by COFEPRIS, the federal regulatory agency. Ultragenyx’s team in Mexico recently gathered to celebrate.
#MitochondrialDiseases

New 'Accepted Article'
Genetic, biochemical and clinical spectrum of patients with mitochondrial trifunctional protein deficiency identified after introduction of newborn screening in the Netherlands
Marit Schwantje, @TGJDerks @rhhoutkooper et al
https://t.co/d2dQyT777A
#LCFAOD

New #openaccess content in #JIMDReports
Genotype–phenotype correlations in CPT1A deficiency detected by newborn screening in Pacific populations
Isaac Bernhardt, et al
https://t.co/GrLlsrBUTc
#FAOD #LCFAOD

The paper that was just referenced is available #openaccess (from another journal!)
#triheptanoin #LCFAOD
https://t.co/QlUgrIuGRk
My story in #RareDiseaseAdvisor on #LCFAOD (long-chain fatty acid oxidation disorder). @RareDisease_Adv @GlobalLiver @LDRTC_USA #LiverDisease @dcpatient @RareDiseases @foundationofnla @AlexionPharma @ultragenyx @IJNS_MDPI @CorrieTimmer @UMDFScience https://t.co/skD6YqilyA
MSL DAILY PHARMA NEWS - FDA backs second rare disease drug from Ultragenyx in the space of a fortnight
#Ultragenyx #Dojolvi #LCFAOD
“the body is unable to convert long-chain fatty acids into energy”
#MSL #FSTP #MSLcert #medicalscienceliaison
https://t.co/VVVuU7204L
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