pastille Être découragé Faites un nom mma mut En réalité seau total
JCI Insight - FGF21 underlies a hormetic response to metabolic stress in methylmalonic acidemia
IJMS | Free Full-Text | MCEE Mutations in an Adult Patient with Parkinson's Disease, Dementia, Stroke and Elevated Levels of Methylmalonic Acid | HTML
About Methylmalonic Acidemia
The MRI brain in the child with MUT-related MMA showing predominant... | Download Scientific Diagram
Hepatic Biomarker in MMA - Organic Acidemia Association
The distribution of mutations found in 3 mut-MMA patients. (A) The... | Download Scientific Diagram
Systemic Messenger RNA Therapy as a Treatment for Methylmalonic Acidemia - ScienceDirect
1-13C-propionate breath testing as a surrogate endpoint to assess efficacy of liver-directed therapies in methylmalonic acidemia (MMA) | Genetics in Medicine
Lindsey, MMA Mut 0 - Organic Acidemia Association
mRNA Clinical Trial for MMA Mut 1 Phase 1/2 - Organic Acidemia Association
A critical reappraisal of dietary practices in methylmalonic acidemia raises concerns about the safety of medical foods. Part 1:
Gene expression plot for patients with the MUT form of MMA. MUT mRNA... | Download Scientific Diagram
Methylmalonic and propionic acidemias: clinical management update. - Abstract - Europe PMC
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Metabolic phenotype of methylmalonic acidemia in mice and humans: the role of skeletal muscle | BMC Medical Genetics | Full Text
Long-Term Outcome in Methylmalonic Acidurias Is Influenced by the Underlying Defect (mut0, mut−, cblA, cblB) | Pediatric Research
Frontiers | Newborn Screening for Methylmalonic Acidemia in a Chinese Population: Molecular Genetic Confirmation and Genotype Phenotype Correlations
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia | PNAS
Identification of 2,2-Dimethylbutanoic Acid (HST5040), a Clinical Development Candidate for the Treatment of Propionic Acidemia and Methylmalonic Acidemia | Journal of Medicinal Chemistry
Moderna on Twitter: "Propionic Acidemia (PA) and methylmalonic acidemia (MMA) are #rarediseases that share similar disease pathology & are both typically treated by metabolic specialists. #mRNA https://t.co/k806NfRi7r" / Twitter
Mutation analysis of methylmalonyl CoA mutase gene exon 2 in Egyptian families: Identification of 25 novel allelic variants - ScienceDirect
Methylmalonic acid: an age-related metabolite that drives tumour aggressiveness | Nature Metabolism
MUT - Methylmalonic acidemia due to Mutase deficiency - DHHR
Methylmalonic Acidemia: Symptoms, Causes, Diagnosis, and Treatment
Sarahya and Xayvior, MMA Mut 0 - Organic Acidemia Association
Moderna on Twitter: "The most common form of methylmalonic acidemia (#MMA) is caused by changes in the #MUT gene, which provides instructions for making the MUT enzyme, which is responsible for the