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Klinik und Poliklinik für Kinder- und Jugendmedizin

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Lampe, Christina; Hendriksz, Christian J.; Lavery, Christine et al.

Burden of disease suffered by caregivers of patients with Morquio syndrome type A: results from a self-reported outcomes survey

MOLECULAR GENETICS AND METABOLISM. Bd. 111. H. 2. 2014 S. S65-S65


Hendriksz, Christian J.; Lavery, Christine; Lampe, Christina et al.

Burden of disease suffered by patients with Morquio syndrome type A: results from a patient-reported outcomes survey

MOLECULAR GENETICS AND METABOLISM. Bd. 111. H. 2. 2014 S. S53-S54


Eggermann, Thomas; Binder, Gerhard; Brioude, Frederic et al.

CDKN1C mutations: two sides of the same coin

TRENDS IN MOLECULAR MEDICINE. Bd. 20. H. 11. 2014 S. 614-622


Benesch, Martin; Warmuth-Metz, Monika; von Bueren, Andre O. et al.

CENTRALLY REVIEWED GLIOMATOSIS CEREBRI IN CHILDREN AND ADOLESCENTS: A RETROSPECITVE ANALYSIS FROM THE HIT-HGG DATABASE

NEURO-ONCOLOGY. Bd. 16. 2014 S. 42-42


Beck, Michael; Moreels, Marjan; Quintens, Roel et al.

Chronic exposure to simulated space conditions predominantly affects cytoskeleton remodeling and oxidative stress response in mouse fetal fibroblasts

INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE. Bd. 34. H. 2. 2014 S. 606-615



Eggermann, Thomas; Algar, Elizabeth; Lapunzina, Pablo et al.

Clinical utility gene card for: Beckwith-Wiedemann Syndrome

EUROPEAN JOURNAL OF HUMAN GENETICS. Bd. 22. H. 3. 2014


Huenseler, Christoph; Balling, Gunter; Roehlig, Christoph et al.

Continuous Infusion of Clonidine in Ventilated Newborns and Infants: A Randomized Controlled Trial

PEDIATRIC CRITICAL CARE MEDICINE. Bd. 15. H. 6. 2014 S. 511-522


Rueegger, Corinne M.; Lindner, Martin; Ballhausen, Diana et al.

Cross-sectional observational study of 208 patients with non-classical urea cycle disorders

JOURNAL OF INHERITED METABOLIC DISEASE. Bd. 37. H. 1. 2014 S. 21-30


Karabul, Nesrin; Arash, Laila; Kircher, Martina et al.

Cytokine profiles in Fabry patients

MOLECULAR GENETICS AND METABOLISM. Bd. 111. H. 2. 2014 S. S59-S59