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Czech-Slovak Pediatrics - Issue 6/2018
348Characteristic clinical features and laboratory findings of inborn errors of metabolismH. Kolářová, T. Honzík
365Phosphomannomutase 2 deficiency: clinical, biochemical and molecular analyses in 22 Czech patientsA. Čechová, N. Ondrušková, M. Tesařová, H. Hansíková, J. Zeman, T. Honzík
375A complex view of vitamin B12 deficiency in childhoodK. Brennerová, K. Juríčková, C. Šebová, M. Ostrožlíková, J. Hornová, M. Kolníková, V. Bzdúch
384Barth syndrome – case historyS. Tárnoková, C. Šebová, K. Brennerová, J. Perečková, P. Kunovský, R. Riedel, M. Ďuranová, V. Bzdúch
390Newborn screening of inherited metabolic diseases in the Czech RepublicK. Pešková, P. Chrastina, J. Bártl, T. Adam, F. Votava, T. Honzík, V. Kožich
395Nutritional therapy in patients with inherited metabolic disordersM. Floriánková, Š. Bláhová, M. Pencová, T. Honzík, P. Ješina
408Lysosomal storage disorders – development of diagnostic process and treatment in SlovakiaK. Juríčková, S. Mattošová, A. Šalingová, P. Jungová, K. Brennerová, M. Kolníková, Ľ. Košťálová, A. Hlavatá
Czech-Slovak Pediatrics
2018 Issue 6
Most read in this issue- Characteristic clinical features and laboratory findings of inborn errors of metabolism
- A complex view of vitamin B12 deficiency in childhood
- Newborn screening of inherited metabolic diseases in the Czech Republic
- Lysosomal storage disorders – development of diagnostic process and treatment in Slovakia
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