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Volume 55, Suppl 2, 2006 | |
Physiol. Res. 55: S1, 2006 Full text Foreword P. Martásek MINIREVIEW Physiol. Res. 55: S3-S26, 2006 ; doi: 10.33549/physiolres.930000.55.S2.3 Full text Quo vadis porphyrin chemistry? V. Král, J. Králová, R. Kaplánek, T. Bříza, P. Martásek
Biogenesis of eukaryotic cytochrome c oxidase L. Stiburek, H. Hansikova, M. Tesarova, L. Cerna, J. Zeman (Far) Outside the box: Genomic approach to acute porphyria S. Thunell
ORIGINAL ARTICLES Physiol. Res. 55: S67-S73, 2006; doi: 10.33549/physiolres.930000.55.S2.67 Full text European porphyria initiative (EPI): a platform to develop a common approach to the management of porphyrias and to promote research in the field J.-Ch. Deybach, M. Badminton, H. Puy, S.
Sandberg, J. Frank, P. Harper, P. Martasek, E. Minder, S.
Parker, S. Thunell G. Elder
Physiol. Res. 55: S75-S83, 2006; doi: 10.33549/physiolres.930000.55.S2.75 Full text Hemochromatosis gene sequence deviations in German patients with porphyria cutanea tarda J. Frank, P. Poblete-Gutiérrez, R. Weiskirchen, O. Gressner, H.
F. Merk, F. Lammert Identification of mutations in the uroporphyrinogen iii cosynthase gene in German patients with congenital erythropoietic porphyria T. Wiederholt, P. Poblete-Gutiérrez, K. Gardlo, G. Goerz, K.
Bolsen, H. F. Merk, J. Frank
Physiol. Res. 55: S93-S101, 2006; doi: 10.33549/physiolres.930000.55.S2.93 Full text Ursodesoxycholic acid and heme-arginate are unable to improve hematopoiesis and liver injury in an erythropoietic protoporphyria mouse model M. Abitbol, H. Puy, J-M Sabaté, J-L Guénet, J-Ch Deybach, X.
Montagutelli Individualized workup - a new approach to the biochemical diagnosis of acute attacks of neuroporphyria N. Schoenfeld, R. Mamet Porphyria in Sweden S. Thunell, Y. Floderus, A. Henrichson, P. Harper
May 2006 update in porphobilinogen deaminase gene polymorphisms and mutations causing acute intermittent porphyria. Comparison with the situation in Slavic population M. Hrdinka, H. Puy, P. Martásek
Demystification of Chester porphyria: A nonsense mutation in the porphobilinogen deaminase gene P. Poblete-Gutiérrez, T. Wiederholt, A. Martinez-Mir, H. F.
Merk, J. M. Connor, A. M. Christiano, J. Frank
De novo mutation found in the porphobilinogen deaminase gene in Slovak acute intermittent porphyria patient: Molecular biochemical study D. Ulbrichova, E. Flachsova, M. Hrdinka, J. Saligova, J. Bazar,
C.S. Raman, P. Martasek SHORT COMMUNICATION The difficult clinical diagnosis of erythropoietic protoporphyria S. Wahlin, Y. Floderus, A-M Ros, U. Broomé, P. Harper
This number was issued in December 2006 |
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© 2006 by the Institute of Physiology, Czech Academy of Sciences |