957 resultados para Recherche de chemins
Resumo:
Osteogenesis imperfecta (OI) is a rare genetic disease. Today we are able to propose an adapted and efficient management to the patients with this rare disorder (and their families) thanks to a strong collaboration of clinicians and researchers. Recent knowledge regarding the genetics of OI permits an accurate diagnosis of the specific type of OI and its own molecular mechanism, a genetic counseling for family planning and prenatal diagnosis, and in addition more targeted therapeutic options. A specific support with re-education for patients with OI is necessary and efficient. To optimize patient care, a multidisciplinary consultation is proposed at the CHUV, moreover a web site is available for patients, families and therapists: www.infomaladiesrares.ch
Resumo:
1 kartta kahdellatoista lehdellä :, käsinvär. ;, n. 136 x 158 cm, lehdet n. 34 x 52,5 cm
Resumo:
1915/09/12 (N26)-1915/09/19.
Resumo:
1915/03/14 (N4).
Resumo:
1916/03/26 (N40)-1916/04/02.
Resumo:
1917/01/28 (N62)-1917/02/04.
Resumo:
1916/05/21 (N44)-1916/05/28.
Resumo:
Variante(s) de titre : La Recherche des disparus : organe officiel de l'Association française pour la recherche des disparus et de l'Agence des prisonniers de guerre de la Croix-rouge française
Resumo:
1916/02/27 (N38)-1916/03/05.
Resumo:
1915/06/13 (N18).
Resumo:
1915/04/22 (N9).
Resumo:
1916/10/22 (N55)-1916/10/29.
Resumo:
1916/01/16 (N35)-1916/01/23.