![Methylmalonic Aciduria — An Inborn Error Leading to Metabolic Acidosis, Long-Chain Ketonuria and Intermittent Hyperglycinemia | NEJM Methylmalonic Aciduria — An Inborn Error Leading to Metabolic Acidosis, Long-Chain Ketonuria and Intermittent Hyperglycinemia | NEJM](https://www.nejm.org/na101/home/literatum/publisher/mms/journals/content/nejm/1968/nejm_1968.278.issue-24/nejm196806132782404/20130815/images/img_medium/nejm196806132782404_f1.jpeg)
Methylmalonic Aciduria — An Inborn Error Leading to Metabolic Acidosis, Long-Chain Ketonuria and Intermittent Hyperglycinemia | NEJM
![Pathways for Hcy and MMA metabolism in humans. (A) Homocysteine is a... | Download Scientific Diagram Pathways for Hcy and MMA metabolism in humans. (A) Homocysteine is a... | Download Scientific Diagram](https://www.researchgate.net/publication/304491813/figure/fig1/AS:378215160926208@1467184929715/Pathways-for-Hcy-and-MMA-metabolism-in-humans-A-Homocysteine-is-a-branch-point.png)
Pathways for Hcy and MMA metabolism in humans. (A) Homocysteine is a... | Download Scientific Diagram
Article: Association of vitamin B12, methylmalonic acid, and functional parameters (full text) - February 2020 - NJM
![Guidelines for the diagnosis and management of methylmalonic acidaemia and propionic acidaemia: First revision - Forny - 2021 - Journal of Inherited Metabolic Disease - Wiley Online Library Guidelines for the diagnosis and management of methylmalonic acidaemia and propionic acidaemia: First revision - Forny - 2021 - Journal of Inherited Metabolic Disease - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/74f40b56-55af-4ead-829b-1e2b4c966562/jimd12370-fig-0001-m.jpg)
Guidelines for the diagnosis and management of methylmalonic acidaemia and propionic acidaemia: First revision - Forny - 2021 - Journal of Inherited Metabolic Disease - Wiley Online Library
![Methylmalonic acidemia/propionic acidemia – the biochemical presentation and comparing the outcome between liver transplantation versus non-liver transplantation groups | Orphanet Journal of Rare Diseases | Full Text Methylmalonic acidemia/propionic acidemia – the biochemical presentation and comparing the outcome between liver transplantation versus non-liver transplantation groups | Orphanet Journal of Rare Diseases | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13023-019-1045-1/MediaObjects/13023_2019_1045_Fig1_HTML.png)