BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 27480187)

  • 1. [Healthcare services for people in Lower Saxony (Germany) suffering from a rare disease: Findings from a survey among medical professionals].
    Pauer F; Pflaum U; Lührs V; Frank M; Graf von der Schulenburg JM
    Z Evid Fortbild Qual Gesundhwes; 2016; 113():36-44. PubMed ID: 27480187
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Evaluation of a future scenario concerning the use of big data applications to improve the care of people with rare diseases].
    Sedlmayr B; Knapp A; Kümmel M; Bathelt F; Sedlmayr M
    Z Evid Fortbild Qual Gesundhwes; 2020 Dec; 158-159():81-91. PubMed ID: 33250393
    [TBL] [Abstract][Full Text] [Related]  

  • 3. State of knowledge about information sources and health care centres for rare diseases among affected people in Germany.
    Hanisch M; Wiemann S; Bohner L; Jung S; Kleinheinz J
    Cent Eur J Public Health; 2020 Mar; 28(1):82-84. PubMed ID: 32228824
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Measures to improve the health situation of patients with rare diseases in Germany. A comparison with the National Action Plan].
    Frank M; Eidt-Koch D; Aumann I; Reimann A; Wagner TO; Graf von der Schulenburg JM
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2014 Oct; 57(10):1216-23. PubMed ID: 25209683
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [European Reference Networks : Consequences for healthcare in Germany].
    Graessner H; Schäfer F; Scarpa M; Wagner TOF
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2017 May; 60(5):537-541. PubMed ID: 28275837
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [se-atlas - the health service information platform for people with rare diseases : Supporting research on medical care institutions and support groups].
    Haase J; Wagner TOF; Storf H
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2017 May; 60(5):503-509. PubMed ID: 28275836
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Interdisciplinary care path and potential IT support for people with rare diseases in Germany].
    Zoch M; Sedlmayr B; Knapp A; Bathelt F; Helfer S; Schmitt J; Sedlmayr M
    Z Evid Fortbild Qual Gesundhwes; 2021 Oct; 165():68-76. PubMed ID: 34483074
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Potentials and current shortcomings in the cooperation between German centers for rare diseases and primary care physicians: results from the project TRANSLATE-NAMSE.
    Druschke D; Krause F; Müller G; Scharfe J; Hoffmann GF; Schmitt J;
    Orphanet J Rare Dis; 2021 Nov; 16(1):494. PubMed ID: 34819135
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Japan as the front-runner of super-aged societies: Perspectives from medicine and medical care in Japan.
    Arai H; Ouchi Y; Toba K; Endo T; Shimokado K; Tsubota K; Matsuo S; Mori H; Yumura W; Yokode M; Rakugi H; Ohshima S
    Geriatr Gerontol Int; 2015 Jun; 15(6):673-87. PubMed ID: 25656311
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Patient experiences of interprofessional collaboration and intersectoral communication in rare disease healthcare in Germany - a mixed-methods study.
    Inhestern L; Otto R; Brandt M; Zybarth D; Oheim R; Schüler H; Mir TS; Tsiakas K; Dibaj P; Zschüntzsch J; Okun PM; Hegenbart U; Sommerburg O; Schramm C; Weiler-Normann C; Härter M; Bergelt C
    Orphanet J Rare Dis; 2024 May; 19(1):197. PubMed ID: 38741100
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Speak up for people with rare diseases: ACHSE : ACHSE, Rare Diseases Germany, and its network].
    Mundlos C
    Internist (Berl); 2018 Dec; 59(12):1327-1334. PubMed ID: 30377713
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Which strategies might improve local primary healthcare in Germany? An explorative study from a local government point of view.
    Kuhn B; Kleij KS; Liersch S; Steinhäuser J; Amelung V
    BMC Fam Pract; 2017 Dec; 18(1):105. PubMed ID: 29262798
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Hospitalization of Migrants without Health Insurance: An Explorative Study of Hospital Healthcare in Lower Saxony, Berlin and Hamburg].
    Mylius M
    Gesundheitswesen; 2016 Apr; 78(4):203-8. PubMed ID: 27078830
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Seven years of the National Action League for People with Rare Diseases : NAMSE - a success story?!].
    Halbach A; Schnieders B; Knufmann-Happe K
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2017 May; 60(5):479-486. PubMed ID: 28337510
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Hungarian national plan and strategy for rare diseases].
    Kosztolányi G
    Orv Hetil; 2014 Mar; 155(9):325-8. PubMed ID: 24566695
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Survey of healthcare experiences of Australian adults living with rare diseases.
    Molster C; Urwin D; Di Pietro L; Fookes M; Petrie D; van der Laan S; Dawkins H
    Orphanet J Rare Dis; 2016 Mar; 11():30. PubMed ID: 27012247
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Healthcare networks for people with rare diseases: integrating data and expertise].
    Graessner H; Storf H; Schaefer F
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2022 Nov; 65(11):1164-1169. PubMed ID: 36167994
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Access to information supporting availability of medicines for patients suffering from rare diseases looking for possible treatments: the EuOrphan Service.
    Stakisaitis D; Spokiene I; Juskevicius J; Valuckas KP; Baiardi P
    Medicina (Kaunas); 2007; 43(6):441-6. PubMed ID: 17637514
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Rare diseases, digitization, and the National Action League for People with Rare Diseases (NAMSE)].
    Wessel T; Heuing K; Schlangen M; Schnieders B; Algermissen M
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2022 Nov; 65(11):1119-1125. PubMed ID: 36239769
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Orphanet and its consortium: where to find expert-validated information on rare diseases].
    Maiella S; Rath A; Angin C; Mousson F; Kremp O
    Rev Neurol (Paris); 2013 Feb; 169 Suppl 1():S3-8. PubMed ID: 23452769
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.