A decrease in serum 1,25(OH)2D after elective hip replacement and during bone healing is associated with changes in serum iron and plasma FGF23 von Vaculik, J., Wenchich, L., Bobelyak, M., Pavelka, K., Stepan, J. J.

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Decrease in serum calcitriol (but not free 25-hydroxyvitamin D) concentration in hip fracture healing von Vaculik, J., Wenchich, L., Bobelyak, M., Pavelka, K., Stepan, J. J.

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The Effect of Very-Low-Calorie Diet on Mitochondrial Dysfunction in Subcutaneous Adipose Tissue and Peripheral Monocytes of Obese Subjects with Type 2 Diabetes Mellitus von URBANOVÁ, M., MRÁZ, M., ĎUROVCOVÁ, V., TRACHTA, P., KLOUČKOVÁ, J., KAVÁLKOVÁ, P., HALUZÍKOVÁ, D., LACINOVÁ, Z., HANSÍKOVÁ, H., WENCHICH, L., KRŠEK, M., HALUZÍK, M.

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Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates von Honzik, T, Wenchich, L, Böhm, M, Hansikova, H, Pejznochova, M, Zapadlo, M, Plavka, R, Zeman, J

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Fumaric aciduria: Mild phenotype in a 8‐year‐old girl with novel mutations von Maradin, M., Fumić, K., Hansikova, H., Tesarova, M., Wenchich, L., Dorner, S., Sarnavka, V., Zeman, J., Barić, I.

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A decrease in serum 1,25(OH) 2 D after elective hip replacement and during bone healing is associated with changes in serum iron and plasma FGF23 von Vaculik, J, Wenchich, L, Bobelyak, M, Pavelka, K, Stepan, J J

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Two patients with clinically distinct manifestation of pyruvate dehydrogenase deficiency due to mutations in PDHA1 gene von Magner, M, Vinšová, K, Tesařová, M, Hájková, Z, Hansíková, H, Wenchich, L, Ješina, P, Smolka, V, Adam, T, Vaněčková, M, Zeman, J, Honzík, T

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The relationship of mitochondrial dysfunction and the development of insulin resistance in Cushing's syndrome von Ježková, Jana, Ďurovcová, Viktória, Wenchich, Laszlo, Hansíková, Hana, Zeman, Jiří, Hána, Václav, Marek, Josef, Lacinová, Zdeňka, Haluzík, Martin, Kršek, Michal

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Mitochondrial DNA Depletion in Alpers Syndrome von Tesarova, M., Mayr, J. A., Wenchich, L., Hansikova, H., Elleder, M., Blahova, K., Sperl, W., Zeman, J.

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Polarographic evaluation of mitochondrial enzymes activity in isolated mitochondria and in permeabilized human muscle cells with inherited mitochondrial defects von Wenchich, L, Drahota, Z, Honzík, T, Hansíková, H, Tesarová, M, Zeman, J, Houstek, J

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Abnormalities in succinylpurines in fumarase deficiency: Possible role in pathogenesis of CNS impairment von Zeman, J., Krijt, J., Stratilová, L., Hansíková, H., Wenchich, L., Kmoch, S., Chrastina, P., Houštěk, J.

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44 Knockdown of Cox6a subunit leads to decreased affinity for oxygen of cytochrome c oxidase von Wenchich, L., Fornuskova, D., Stiburek, L., Vinsova, K., Hansikova, H., Zeman, J.

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Knockdown of Human Oxa1l Impairs the Biogenesis of F sub(1)F sub(o)-ATP Synthase and NADH:Ubiquinone Oxidoreductase von Stiburek, L, nuskova, D, Wenchich, L, Pejznochova, M, Hansikova, H, Zeman, J

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Posterior Reversible Encephalopathy Syndrome (PRES) in 5-year-old girl with nephrotic syndrome von Kabicek, Pavel, Sulek, Stepan, Seidl, Zdenek, Vaneckova, Manuela, Kabickova, Edita, Vobruba, Vaclav, Wenchich, Laszlo, Zeman, Jiri

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Mitochondrial Energy Metabolism in Very Premature Neonates von Wenchich, László, Zeman, Jiří, Hansíková, Hana, Plavka, Richard, Sperl, Wolfgang, Houštěk, Josef

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Novel mutations in a boy with dihydrolipoamide dehydrogenase deficiency von Cerna, L, Wenchich, L, Hansiková, H, Kmoch, S, Peskova, K, Chrastina, P, Brynda, J, Zeman, J

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Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) von Honzík, T, Tesarová, M, Hansíková, H, Krijt, J, Benes, P, Zámecník, J, Wenchich, L, Zeman, J

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Mitochondrial DNA Depletion in Alpers Syndrome von Tesarova, M., Mayr, J. A., Wenchich, L., Hansikova, H., Elleder, M., Blahova, K., Sperl, W., Zeman, J.

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The effect of very-low-calorie diet on mitochondrial dysfunction in subcutaneous adipose tissue and peripheral monocytes of obese subjects with type 2 diabetes mellitus von Urbanová, M, Mráz, M, Ďurovcová, V, Trachta, P, Kloučková, J, Kaválková, P, Haluzíková, D, Lacinová, Z, Hansíková, H, Wenchich, L, Kršek, M, Haluzík, M

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