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E. Malonova
E. Malonova
Medicine
Internal medicine
Diabetes mellitus
Transferrin
Molecular biology
4
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26
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[Congenital disorder of type Ia protein glycosylation: clinical, biochemical and molecular characteristics in 2 siblings with cerebellar hypoplasia].
2003
Casopís lékar̆ů c̆eských
Tomas Honzik
E. Malonova
Hansíková H
Rosipal R
Poupĕtová H
Martásek P
Jiri Zeman
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Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT)
2002
Cellular and Molecular Biology
Jérôme Lamoril
Christophe Andant
Laurent Gouya
E. Malonova
Bernard Grandchamp
Pavel Martásek
Deybac Jc
Hervé Puy
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“Homozygous” variegate porfyria
2001
Journal of Hepatology
E. Malonova
Anne–Marie Robreau
Jiri Zeman
Hervé Puy
V. Da Silva
R. Rosipal
Martásek P
Jean-Charles Deybach
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In frame deletion of glycin 390 in coproporphyrinogen oxidase gene as a cause of hereditary coproporphyria
2001
Journal of Hepatology
R. Rosipal
E. Malonova
Jiri Zeman
Jean-Charles Deybach
Jérôme Lamoril
Pavel Martásek
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