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Professur für Kinderheilkunde/Experimentelle Perinatalmedizin
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Department of Paediatrics and Adolescent Medicine
Lehrstuhl für Kinder- und Jugendmedizin
Overview
Publications
(92)
Research Grants
(7)
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Journal article
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Automatic recognition of the XLHED phenotype from facial images (2017)
Hadj-Rabia S, Schneider H, Navarro E, Klein O, Kirby N, Huttner K, Wolf L, et al.
Journal article
Hypohidrotic Ectodermal Dysplasia: Breastfeeding Complications Due to Impaired Breast Development (2017)
Wahlbuhl-Becker M, Faschingbauer F, Beckmann M, Schneider H
Journal article
ENGRAFTMENT, DIFFERENTIATION AND BIOLOGICAL EFFECTS OF CORD BLOOD-DERIVED CLONAL CELLS ADMINISTERED INTRAVENOUSLY TO NEWBORN RATS WITH HYPOXIC-ISCHEMIC BRAIN INJURY (2016)
Yang X, Griesmaier E, Wegleiter K, Schlager GW, Weisbach VG, Keller M, Park J, Schneider H
Conference contribution
Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements (2016)
Wohlfart S, Hammersen J, Schneider H
Journal article
Reduced Perinatal Leptin Availability May Contribute to Adverse Metabolic Programming in a Rat Model of Uteroplacental Insufficiency (2016)
Nuesken E, Wohlfarth M, Lippach G, Rauh M, Schneider H, Doetsch J, Nuesken KD
Journal article
Increased Rat Placental Fatty Acid, but Decreased Amino Acid and Glucose Transporters Potentially Modify Intrauterine Programming (2016)
Nuesken E, Gellhaus A, Kuehnel E, Swoboda I, Wohlfarth M, Vohlen C, Schneider H, et al.
Journal article
Electric Field-Induced Osteogenic Differentiation on TiO2 Nanotubular Layer (2016)
Park JH, Mazare AV, Schneider H, Mark K, Fischer M, Schmuki P
Journal article
Genotype, Clinical Course, and Therapeutic Decision Making in 76 Infants with Severe Generalized Junctional Epidermolysis Bullosa (2016)
Hammersen J, Has C, Naumann-Bartsch N, Stachel D, Kiritsi D, Söder S, Tardieu M, et al.
Journal article
A novel missense mutation in the gene EDARADD associated with an unusual phenotype of hypohidrotic ectodermal dysplasia (2016)
Wohlfart S, Söder S, Smahi A, Schneider H
Journal article
Strong hypoxia reduces leptin synthesis in purified primary human trophoblasts (2015)
Nuesken E, Herrmann Y, Wohlfarth M, Goecke TW, Appel S, Schneider H, Doetsch J, Nuesken KD
Journal article
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