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Canet J et al PERISCOPE Investigators, C J; Laufenberg-Feldmann, Rita, R.L.; Malte Brunier, M.B. et al.

Development and validation of a score to predict postoperative respiratory failure in a multicentre European cohort: A prospective, observational study.

EUR J Anesthesiol. Bd. 32. 2015 S. 458-470


Melo, Esther; Kasper, Jennifer Y.; Unger, Ronald E. et al.

Development of a Bronchial Wall Model: Triple Culture on a Decellularized Porcine Trachea

TISSUE ENGINEERING PART C-METHODS. Bd. 21. H. 9. 2015 S. 909-921


Eckart, K.; Roehrich, J.; Breitmeier, D. et al.

Development of a new multi-analyte assay for the simultaneous detection of opioids in serum and other body fluids using liquid chromatography-tandem mass spectrometry

JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES. Bd. 1001. 2015 S. 1-8


Richter, F.; Strauss, B.; Braehler, E. et al.

Development of a Short Version of the Eating Attitudes Tests (EAT) and Prevalence of abnormal Eating Behavior in the german Population

ZEITSCHRIFT FUR PSYCHOSOMATISCHE MEDIZIN UND PSYCHOTHERAPIE. Bd. 61. H. 1. 2015 S. 93-93



Zolfaghari, Shabnam; Harenberg, Job; Froelich, Lutz et al.

Development of Recommendations to Continue Anticoagulation with One of the Two Types of Oral Anticoagulants Based on the Identification of Patients' Preference

SEMINARS IN THROMBOSIS AND HEMOSTASIS. Bd. 41. H. 2. 2015 S. 166-177


Wagner, Stefanie; Maurer, Jana; Pape, Valeska et al.

Development of Three Alternate Forms for the Assessment of Alternating Phonemic and Semantic Verbal Fluency

ZEITSCHRIFT FUR NEUROPSYCHOLOGIE. Bd. 26. H. 1. 2015 S. 27-34


Vona, B.; Hofrichter, M. A. H.; Neuner, C. et al.

DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics

CLINICAL GENETICS. Bd. 87. H. 1. 2015 S. 49-55


Vona, B.; Hofrichter, M. A. H.; Neuner, C. et al.

DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics

CLINICAL GENETICS. Bd. 87. H. 1. 2015 S. 49-55


Ehlers, V; Willershausen, B

Diagnose und Therapieansätze der frühkindlichen Karies

KZV aktuell. Bd. 1. 2015 S. 20-23