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Administration of gamma‐hydroxybutyrate instead of beta‐hydroxybutyrate to a liver transplant recipient suffering from propionic acidemia and cardiomyopathy: A case report on a medication prescribing error.
Published in:
Journal of Inherited Metabolic Disease Reports, 2020, v. 51, n. 1, p. 25, doi. 10.1002/jmd2.12090
By:
- Tuchmann‐Durand, Caroline;
- Thevenet, Eloise;
- Moulin, Florence;
- Lesage, Fabrice;
- Bouchereau, Juliette;
- Oualha, Mehdi;
- Khraiche, Diala;
- Brassier, Anaïs;
- Wicker, Camille;
- Gobin‐Limballe, Stéphanie;
- Arnoux, Jean‐Baptiste;
- Lacaille, Florence;
- Wicart, Clotilde;
- Coat, Bruno;
- Schlattler, Joel;
- Cisternino, Salvatore;
- Renolleau, Sylvain;
- Secretan, Philippe‐Henri;
- De Lonlay, Pascale
Publication type:
Article
OTC deficiency in females: Phenotype‐genotype correlation based on a 130‐family cohort.
Published in:
Journal of Inherited Metabolic Disease, 2021, v. 44, n. 5, p. 1235, doi. 10.1002/jimd.12404
By:
- Gobin‐Limballe, Stephanie;
- Ottolenghi, Chris;
- Reyal, Fabien;
- Arnoux, Jean‐Baptiste;
- Magen, Maryse;
- Simon, Marie;
- Brassier, Anaïs;
- Jabot‐Hanin, Fabienne;
- Lonlay, Pascale De;
- Pontoizeau, Clement;
- Guirat, Manel;
- Rio, Marlene;
- Gesny, Roselyne;
- Gigarel, Nadine;
- Royer, Ghislaine;
- Steffann, Julie;
- Munnich, Arnold;
- Bonnefont, Jean‐Paul
Publication type:
Article