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Klinik und Poliklinik für Kinder- und Jugendmedizin

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Ripperger, Tim; Bielack, Stefan S.; Borkhardt, Arndt et al.

Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. Bd. 173. H. 4. 2017 S. 1017-1037


Giugliani, Roberto; Scarpa, Maurizio; Tylki-Szymanska, Anna et al.

Clinical outcomes after 3 years of idursulfase treatment in patients with MPS II: data from the Hunter Outcome Survey (HOS)

MOLECULAR GENETICS AND METABOLISM. Bd. 120. H. 1-2. 2017 S. S56-S56


Hughes, D.; Giugliani, R.; Guffon, N. et al.

Clinical outcomes in a subpopulation of adults with Morquio A syndrome: results from a long-term extension study of elosulfase alfa

ORPHANET JOURNAL OF RARE DISEASES. Bd. 12. 2017


Muenzer, Joseph; Giugliani, Roberto; Scarpa, Maurizio et al.

Clinical outcomes in idursulfase-treated patients with mucopolysaccharidosis type II: 3-year data from the hunter outcome survey (HOS)

ORPHANET JOURNAL OF RARE DISEASES. Bd. 12. 2017


Gal, Andreas; Beck, Michael; Hoeppner, Wolfgang et al.

Clinical utility gene card for: Fabry disease - update 2016

EUROPEAN JOURNAL OF HUMAN GENETICS. Bd. 25. H. 7. 2017 S. E1-E3


McGovern, Margaret M.; Dionisi-Vici, Carlo; Giugliani, Roberto et al.

Consensus recommendation for a diagnostic guideline for acid sphingomyelinase deficiency

GENETICS IN MEDICINE. Bd. 19. H. 9. 2017 S. 967-974


Wasserstein, Melissa; Dionisi-Vici, Carlo; Giugliani, Roberto et al.

Consensus recommendation on a diagnostic guideline for acid sphingomyelinase deficiency

MOLECULAR GENETICS AND METABOLISM. Bd. 120. H. 1-2. 2017 S. S138-S138


Kowalzik, F.; Faber, J.; Knuf, M.

Correlates for Infection Protection after Vaccination

MONATSSCHRIFT KINDERHEILKUNDE. Bd. 165. H. 7. 2017 S. 588-595


Niehues, T.; Zepp, F.

Current Principles of the Diagnosis of Immunodeficiency Diseases

MONATSSCHRIFT KINDERHEILKUNDE. Bd. 165. H. 12. 2017 S. 1060-1062


Hennermann, J. B.

Development of new therapies for rare diseases. Example: lysosomal storage disorders

MONATSSCHRIFT KINDERHEILKUNDE. Bd. 165. H. 3. 2017 S. 226-232