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Department of Paediatrics and Adolescent Medicine
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Overview
Publications
(1,220)
Research Grants
(33)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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Authored book
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Thesis
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Liquid Biopsies in Ewing Sarcoma (2021)
Krumbholz M, Metzler M
Book chapter / Article in edited volumes
MAP2K1-MUTATED ECD/RDD-OVERLAP NON-LANGERHANS CELL HISTIOCYTOSIS RESPONDING TO COBIMETINIB (2021)
Classen CF, Leyh J, Rümmele P, Rosenwald A, Metzler M
Conference contribution
Methods for the Administration of EDAR Pathway Modulators in Mice (2021)
Schuepbach-Mallepell S, Kowalczyk-Quintas C, Dick A, Eslami M, Vigolo M, Headon DJ, Cheeseman M, et al.
Book chapter / Article in edited volumes
Safety of clonidine used for long-term sedation in paediatric intensive care: A systematic review (2020)
Eberl S, Ahne G, Toni I, Standing J, Neubert A
Journal article, Review article
The Development of Integrin Alpha-8 Deficient Lungs Shows Reduced and Altered Branching and a Correction of the Phenotype During Alveolarization (2020)
Cremona TP, Hartner A, Schittny JC
Journal article
Expanding the spectrum of WDR62 mutations : description of new cases (2020)
Ruaud L, Drunat S, Ernault A, Capri Y, Van Maldergem L, Engel C, Altuzarra C, et al.
Conference contribution
Incidence of Secondary Malignancies After TBI/VP16 Conditioning for Childhood All - Results of the Prospective ALL-SCT-BFM-2003 Trial (2020)
Eichinger A, Glogova E, Beier R, Guengoer T, Stachel D, Stachel D, Lang P, et al.
Conference contribution
Germline variants in transcription factor HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms (2020)
Van Walree ES, Dombrowsky G, Jansen IE, Mirkov MU, Zwart R, Ilgun A, Guo D, et al.
Conference contribution
Tetrasomy of SCN2A associated with refractory neonatal epileptic encephalopathy (2020)
Krumbiegel M, Trollmann R, Mammadova D, Schnell A, Kraus C, Ekici AB, Reis A, Zweier C
Conference contribution
Unexpected phenotypic variability in a family with epilepsy explained by independent segregation of biparental CACNA1A loss-of-function variants (2020)
Kraus C, Mammadova D, Leis T, Ekici AB, Thiel C, Reis A, Trollmann R
Conference contribution
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