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Zentrum für Kinder- und Jugendmedizin

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Gucev, Zoran; Tasic, Velibor; Bogevska, Ivona et al.

Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutation

EUROPEAN JOURNAL OF MEDICAL GENETICS. Bd. 63. H. 1. 2020


Lachmann, Anja; Kurschat, Christine; Fritsch, Almut et al.

Home infusion therapy with agalsidase alfa for patients with Fabry disease in Germany and Austria

MOLECULAR GENETICS AND METABOLISM. Bd. 129. H. 2. 2020 S. S94-S94


Mengel, Eugen; Stulnig, Thomas M.; Kralewski, Martina et al.

Home infusion therapy with velaglucerase alfa for Gaucher disease type 1 in Germany and Austria

MOLECULAR GENETICS AND METABOLISM. Bd. 129. H. 2. 2020 S. S109-S109


Choukair, Daniela; Eberle, Birgit; Vick, Philipp et al.

Identification ofTransient Receptor Potential Channel 4-Associated Proteinas a Novel Candidate Gene Causing Congenital Primary Hypothyroidism

HORMONE RESEARCH IN PAEDIATRICS. Bd. 93. H. 1. 2020 S. 16-29





Schwarz, Christoph E.; Kidszun, Andre; Bieder, Nicole S. et al.

Is faster better? A randomised crossover study comparing algorithms for closed-loop automatic oxygen control

ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION. Bd. 105. H. 4. 2020 S. F369-F374


Beetz, R.

Is there still no alternative to long-term antibacterial prophylaxis?

UROLOGE. Bd. 59. H. 3. 2020 S. 255-260


Westeppe, Sarah; Dionysopoulou, Anna; Kidszun, Andre et al.

Kagami-Ogata Syndrome: An Anomaly of the Ribs as a Pathognomonic Feature for the Clinical Diagnosis of an (epi)Genetic Syndrome

ZEITSCHRIFT FUR GEBURTSHILFE UND NEONATOLOGIE. Bd. 224. H. 3. 2020 S. 153-159