Intermittent hemophagocytic lymphohistiocytosis is a regular feature of lysinuric protein intolerance
Michel Duval(Inserm), E Vilmer(Hôpital Robert-Debré), Ghislaine Sterkers(Délégation Paris 7), Patricia Yotnda(Baylor College of Medicine), Odile Fenneteau(Assistance Publique – Hôpitaux de Paris), Hélène Ogier de Baulny(Université Paris Cité), Dominique Émilie(Inserm), Jean‐Claude Drapier(Centre National de la Recherche Scientifique), Albert Faye(Inserm), V. Doireau(Inserm), Nicole Schlegel(Inserm)
Cited by 116
Related Papers
Outcome of treatment in childhood acute lymphoblastic leukaemia with rearrangements of the 11q23 chromosomal region
|The Lancet|2002|401
Fatty Acid Oxidation-Driven Src Links Mitochondrial Energy Reprogramming and Oncogenic Properties in Triple-Negative Breast Cancer
|Cell Reports|2016|320
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation
|Journal of Inherited Metabolic Disease|2015|248
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype
|Journal of Inherited Metabolic Disease|2015|236