FB 04 - Universitätsmedizin
Johannes Gutenberg-Universität Mainz
- 06131/17-9704 oder 9799 (Sekretariat)
- 06131/17-9669
Miltner, O; Siebert, C; Tschaepe, R et al.
Muscular Trunk Stability in Professional and Amateur Volleyball PlayersZEITSCHRIFT FUR ORTHOPADIE UND UNFALLCHIRURGIE. Bd. 148. H. 2. 2010 S. 204-209
Knuf, M
Musik von Mozart führt zur Absenkung des Ruheenergieumsatzes bei FrühgeborenenKINDERÄRZTLICHE PRAXIS. Bd. 81. H. 2. 2010 S. 70
Bros, M; Dexheimer, N; Besche, V et al.
Mutated cylindromatosis gene affects the functional state of dendritic cellsEUROPEAN JOURNAL OF IMMUNOLOGY. Bd. 40. H. 10. 2010 S. 2848-2857
Zechner, U; Hermanns, P; Keilmann, A et al.
Mutation analysis of the SLC26A4 gene in 133 patients from Germany with nonsyndromic hearing loss. 21.Jahrestagung Humangenetik,Hamburg,02.-04.03.2010MEDIZINISCHE GENETIK. Bd. 22. H. 1. 2010 S. 126
Hov, JR; Keitel, V; Laerdahl, JK et al.
Mutational Characterization of the Bile Acid Receptor TGR5 in Primary Sclerosing CholangitisPLOS ONE. Bd. 5. H. 8. 2010 S. -
Ivaskevicius, V; Biswas, A; Loreth, R et al.
Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiencyHAEMOPHILIA. Bd. 16. H. 4. 2010 S. 675-682
Pulvers, JN; Bryk, J; Fish, JL et al.
Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germlinePROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. Bd. 107. H. 38. 2010 S. 16595-16600
Hermanns, P; Grasberger, H; Refetoff, S et al.
Mutations in the NKX2.5 gene and in the PAX8 promoter cause congenital hypothyroidism in a girl with thyroid dysgenesis. 49(th) Meeting of the European Society for Pediatric Endocrinology, PragueHORMONE RESEARCH. Bd. 74. H. Spl3. 2010 S. 90
Gramley, F; Kettering, K; Koellensperger, E et al.
Myocardial fibrosis in a canine model of combined congestive heart failure and atrial fibrillationEUROPEAN HEART JOURNAL. Bd. 31. 2010 S. 1041-1041
Claeys, KG; Pellissier, JF; Garcia-Bragado, F et al.
Myopathy with hexagonally cross-linked crystalloid inclusions: Delineation of a clinico-pathological entityNEUROMUSCULAR DISORDERS. Bd. 20. H. 11. 2010 S. 701-708