Starten Sie Ihre Suche...


Wir weisen darauf hin, dass wir technisch notwendige Cookies verwenden. Weitere Informationen

Klinik und Poliklinik für Kinder- und Jugendmedizin

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Tenenbaum-Rakover, Y; Mamanasiri, S; Ris-Stalpers, C et al.

Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis.

Clin Endocrinol (Oxf). Bd. 66. H. 5. 2007 S. 695-702


Boor, R; Jacobs, J; Hinzmann, A et al.

Combined spike-related functional MRI and multiple source analysis in the non-invasive spike localization of benign rolandic epilepsy

Clin Neurophysiol. Bd. 118. H. 4. 2007 S. 901-9



Prawitt, D

Das menschliche Genom

Lehrbuch Lentze-Schaub-Schulte-Spranger, Pädiatrie-Grundlagen und Praxis. 3. Aufl. Springer Medizin Verlag 2007



Lukacs, Z; Hartung, R; Beck, M et al.

Direct comparison of enzyme measurements from dried blood and leukocytes from male and female Fabry disease patients

J Inherit Metab Dis. Bd. 30. H. 4. 2007 S. 614


Wessler, I; Bittinger, F; Kamin, W et al.

Dysfunction of the non-neuronal cholinergic system in the airways and blood cells of patients with cystic fibrosis.

Life Sci. Bd. 80. H. 24-25. 2007 S. 2253-8


Ullmann, AJ; Krammes, E; Sommer, S et al.

Efficacy of posaconazole and amphotericin B in experimental invasive pulmonary aspergillosis in dexamethasone immunosuppressed rats.

J Antimicrob Chemother. Bd. 60. H. 5. 2007 S. 1080-4


Ries, M; Clarke, JT; Whybra, C et al.

Enzyme replacement in Fabry disease: pharmacokinetics and pharmacodynamics of agalsidase alpha in children and adolescents.

J Clin Pharmacol. Bd. 47. H. 10. 2007 S. 1222-30