Cynthia Le Mons

Evaluation of neurocognitive function of prefrontal cortex in ornithine transcarbamylase deficiency.

A. Gandjbakhche, C. Stratakis, A. Gropman, 2020, Molecular genetics and metabolism.

Hemodynamics of Prefrontal Cortex in Ornithine Transcarbamylase Deficiency: A Twin Case Study

A. Gandjbakhche, C. Stratakis, A. Gropman, 2020, Frontiers in Neurology.

Choosing between medical management and liver transplant in urea cycle disorders: A conceptual framework for parental treatment decision‐making in rare disease

A. Markus, C. Le Mons, N. Mew, 2019, Journal of inherited metabolic disease.

Protein and calorie intakes in adult and pediatric subjects with urea cycle disorders participating in clinical trials of glycerol phenylbutyrate☆

Ingrid L. Rudolph-Angelich, N. Longo, Brendan H. Lee, 2016, Molecular genetics and metabolism reports.

ASL expression in ALDH1A1+ neurons in the substantia nigra metabolically contributes to neurodegenerative phenotype

M. Tuchman, M. Baumgartner, S. Waisbren, 2021, Human Genetics.

Barriers to a successful healthcare transition for individuals with urea cycle disorders.

W. Craigen, R. Marom, P. Magoulas, 2023, Molecular genetics and metabolism.

The incidence of urea cycle disorders.

Hye-Seung Lee, J. Haberle, M. Summar, 2013, Molecular genetics and metabolism.