Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Katrin Rother"'
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:
Ann-Katrin Rother, Nicolaus Schwerk, Folke Brinkmann, Frank Klawonn, Werner Lechner, Lorenz Grigull
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0135180 (2015)
Clinical symptoms in children with pulmonary diseases are frequently non-specific. Rare diseases such as primary ciliary dyskinesia (PCD), cystic fibrosis (CF) or protracted bacterial bronchitis (PBB) can be easily missed at the general practitioner
Externí odkaz:
https://doaj.org/article/6cf5e3c4737246c8ba428aead190fbbb
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
Publikováno v:
Journal of Osteopathic Medicine. 115:416-425
Context: Persistent low back pain (LBP) is a common complaint among women during and after pregnancy, and its effects on quality of life can be disabling. Objective: To evaluate the effectiveness of osteopathic manipulative therapy (OMTh; manipulativ
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