2017 D. Herzig, P. Eser, T. Radtke, A. Wenger, T. Rusterholz, M. Wilhelm, P. Achermann, A. Arhab, O. G. Jenni, T. H. Kakebeeke, C. S. Leeger-Aschmann, N. Messerli-Burgy, A. H. Meyer, S. Munsch, J. J. Puder, E. A. Schmutz, K. Stulb, A. E. Zysset and S. Kriemler, Relation of Heart Rate and its Variability during Sleep with Age, Physical Activity, and Body Composition in Young Children, Front Physiol, 8 pp109, 2017. Pubmed

2017 D. G. Sweet, V. Carnielli, G. Greisen, M. Hallman, E. Ozek, R. Plavka, O. D. Saugstad, U. Simeoni, C. P. Speer, M. Vento, G. H. Visser and H. L. Halliday, European Consensus Guidelines on the Management of Respiratory Distress Syndrome - 2016 Update, Neonatology, 111 (2), pp107-125, 2017 Pubmed

2017 D. E. Whittaker, K. L. Riegman, S. Kasah, C. Mohan, T. Yu, B. P. Sala, H. Hebaishi, A. Caruso, A. C. Marques, C. Michetti, M. E. Smachetti, A. Shah, M. Sabbioni, O. Kulhanci, W. W. Tee, D. Reinberg, M. L. Scattoni, H. Volk, I. McGonnell, F. C. Wardle, C. Fernandes and M. A. Basson, The chromatin remodeling factor CHD7 controls cerebellar development by regulating reelin expression, J Clin Invest, 127 (3), pp874-887, 2017. Pubmed

2017 C. Yzydorczyk, N. Li, H. Chehade, D. Mosig, M. Bidho, B. Keshavjee, J. B. Armengaud, K. Nardou, B. Siddeek, M. Benahmed, C. Vergely and U. Simeoni, Transient postnatal overfeeding causes liver stress-induced premature senescence in adult mice, Sci Rep, 7 (1), pp12911, 2017. Pubmed

2017 C. Yzydorczyk, J. B. Armengaud, A. C. Peyter, H. Chehade, F. Cachat, C. Juvet, B. Siddeek, S. Simoncini, F. Sabatier, F. Dignat-George, D. Mitanchez and U. Simeoni, Endothelial dysfunction in individuals born after fetal growth restriction: cardiovascular and renal consequences and preventive approaches, J Dev Orig Health Dis, pp1-17, 2017. Pubmed

2017 C. Xu, M. Lang-Muritano, F. Phan-Hug, A. A. Dwyer, G. P. Sykiotis, D. Cassatella, J. Acierno, Jr., M. Mohammadi and N. Pitteloud, Genetic testing facilitates prepubertal diagnosis of congenital hypogonadotropic hypogonadism, Clin Genet, 2017. Pubmed

2017 C. Xu, D. Cassatella, A. M. van der Sloot, R. Quinton, M. Hauschild, C. De Geyter, C. Fluck, K. Feller, D. Bartholdi, A. Nemeth, I. Halperin, S. Pekic Djurdjevic, P. Maeder, G. Papadakis, A. A. Dwyer, L. Marino, L. Favre, D. Pignatelli, N. J. Niederlander, J. Acierno, Jr. and N. Pitteloud, Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants, Genet Med, 2017. Pubmed

2017 C. Xu, A. Messina, E. Somm, H. Miraoui, T. Kinnunen, J. Acierno, Jr., N. J. Niederlander, J. Bouilly, A. A. Dwyer, Y. Sidis, D. Cassatella, G. P. Sykiotis, R. Quinton, C. De Geyter, M. Dirlewanger, V. Schwitzgebel, T. R. Cole, A. A. Toogood, J. M. Kirk, L. Plummer, U. Albrecht, W. F. Crowley, Jr., M. Mohammadi, M. Tena-Sempere, V. Prevot and N. Pitteloud, KLB, encoding beta-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism, EMBO Mol Med, 9 (10), pp1379-1397, 2017. Pubmed

2017 C. Tran, J. Serratrice, J. M. Nuoffer, A. Schaller, B. Favrat, F. Barbey, J. A. Lobrinus, I. Kern, T. Kuntzer and D. Ballhausen, [Raising the internist’s know-how in the field of rare diseases: mitochondrial diseases as an illustrative example], Rev Med Suisse, 13 (546), pp159-163, 2017. Pubmed

2017 C. Sandi, O. Barrie, H. Kanu and F. Sesay, Notes from the Field: Impact of Increasing the Number of Ebola Surveillance Officers - Kambia District, Sierra Leone, September 2014-September 2015, MMWR Morb Mortal Wkly Rep, 66 (3), pp90-91, 2017. Pubmed