Exploring the genetic causes of isolated short stature. What has happened to idiopathic short stature? von Willems, M., Amouroux, C., Barat-Houari, M., Salles, J.-P., Edouard, T.

Volltext

Impairment of adipose tissue in Prader–Willi syndrome rescued by growth hormone treatment von Cadoudal, T, Buléon, M, Sengenès, C, Diene, G, Desneulin, F, Molinas, C, Eddiry, S, Conte-Auriol, F, Daviaud, D, Martin, P G P, Bouloumié, A, Salles, J-P, Tauber, M, Valet, P

Volltext

A crosstalk between the Wnt and the adhesion-dependent signaling pathways governs the chemosensitivity of acute myeloid leukemia von DE TONI, F, RACAUD-SULTAN, C, MANENTI, S, YSEBAERT, L, CHICANNE, G, MANSAT-DE MAS, V, CARIVEN, C, MESANGE, F, SALLES, J.-P, DEMUR, C, ALLOUCHE, M, PAYRASTRE, B

Volltext

Progressive Osseous Heteroplasia: A Model for the Imprinting Effects of GNAS Inactivating Mutations in Humans von Lebrun, M., Richard, N., Abeguilé, G., David, A., Dieux, A. Coëslier, Journel, H., Lacombe, D., Pinto, G., Odent, S., Salles, J. P., Taieb, A., Gandon-Laloum, S., Kottler, M. L.

Volltext

Hypophosphatasia: the contribution of imaging von Linglart, A., Salles, J.-P.

Volltext

Molecular markers of cartilage breakdown and synovitis at baseline as predictors of structural progression of hip osteoarthritis. The ECHODIAH Cohort von Mazières, B, Garnero, P, Guéguen, A, Abbal, M, Berdah, L, Lequesne, M, Nguyen, M, Salles, J-P, Vignon, E, Dougados, M

Volltext

Neuromuscular features of hypophosphatasia von Fonta, C., Salles, J.-P.

Volltext

Devenir de l'os de l'enfant né avec un retard de croissance intra-utérin von Salles, J.-P.

Volltext

Laboratory diagnosis of hypophosphatasia von Gennero, I., Conte-Auriol, F., Salles, J.-P.

Volltext

Hypophosphatasia: better knowledge for better care von Salles, J.-P., Linglart, A.

Volltext

Génétique des hypophosphatémies von Salles, J.-P.

Volltext

Biothérapie de l’hypophosphatasie von Salles, J.-P.

Volltext

Pathologies génétiques du FGF23 von Linglart, A., Salles, J.-P.

Volltext

Facteurs de l’ostéogenèse chez l’enfant von Salles, J.-P., Gennero, I., Moulin, P., Conte-Auriol, F., Edouard, T., Tauber, M.

Volltext

Physiopathologies des calcifications von Salles, J.-P.

Volltext

Approches translationnelles chez l’enfant von Salles, J.-P., Edouard, T., Gouze, J.-N., Conte-Auriol, F., Molinas-Casals, C., Raynal, P., Yart, A., Tauber, M., Gouze, E.

Volltext

How do Shp2 mutations that oppositely influence its biochemical activity result in syndromes with overlapping symptoms von Edouard, T, Montagner, A, Dance, M, Conte, F, Yart, A, Parfait, B, Tauber, M, Salles, J. P, Raynal, P

Volltext

Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paper von Bacchetta, J., Edouard, T., Laverny, G., Bernardor, J., Bertholet-Thomas, A., Castanet, M., Garnier, C., Gennero, I., Harambat, J., Lapillonne, A., Molin, A., Naud, C., Salles, J.P., Laborie, S., Tounian, P., Linglart, A.

Volltext

Prevalence of IGF1 deficiency in prepubertal children with isolated short stature von Edouard, T, Grünenwald, S, Gennero, I, Salles, J P, Tauber, M

Volltext

1,4-Naphthoquinones potently inhibiting P2X7 receptor activity von Faria, R.X., Oliveira, F.H., Salles, J.P., Oliveira, A.S., von Ranke, N.L., Bello, M.L., Rodrigues, C.R., Castro, H.C., Louvis, A.R., Martins, D.L., Ferreira, V.F.

Volltext