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CZECH MEDICAL ASSOCIATION J. Ev. PURKYNĚ |
| Journals - Contents | |
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Česko-slovenská pediatrie |
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Sinigerska I., Simeonov E., Vladimirova K., Radeva B., Tincheva R.:
Biochemical Diagnosis of Lysosomal Storage Diseases. Revue of 8-year Experience |
411 |
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Matalon R., Rady S., Szucs K., Matalon P., Hyánek J., Šebesta P.,Matoušková J., Vondráčková N., Pejznochová H., Dubská L., Přindisová H., Dvořáková J., Loučka M., Martiniková V., Šlancová M.:
Polymorphism of MTHFR and MTRR in Czech Patients with Cardiovascular Diseases and Stroke |
418 |
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Strnová J.1. Ürge O.2, Beránková M.1:
Organization of the Care of Patients with Hyperphenylalaninemia in Slovakia |
421 |
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Marklová E., Albahri Z.:
Methodic Guide to Diagnostics of Congenital Disorders of Glycosylation (CDG) |
423 |
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Ürge O.1, Strnová J.2, Mosendzová B.1:
Phenylketonuria in Adolescents and Adult Persons in Slovakia |
423 |
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Bzdúch V.1, Behúlová D.2, Fabriciová K.1, Šalingová A.2, Šaligová J.3,Šťastná S.4, LehnertW.5, Sass J. O.5, Kozák L.6, Benedeková M.1:
MCAD Deficiency - Our Experience with Four Symptomatic Patients |
430 |
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Stožický F.1, Šebková A.2, Pečenková R.2, Liška J.3:
Selective Screening of Children at Risk of Early Atherosclerosis in the Czech Republic |
433 |
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Šťastná S.1, PeškováK.1, EllederM.1, PoupětováH.1, Hlavatá A.2,Mišovicová N.3:
Glycogenosis Type II - Infantile Form (Morbus Pompe) in the Czech and Slovak Population |
436 |
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Vaďurová L.1, Šťastná S.1, Hyánek J.1,2:
Aspects of Psychological Care of Patients with Phenylketonuria |
441 |
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Behúlová D.1, Fabriciová K.2, Bzdúch V.2, Buzassyová D.3, Škodová J.1,Šalingová A.1, Vasilenková A.1, Ponec J.1 :
Unusual Cause of Severe Lactate Acidosis in a Seven-month Child |
447 |
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Šaligová J.1, Potočňáková Ľ.1, Bratský L.2, Figulová E.2, Fedorová E.1:
Analysis of Consequences of Phenylketonuria in Relation to Metabolic Compensation and Age |
451 |
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Honzík T., Hansíková H., Flachsová E., Rosipal R., Poupětová H.2,:
Clinical and Molecular Analyses in Eight Children with Congenital Disorders of Glycosylation |
456 |
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Vepřeková L.1, Starý J.2, Buncová M.3, Vitnerová L.4, Hrubá E.4,Toušovská K.5, Zeman J.4:
Megaloblastic Anemia 1 (Imerslund-Gräsbeck) |
461 |
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Chrastina P., Šťastná S., Myšková H., Zeman J.:
Tandem Mass Spectrometry - The Future of Newborn Screening of Inborn Errors of Metabolism |
464 |
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