960 resultados para Recherche infirmière
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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
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1915/09/12 (N26)-1915/09/19.
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1915/03/14 (N4).
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1916/03/26 (N40)-1916/04/02.
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1917/01/28 (N62)-1917/02/04.
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1916/05/21 (N44)-1916/05/28.
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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
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1916/02/27 (N38)-1916/03/05.
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1915/06/13 (N18).
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1915/04/22 (N9).
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1916/10/22 (N55)-1916/10/29.
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1916/01/16 (N35)-1916/01/23.
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1915/05/16 (N14).
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1916/07/30 (N49)-1916/08/06.
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1916/08/27 (N51)-1916/09/03.
