E. Motte

Knock‐In of the Recurrent R368X Mutation of PRKAR1A that Represses cAMP‐Dependent Protein Kinase A Activation: A Model of Type 1 Acrodysostosis

P. Bougnères, E. Clauser, C. Chaussain, 2017, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Mutations causing acrodysostosis‐2 facilitate activation of phosphodiesterase 4D3

N. Dumaz, C. Le Stunff, C. Briet, 2017, Human molecular genetics.

Recurrent PRKAR1A mutation in acrodysostosis with hormone resistance.

P. Chanson, G. Pinto, A. Couvineau, 2011, The New England journal of medicine.

Mitotane (op’DDD) restores growth and puberty in nine children with Cushing’s disease

C. Teinturier, N. Lahlou, A. Rothenbuhler, 2018, Endocrine connections.

Modulation of signaling through GPCR-cAMP-PKA pathways by PDE4 depends on stimulus intensity: Possible implications for the pathogenesis of acrodysostosis without hormone resistance

N. Dumaz, C. L. Stunff, C. Briet, 2017, Molecular and Cellular Endocrinology.

Ketoconazole in Cushing's disease: is it worth a try?

P. Chanson, A. Tabarin, Jacques Young, 2014, The Journal of clinical endocrinology and metabolism.

Translocation (2;8)(p12;q24) associated with a cryptic t(12;21)(p13;q22) TEL/AML1 gene rearrangement in a child with acute lymphoblastic leukemia.

M. Loh, D. Gilliland, S. Sallan, 2000, Cancer genetics and cytogenetics.

Use of neurally adjusted ventilator assist in postsurgical hemidiaphragmatic paralysis

D. De Luca, Yohan Sorèze, N. Yousef, 2017, Archives of Disease in Childhood: Fetal and Neonatal Edition.