Contents
Physiol. Res. 55: S1, 2006
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Foreword
P. Martásek
Minireviews:
Physiol. Res. 55: S3-S26, 2006
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Quo vadis porphyrin chemistry?
V. Král, J. Králová, R. Kaplánek, T. Bříza, P. Martásek (Dept.
Anal. Chem., Inst. Chem. Technology, Prague, Czech Republic)
Physiol. Res. 55: S27-S41, 2006
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Biogenesis of eukaryotic cytochrome c oxidase.
L. Stiburek, H. Hansikova, M. Tesarova, L. Cerna, J. Zeman (Dept
Pediat, Ctr Appl Genomics, 1st Fac. Med., Charles Univ., Prague,
Czech Republic
Physiol. Res. 55: S43-S66, 2006
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(Far) Outside the box: Genomic approach to acute porphyria.
S. Thunell (Ctr Inborn Metabol Disorders, Karolinska Univ
Hospital Huddinge, Stockholm Sweden)
Physiol. Res. 55: S67-S73, 2006
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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
(Ctr Français des Porphyries, Hôpital Louis Mourier, Colombes
CEDEX, France) S67
Physiol. Res. 55: S75-S83, 2006
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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 (Dept Int. Med. I, Univ Hospital Bonn, Bonn,
Germany)
Physiol. Res. 55: S85-S92, 2006
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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 (Afdeling Dermatol., Academisch
Ziekenhuis Maastricht, Maastricht; The Netherlands)
Physiol. Res. 55: S93-S101, 2006
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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 (Unité de Génétique des Mammifères, Institut
Pasteur, Paris, France)
Physiol. Res. 55: S103-S108, 2006
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Individualized workup - a new approach to the biochemical
diagnosis of acute attacks of neuroporphyria.
N. Schoenfeld, R. Mamet (Porphyria Reference Lab, Rabin Med Ctr,
Campus Beilinson, Petah- Tikva, Israel)
Physiol. Res. 55: S109-S118, 2006
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Porphyria in Sweden.
S. Thunell, Y. Floderus, A. Henrichson, P. Harper (Porphyria Ctr
Sweden, Karolinska Univ Hospital Huddinge, Stockholm, Sweden)
Physiol. Res. 55: S119-S136, 2006
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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 (Dept Pediat, School Med,
Charles Univ, Prague, Czech Republic)
Physiol. Res. 55: S137-S144, 2006
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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 (Dept. Int. Med.
I, Univ Hospital Bonn, Bonn, Germany)
Physiol. Res. 55: S145-S154, 2006
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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 (Dept. Pediatrics, 1st Fac. of Medicine,
Charles Univ., Prague, Czech Rep., 2nd Pediatric Dept.,
Children’s Faculty Hospital, Košice, Slovak Republic)
Short Communication
Physiol. Res. 55: S155-S157, 2006
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The difficult clinical diagnosis of erythropoietic
protoporphyria.
S. Wahlin, Y. Floderus, A-M Ros, U. Broomé, P. Harper (Porphyria
Ctr Sweden, Karolinska Univ Hospital Huddinge, Stockholm,
Sweden)
This number was issued in December 2006
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