Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sandra Mehmecke"'
Autor:
Lorenz Grigull, Sandra Mehmecke, Ann-Katrin Rother, Susanne Blöß, Christian Klemann, Ulrike Schumacher, Urs Mücke, Xiaowei Kortum, Werner Lechner, Frank Klawonn
Publikováno v:
PLoS ONE, Vol 14, Iss 10, p e0222637 (2019)
BackgroundRare diseases (RD) result in a wide variety of clinical presentations, and this creates a significant diagnostic challenge for health care professionals. We hypothesized that there exist a set of consistent and shared phenomena among all in
Externí odkaz:
https://doaj.org/article/16d3e39f00444d9c9759dab9ad7f2fa0
Autor:
Susanne Blöß, Christian Klemann, Ann-Katrin Rother, Sandra Mehmecke, Ulrike Schumacher, Urs Mücke, Martin Mücke, Christiane Stieber, Frank Klawonn, Xiaowei Kortum, Werner Lechner, Lorenz Grigull
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0172532 (2017)
BACKGROUND:Worldwide approximately 7,000 rare diseases have been identified. Accordingly, 4 million individuals live with a rare disease in Germany. The mean time to diagnosis is about 6 years and patients receive several incorrect diagnoses during t
Externí odkaz:
https://doaj.org/article/f16cad86a168453bae12b99a4a61ed3c
Autor:
Sandra Mehmecke
Publikováno v:
kma - Klinik Management aktuell. 28:70-72
Mit dem Pflegepersonal-Stärkungsgesetz wurden die Personalkosten des Pflegedienstes aus den Fallpauschalen ausgegliedert. Was seitdem passiert ist, und wie es weitergehen könnte.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb7059a848f969ebd0fc8544b0dc1319
https://doi.org/10.1055/s-0043-1762880
https://doi.org/10.1055/s-0043-1762880
Autor:
Lorenz Grigull, Christina Lampe, Xiauwei Kortum, Nicole Muschol, Frank Klawonn, Werner Lechner, Susanne Blöß, Anibh M. Das, Anna-Lena Sieg, Sandra Mehmecke, Anja Köhn
Publikováno v:
Klinische Pädiatrie. 231:60-66
Zusammenfassung Hintergrund Die Diagnosestellung einer seltenen Stoffwechselerkrankung stellt eine Herausforderung für Familien und betreuende Ärzte dar. Um den Weg zur Diagnose zu unterstützen, wurde ein diagnostisches Werkzeug entwickelt, welche
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e9726c26cd3050c878adc81840a7de
https://doi.org/10.1055/a-0816-5681
https://doi.org/10.1055/a-0816-5681
Autor:
Xiaowei Kortum, Ann-Katrin Rother, Urs Mücke, Werner Lechner, Sandra Mehmecke, Lorenz Grigull, Frank Klawonn, Susanne Blöß, Christian Klemann, Ulrike Schumacher
Publikováno v:
e0222637
PLoS ONE
PLoS ONE, Vol 14, Iss 10, p e0222637 (2019)
PLoS ONE
PLoS ONE, Vol 14, Iss 10, p e0222637 (2019)
BackgroundRare diseases (RD) result in a wide variety of clinical presentations, and this creates a significant diagnostic challenge for health care professionals. We hypothesized that there exist a set of consistent and shared phenomena among all in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea5cddd25b59fc579b4b4283814404a9
https://hdl.handle.net/10033/621996
https://hdl.handle.net/10033/621996
Autor:
Lorenz Grigull, Sandra Mehmecke, Ann-Katrin Rother, Susanne Bloess, Christian Klemann, Ulrike Schumacher, Urs Mücke, Xiaowei Kortum, Werner Lechner, Frank Klawonn
BACKGROUND Different rare diseases (RD) obviously result in substantial clinical appearances and diagnostic challenges for health professionals. However, we hypothesized that there are consistencies and shared phenomena among all individuals affected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce03caf4345f16df804caa4405f5248b
https://doi.org/10.2196/preprints.11697
https://doi.org/10.2196/preprints.11697
Autor:
Ann-Katrin Rother, Martin Mücke, Urs Mücke, Lorenz Grigull, Frank Klawonn, Werner Lechner, Susanne Blöß, Christiane Stieber, Christian Klemann, Ulrike Schumacher, Sandra Mehmecke, Xiaowei Kortum
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0172532 (2017)
PLoS ONE
PLoS ONE
Background Worldwide approximately 7,000 rare diseases have been identified. Accordingly, 4 million individuals live with a rare disease in Germany. The mean time to diagnosis is about 6 years and patients receive several incorrect diagnoses during t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e797b7bfb037cde339c040a267451c1
http://europepmc.org/articles/PMC5325301?pdf=render
http://europepmc.org/articles/PMC5325301?pdf=render
Autor:
Sandra, Mehmecke, Carolin, Ohler, Manuel, Ahting, Ulrike, Schumacher, Mike, Ridder, Blanka, Schmidt, Annika, Hiber
Publikováno v:
Pflege Zeitschrift. 64(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::15110e9374adf40a2de87c7c0fbe520f
https://pubmed.ncbi.nlm.nih.gov/21462460
https://pubmed.ncbi.nlm.nih.gov/21462460
Autor:
Werner Lechner, Reinhard Dengler, Susanne Petri, Frank Klawonn, Xiaowei Kortum, Katja Kollewe, C. Köhler, Christiane Schneider-Gold, Anne-Katrin Güttsches, Thomas Lücke, Lorenz Grigull, Sandra Mehmecke, Ulrike Schumacher
Publikováno v:
BMC Medical Informatics and Decision Making
Background Diagnosis of neuromuscular diseases in primary care is often challenging. Rare diseases such as Pompe disease are easily overlooked by the general practitioner. We therefore aimed to develop a diagnostic support tool using patient-oriented
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fe251f97176594d3590544dc0329925