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Lehrstuhl für Kinder- und Jugendmedizin
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Department of Paediatrics and Adolescent Medicine
Overview
Publications
(621)
Research Grants
(15)
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Journal article
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Fatigue and depression predict health-related quality of life in patients with pediatric-onset multiple sclerosis (2019)
Gravesande KSV, Blaschek A, Calabrese P, Rostasy K, Huppke P, Kessler JJ, Kalbe E, et al.
Journal article
Comparative Socioeconomic Study Of Patients In Germany With Dravet Syndrome, Refractory Epilepsy Or Epilepsy In Seizure Remission, And Their Caregivers (2019)
Strzelczyk A, Schubert-Bast S, Bast T, Bettendorf U, Hamer H, Herting A, Kalski M, et al.
Conference contribution
A novel mutation of the StAR gene with congenital adrenal hyperplasia and its association with heterochromia iridis: a case report (2019)
Splittstösser V, Schreiner F, Gohlke B, Welzel M, Holterhus PM, Wölfle J
Journal article
Prenatal diagnosis of HNF1B-associated renal cysts: Is there a need to differentiate intragenic variants from 17q12 microdeletion syndrome? (2019)
Vasileiou G, Hoyer J, Thiel C, Schaefer JT, Zapke M, Krumbiegel M, Kraus C, et al.
Journal article
The preleukemic TCF3-PBX1 gene fusion can be generated in utero and is present in ≈0.6% of healthy newborns (2019)
Hein D, Dreisig K, Metzler M, Izraeli S, Schmiegelow K, Borkhardt A, Fischer U
Journal article
Delineation of the clinical phenotype caused by de novo CLTC variants (2019)
Sa MJN, Venselaar H, Wiel L, Trimouille A, Lasseaux E, Naudion S, Lacombe D, et al.
Conference contribution
Clinical characteristics, resource utilization, quality of life and care situation for patients with Dravet syndrome in Germany (2019)
Kalski M, Schubert-Bast S, Kieslich M, Leyer AC, Polster T, Herting A, Mayer T, et al.
Journal article
Development and Usability Analysis of a Multimedia eConsent Solution (2019)
Schneiderheinze H, Prokosch HU, Apel H, Bellut L, Wullich B, Trollmann R, Schüttler C
Book chapter / Article in edited volumes
Homozygous Biallelic KRT5 Mutations in Epidermolysis Bullosa Simplex, Including a Complete Human Keratin 5 "Knock-Out", in Families with Extensive Consanguinity (2019)
Vahidnezhad H, Youssefian L, Daneshpazhooh M, Mahmoudi H, Kariminejad A, Fischer J, Christiansen J, et al.
Conference contribution
First-year predictors of health-related quality of life changes in short-statured children treated with human growth hormone (2019)
Quitmann J, Bloemeke J, Dörr HG, Bullinger M, Witt S, Silva N
Journal article
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