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Klinik und Poliklinik für Kinder- und Jugendmedizin

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Montano, Adriana M.; Lock-Hock, Ngu; Steiner, Robert D. et al.

Clinical course of sly syndrome (mucopolysaccharidosis type VII)

JOURNAL OF MEDICAL GENETICS. Bd. 53. H. 6. 2016 S. 403-418


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

Clinical outcomes in idursulfase-treated patients with MPS II: 3-year data from the Hunter Outcome Survey (HOS)

MOLECULAR GENETICS AND METABOLISM. Bd. 117. H. 2. 2016 S. S51-S51


Huemer, Martina; Mulder-Bleile, Regina; Burda, Patricie et al.

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency

JOURNAL OF INHERITED METABOLIC DISEASE. Bd. 39. H. 1. 2016 S. 115-124


Paret, Claudia; Theruvath, Johanna; Russo, Alexandra et al.

CNS HGNET-BCOR - MOLECULAR CHARACTERIZATION AND IDENTIFICATION OF POSSIBLE THERAPEUTIC TARGETS OF A NEW BRAIN TUMOR ENTITY

NEURO-ONCOLOGY. Bd. 18. 2016 S. 14-14


Zepp, F.

Communication in Hospitals and Practices

MONATSSCHRIFT KINDERHEILKUNDE. Bd. 164. H. 7. 2016 S. 556-557


Mueller, Thomas; Rasool, Insha; Heinz-Erian, Peter et al.

Congenital secretory diarrhoea caused by activating germline mutations in GUCY2C

GUT. Bd. 65. H. 8. 2016 S. 1306-1313


Schepp, Johanna; Bulashevska, Alla; Mannhardt-Laakmann, Wilma et al.

Deficiency of Adenosine Deaminase 2 Causes Antibody Deficiency

JOURNAL OF CLINICAL IMMUNOLOGY. Bd. 36. H. 3. 2016 S. 179-186


Hansen, G.; Kerbl, R.; Zepp, F.

Discussion on the Care of Neonates

MONATSSCHRIFT KINDERHEILKUNDE. Bd. 164. H. 12. 2016 S. 1124-1124


Kowalzik, Frank; Zepp, Fred; Hoffmann, Isabell et al.

Disease Burden of Rotavirus Gastroenteritis in Children Residing in Germany A Retrospective, Hospital-based Surveillance

PEDIATRIC INFECTIOUS DISEASE JOURNAL. Bd. 35. H. 1. 2016 S. 97-103


Kampmann, Christoph; Perrin, Amandine; Beck, Michael

Effectiveness of agalsidase alfa enzyme replacement in Fabry disease: cardiac outcomes after 10 years' treatment (vol 10, 125, 2015)

ORPHANET JOURNAL OF RARE DISEASES. Bd. 11. 2016