Lehrstuhl für Kinder- und Jugendmedizin


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
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Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

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Abstract

Journal

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