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Klinik und Poliklinik für Kinder- und Jugendmedizin

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Hughes, DA; Al-Sayed, M; Belmatoug, N et al.

Early access experience with VPRIV (R): Recommendations for 'core data' collection

BLOOD CELLS MOLECULES AND DISEASES. Bd. 47. H. 2. 2011 S. 140-142


Schulze-Frenking, G; Jones, SA; Roberts, J et al.

Effects of enzyme replacement therapy on growth in patients with mucopolysaccharidosis type II

JOURNAL OF INHERITED METABOLIC DISEASE. Bd. 34. H. 1. 2011 S. 203-208


Lindner, Martin; Gramer, Gwendolyn; Haege, Gisela et al.

Efficacy and outcome of expanded newborn screening for metabolic diseases - report of 10 years from south-west Germany

Orphanet journal of rare diseases. Bd. 6. London: Biomed Central 2011 S. 44



El-Gharbawy, AH; Bhat, G; Murillo, JE et al.

Expanding the clinical spectrum of late-onset Pompe disease: Dilated arteriopathy involving the thoracic aorta, a novel vascular phenotype uncovered

MOLECULAR GENETICS AND METABOLISM. Bd. 103. H. 4. 2011 S. 362-366



Gramer, G; Lindner, M; Haege, G et al.

Extended newborn screening for metabolic diseases in South-West Germany-evaluation of efficacy and outcome

EUROPEAN JOURNAL OF PEDIATRICS. Bd. 170. H. 2. 2011 S. 264-264


Davies, EH; Mengel, E; Tylki-Szymanska, A et al.

Four-year follow-up of chronic neuronopathic Gaucher disease in Europeans using a modified severity scoring tool

JOURNAL OF INHERITED METABOLIC DISEASE. Bd. 34. H. 5. 2011 S. 1053-1059


Belmatoug, N; Burlina, A; Giraldo, P et al.

Gastrointestinal disturbances and their management in miglustat-treated patients

JOURNAL OF INHERITED METABOLIC DISEASE. Bd. 34. H. 5. 2011 S. 991-1001


Herzog, A; Hartung, R; Mengel, E et al.

Genotype-Phenotype Correlations in Pompe Disease

CLINICAL THERAPEUTICS. Bd. 33. 2011 S. S39-S39