[Familial hyperlipoproteinemia type IIA with homozygotic manifestations in a heterozygote]

[Hyperlipoproteinaemia and dyslipoproteinaemia I. Classification, diagnostics, cardiovascular, cardiometabolic and residual risk].

Vnitrni lekarstvi·2010

[Familial hyperlipoproteinemias--correlations between phenotypes and genotypes].

Casopis lekaru ceskych·2001

[Genetic predisposition for multiple metabolic syndrome. Part 1. Diabetes mellitus type 2--incidence and prevalence].

Casopis lekaru ceskych·2000

The effect of four-year hypolipidaemic treatment on the intimal thickness of the common carotid artery in patients with familiar hyperlipidaemia.

International angiology : a journal of the International Union of Angiology·2000

[Negative aspects of the Western life style and possibilities of intervention in patients with familial combined hyperlipidemia].

Casopis lekaru ceskych·1999

[Genetic predisposition for the multiple metabolic syndrome. Part 4. Apolipoprotein E and lipoprotein (a)].

Casopis lekaru ceskych·1999

Pharmacological profile of mepolizumab.

Vnitrni lekarstvi·2023

Atypical form of Goodpasture's disease.

Vnitrni lekarstvi·2023

Differentiated thyroid cancer - possible risks of treatment, suppressive therapy and adherence to current recommendations.

Vnitrni lekarstvi·2023

Dyslipidemia - the known unknown.

Vnitrni lekarstvi·2023

Internal comorbidities and complications of multiple sclerosis therapy - don't be caught off guard!

Vnitrni lekarstvi·2023

Implications of highly suppressive treatment HIV infection.

Vnitrni lekarstvi·2023

The clock-output gene DBP regulates muscle insulin sensitivity and its fluctuations.

Journal of diabetes investigation·2026

Genetic variants shape single-cell chromatin accessibility and disease risk.

Nature·2026

Population-scale single-nucleus multi-omic profiling of skeletal muscle reveals extensive context-specific genetic regulation.

Nature genetics·2026

Hippocampal Subfield Volumes and Spatial Memory Performance in Older Adults At-Risk for Type 2 Diabetes.

Hippocampus·2026

[Inherited anemias: current approaches to diagnosis and treatment].

[Rinsho ketsueki] The Japanese journal of clinical hematology·2026

Application of array comparative genomic hybridization on the DNA extracted from neonatal buccal mucosal cells for the postnatal investigation of prenatally detected chromosomal mosaicism at amniocentesis.

Taiwanese journal of obstetrics & gynecology·2026

[Familial hyperlipoproteinemia type IIA with homozygotic manifestations in a heterozygote]

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[Hyperlipoproteinaemia and dyslipoproteinaemia I. Classification, diagnostics, cardiovascular, cardiometabolic and residual risk].

[Familial hyperlipoproteinemias--correlations between phenotypes and genotypes].

[Genetic predisposition for multiple metabolic syndrome. Part 1. Diabetes mellitus type 2--incidence and prevalence].

The effect of four-year hypolipidaemic treatment on the intimal thickness of the common carotid artery in patients with familiar hyperlipidaemia.

[Negative aspects of the Western life style and possibilities of intervention in patients with familial combined hyperlipidemia].

[Genetic predisposition for the multiple metabolic syndrome. Part 4. Apolipoprotein E and lipoprotein (a)].

Pharmacological profile of mepolizumab.

Atypical form of Goodpasture's disease.

Differentiated thyroid cancer - possible risks of treatment, suppressive therapy and adherence to current recommendations.

Dyslipidemia - the known unknown.

Internal comorbidities and complications of multiple sclerosis therapy - don't be caught off guard!

Implications of highly suppressive treatment HIV infection.

The clock-output gene DBP regulates muscle insulin sensitivity and its fluctuations.

Genetic variants shape single-cell chromatin accessibility and disease risk.

Population-scale single-nucleus multi-omic profiling of skeletal muscle reveals extensive context-specific genetic regulation.

Hippocampal Subfield Volumes and Spatial Memory Performance in Older Adults At-Risk for Type 2 Diabetes.

[Inherited anemias: current approaches to diagnosis and treatment].

Application of array comparative genomic hybridization on the DNA extracted from neonatal buccal mucosal cells for the postnatal investigation of prenatally detected chromosomal mosaicism at amniocentesis.

[Familial hyperlipoproteinemia type IIA with homozygotic manifestations in a heterozygote]

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