G Koch

242 Specificity of effects of the share to care training for physicians – a pre-post trial

Anja Schuldt-Joswig, Margarethe Gregersen, Claudia Hacke, Christina Gesine Sommer et autres

de, us, au (code pays fourni par la source)

288 Implementation and adaptation of the nurse module within the share to care program

Christine Wagner-Ullrich, Constanze Stolz-Klingenberg, Claudia Bünzen, Anja Schuldt-Joswig et autres

de (code pays fourni par la source)

Patient-reported effects of hospital-wide implementation of shared decision-making at a university medical centre in Germany: a pre–post trial

Fueloep Scheibler, Friedemann Geiger, Kai Wehkamp, Marion Danner et autres

de, us (code pays fourni par la source)

Global Alliance for the Promotion of Physical Activity: the Hamburg Declaration

Jürgen M. Steinacker, Willem van Mechelen, Wilhelm Bloch, Mats Börjesson et autres

de, ch, ie, Afrique du Sud, au, nl, se, it, ru, ae, ua, at, us, es, il, be, fr, ar, nz, jp, ro, pl, lv, gr, sg, ee, qa, lt, pt, ca (code pays fourni par la source)

Hematopoietic Stem Cell Transplantation in an Infant with Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome

Katharina L. Gössling, Cyrill Schipp, Ute Fischer, Florian Babor et autres

de (code pays fourni par la source)

Four New Cases of Congenital Secondary Hypothyroidism due to a Splice Site Mutation in the Thyrotropin-β Gene: Phenotypic Variability and Founder Effect

Guntram Borck, A. Kemal Topaloğlu, Eckhard Korsch, Ursula Martiné et autres

fr, de, tr, us (code pays fourni par la source)

Congenital Secondary Hypothyroidism Caused by Exon Skipping due to a Homozygous Donor Splice Site Mutation in the TSHβ-Subunit Gene

Joachim Pohlenz, Alexandra M. Dumitrescu, Ulrich Aumann, G Koch et autres

de, us (code pays fourni par la source)

Infantile Presentation of the mtDNA A3243G tRNALeu (UUR) Mutation

E. J. Okhuijsen-Kroes, J. M. F. Trijbels, R. C. A. Sengers, Edwin C.M. Mariman et autres

nl, de (code pays fourni par la source)

["Release in the destruction of worthless life" by Binding and Hoche from the viewpoint of German psychiatry before 1933].

G Koch

[Recessive microencephaly linked to the X chromosome].

Yves Deshaies, H.‐D. Rott, H F Wissmuller, Gesa Schwanitz et autres

[Contribution to information and genetic counseling in Mekkel's syndrome (author's transl)].

G Koch, Gesa Schwanitz

[Chromosomes and paternity. (New aspects of forensic human genetics)].

G Koch, Gesa Schwanitz