Janika Blömeke
Janika Blömeke
M. Sc.
  • Wissenschaftliche Mitarbeiterin
Arbeitsbereich

Standort

W26 , 2. Etage
Sprachen
Deutsch (Muttersprache)

Tätigkeitsschwerpunkte

Publikationen

2019

Psychometric properties of the quality of life in short statured youth (QoLISSY) questionnaire within the course of growth hormone treatment
Bloemeke J, Silva N, Bullinger M, Witt S, Dörr H, Quitmann J
HEALTH QUAL LIFE OUT. 2019;17(1):49.

Quality of Life in Adolescent Boys with Idiopathic Short Stature: Positive Impact of Growth Hormone and Aromatase Inhibitors
Bullinger M, Bloemeke J, Mericq V, Sommer R, Gaete X, Ross J, Yu Y, Permuy J, Gagliardi P, Damaso Y, Mauras N
Horm Res Paediat. 2019 [Epub ahead of print];90(6):381-392.

Quality of Life of Short-Statured Children Born Small for Gestational Age or Idiopathic Growth Hormone Deficiency Within 1 Year of Growth Hormone Treatment
Quitmann J, Bloemeke J, Silva N, Bullinger M, Witt S, Akkurt I, Dunstheimer D, Vogel C, Böttcher V, Kuhnle Krahl U, Bettendorf M, Schönau E, Fricke-Otto S, Keller A, Mohnike K, Dörr H
FRONT PEDIATR. 2019;7:164.

Agreement between mothers', fathers', and children's' ratings on health-related quality of life in children born with esophageal atresia - a German cross-sectional study
Witt S, Bloemeke J, Bullinger M, Dingemann J, Dellenmark-Blom M, Quitmann J
BMC PEDIATR. 2019;19(1):330.

Quality of life of children with achondroplasia and their parents - a German cross-sectional study
Witt S, Kolb B, Bloemeke J, Mohnike K, Bullinger M, Quitmann J
ORPHANET J RARE DIS. 2019;14(1):194.

2018

The psychometric evaluation of the quality of life in short stature youth (QoLISSY) instrument for German children born small for gestational age
Sommer R, Blömeke J, Bullinger M, Quitmann J
J ENDOCRINOL INVEST. 2018;41(10):1185-1191.

Adrenogenitales Syndrom (AGS) mit 21-Hydroxylase-Defekt bei Kleinkindern: Erste Ergebnisse einer Pilotstudie zur psychosozialen Situation der Eltern
Witt S, Blömeke J, Dörr H, Quitmann J
Päd Praxis. 2018;90(1):29-37.

2017

An ICF-CY-based approach to assessing self- and observer-reported functioning in young persons with achondroplasia - development of the pilot version of the Achondroplasia Personal Life Experience Scale (APLES)
Sommer R, Blömeke J, Dabs M, Witt S, Bullinger M, Quitmann J
DISABIL REHABIL. 2017;39(24):2499-2503.

Letzte Aktualisierung aus dem FIS: 09.12.2019 - 00:36 Uhr