J. Hyánek

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Patients with Abdominal Aortic Aneurysm Demonstrate Higher Levels of Non-cholesterol Sterol Markers of Endogenous Cholesterol Synthesis

M. Prucha, F. Pehal, P. Štádler, 2017 .

Lathosterol and other Noncholesterol Sterols in Treatment of Hereditary Hypercholesterolemias: 20-Year Experience among School Children and Adolescents

F. Pehal, B. Míková, L. Dubská, 2018, Journal of Nutritional Therapeutics.

Essential hypertension in adolescents: association with insulin resistance and with metabolism of homocysteine and vitamins.

J. Zvárová, K. Zvára, V. Kožich, 2002, American journal of hypertension.

Profiling of amino acids in body fluids and tissues by means of liquid chromatography.

Z. Deyl, J. Hyánek, M. Horáková, 1986, Journal of chromatography.

Iminoglycinuria in a child in Czechoslovakia

J. Jirásek, J. Hyánek, B. Blehová, 1973, Humangenetik.

Chromatographic screening for cystinuria among newborns

J. Hyánek, 1980, Journal of Inherited Metabolic Disease.

Gestational hypercholesterolemia helps detect familial hypercholesterolemia and prevent late pregnancy complications

K. Dryahina, M. Prucha, F. Pehal, 2019, Clinical Journal of Obstetrics and Gynecology.

Is the common 844ins68 polymorphism in the cystathionine β-synthase gene associated with atherosclerosis?

J. Zvárová, J. Kraus, M. Štefek, 1999, Journal of Inherited Metabolic Disease.

[Non-ketotic hyperglycinemia].

J. Zeman, V. Kožich, J. Hoza, 1990, Ceskoslovenska pediatrie.

Typical hyperaminoaciduria after high doses of 6-azauridine triacetate.

M. Slavik, J. Homolka, J. Hyánek, 1969, Biochemical pharmacology.

Vascular presentation of cystathionine beta-synthase deficiency in adulthood

J. Zeman, T. Honzík, V. Kožich, 2010, Journal of Inherited Metabolic Disease.

Genetic variants of homocysteine metabolizing enzymes and the risk of coronary artery disease.

J. Zvárová, V. Kožich, M. Andel, 2003, Molecular genetics and metabolism.

“Peripheral” tetrahydrobiopterin deficiency with hyperphenylalaninaemia due to incomplete 6-pyruvoyl tetrahydropterin synthase deficiency or heterozygosity

J. Zeman, H. Shintaku, W. Endres, 1987, European Journal of Pediatrics.

Facts and artefacts in mevalonic aciduria: development of a stable isotope dilution GCMS assay for mevalonic acid and its application to physiological fluids, tissue samples, prenatal diagnosis and carrier detection.

H. Bremer, W. Nyhan, F. Trefz, 1991, Clinica chimica acta; international journal of clinical chemistry.

'Homocystinuria' and urinary excretion of beta-amino acids in patients treated with 6-azauridine.

H. Bremer, M. Slavik, J. Hyánek, 1969, Clinica chimica acta; international journal of clinical chemistry.

Accumulation and impaired in vivo metabolism of di- and trihydroxycholestanoic acid in two patients.

R. Schutgens, J. Zeman, R. Wanders, 1991, Clinica chimica acta; international journal of clinical chemistry.

The effect of insulin load on plasma tryptophan levels in schizophrenic patients.

L. Haškovec, J. Hyánek, V. Filip, 1974, Activitas nervosa superior.

Cerebrospinal fluid.

P. Adam, O. Sobek, M. Prucha, 2001, Advances in Clinical Chemistry.

Relationships between rutting behaviour and non-annual incisor dentine layers of male sika deer - a hypothesis

L. Bartoš, J. Hyánek, V. Malik, 1984 .

Subclinical course of cholesteryl ester storage disease in an adult with hypercholesterolemia, accelerated atherosclerosis, and liver cancer.

A. Chlumská, S. Maas, M. Elleder, 2000, Journal of hepatology.

Complete proteinogram of cerebrospinal fluid and its contribution to the diagnostics of inflammatory and autoimmune diseases of the central nervous system.

B. Veselá, P. Adam, O. Sobek, 2003, Sbornik lekarsky.

Results of screening for phenylalanine and other amino acid disturbances among pregnant women

E. Seemanová, J. Trnka, J. Homolka, 1979, Journal of Inherited Metabolic Disease.

Speech and language disorders in histidinaemia and other amino acid disturbances

J. Hyánek, V. Raisová, 1985, Journal of Inherited Metabolic Disease.

Changes in phenylalanine tolerance while monitoring the dietetic treatment of pregnant women suffering from hyperphenylalaninaemia

J. Kobilková, J. Soukup, J. Hyánek, 1988, Journal of Inherited Metabolic Disease.

Studies of blood and breast milk amino acid concentrations in mothers with abnormal phenylalanine metabolism

J. Kobilková, J. Hyánek, M. Kubík, 1983, Journal of Inherited Metabolic Disease.

Oculocerebrorenal syndrome in a female child.

A. Komárková, J. Hyánek, J. Švorc, 1967, American journal of diseases of children.

Lathosterol and Noncholesterol Sterols in Routine Use for the Differentiation and Monitoring of Dietary and Drug Induced Treatment of Hypercholesterolemias in Children and Adolescents

F. Pehal, L. Dubská, J. Hyánek, 2014 .

Significance of lipopolysaccharide-binding protein (an acute phase protein) in monitoring critically ill patients

M. Dostál, R. Zazula, M. Prucha, 2003, Critical care.

Moderate hyperhomocysteinemia in patients treated for epilepsy.

J. Dvořáková, M. Kolínová, J. Hyánek, 2006, Prague medical report.

Mevalonic aciduria

K. Gibson, J. Zeman, V. Kožich, 1991, Journal of Inherited Metabolic Disease.

Genetic determinants of folate status in Central Bohemia.

J. Zvárová, V. Kožich, M. Andel, 2005, Physiological research.

Effect of pravastatin on plasma concentrations of homocysteine in primary hypercholesterolemia

J. Dvořáková, L. Dubská, J. Hyánek, 2001 .

Intellectual and school performance in adolescents with phenylketonuria according to their dietary compliance

J. Zeman, A. Pijáčková, J. Hyánek, 2009, European Journal of Pediatrics.

[Homocysteinemia and ovariectomy--initial experience with functional monitoring].

J. Živný, A. Kapral, T. Fait, 2002, Ceska gynekologie.

Urinary pterins in Lesch-Nyhan syndrome.

S. Kmoch, J. Krijt, I. Šebesta, 1991, Advances in Experimental Medicine and Biology.

Unusual clinical presentation in two boys with cytochrome c oxidase deficiency.

R. Wanders, J. Zeman, J. Ruiter, 1992, Journal of inherited metabolic disease.