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Einrichtungen, die nicht zum Universitätsklinikum Erlangen gehören
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
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Publications
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Research Grants
(200)
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Formation of the node of Ranvier by Schwann cells is under control of transcription factor Sox10 (2021)
Saur AL, Fröb F, Weider M, Wegner M
Journal article
Optimal trees selection for classification via out-of-bag assessment and sub-bagging (2021)
Khan Z, Gul N, Faiz N, Gul A, Adler W, Lausen B
Journal article
Gradient boosting for linear mixed models (2021)
Griesbach C, Säfken B, Waldmann E
Journal article
Prototypical clinical trial registry based on fast healthcare interoperability resources (FHIR): Design and implementation study (2021)
Gulden C, Blasini R, Nassirian A, Stein A, Altun FB, Kirchner M, Prokosch HU, Boeker M
Journal article
A clinical trial: Aqualizer ™ therapy and its effects on myopathies or temporomandibular dysfunctions. Part II: Subjective parameters (2021)
Buchbender M, Keplinger L, Kesting MR, Adler W, Schmitt C
Journal article
Human papilloma virus genotype distribution in women with premalignant or malignant lesions of the uterine cervix (2021)
Stübs F, Gaß P, Dietl A, Schulmeyer C, Adler W, Geppert CI, Hartmann A, et al.
Journal article
Human wrist anatomy: anatomical features important for treatment of palmar dislocation of the lunate bone (2021)
Wozniak S, Szpotowicz G, Bienias M, Kedzierski B, Sosnowska D, Szymocha M, Wasilewska E, et al.
Conference contribution
New anatomy-related ratios describing the risk of incomplete colonoscopy in human patients (2021)
Wozniak S, Kempinski R, Pytrus T, Zazga M, Szymocha M, Domagala Z, Davies DC, Paulsen F
Conference contribution
Diameters of umbilical and portal veins and ductus venosus in the human foetuses after 20 weeks of gestation in an ultrasound examination (2021)
Wozniak S, Florjanski J, Piatek A, Tomialowicz M, Zazga M, Szymocha M, Domagala Z, et al.
Conference contribution
Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP sydrome) caused by a novel mutation in ADPRHL2 (AHR3) (2021)
Durmus H, Mertoğlu E, Sticht H, Ceylaner S, Kulaksızoğlu IB, Hashemolhosseini S, Uçar EÖ, Parman Y
Journal article
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