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Molecular Genetic Analysis of SLC3A1 and SLC7A9 Genes in Czech and Slovak Cystinuric Patients

Annals of human genetics, 2005-09, Vol.69 (5), p.501-507

2005

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Presence of a deletion in the 5′ upstream region of the GALT gene in Duarte (D2) alleles

Journal of medical genetics, 1999-07, Vol.36 (7), p.576-578

1999

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First Report of a Multicenter Prospective Registry of Cranioplasty in the United Kingdom and Ireland

Neurosurgery, 2021-09, Vol.89 (3), p.518-526

2021

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International Tuberculum Sellae Meningioma Study: Surgical Outcomes and Management Trends

Neurosurgery, 2023-12, Vol.93 (6), p.1259-1270

2023

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International Tuberculum Sellae Meningioma Study: Preoperative Grading Scale to Predict Outcomes and Propensity-Matched Outcomes by Endonasal Versus Transcranial Approach

Neurosurgery, 2023-12, Vol.93 (6), p.1271-1284

2023

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Maternal hyperphenylalaninemias in healthy Czech population of pregnant women: 30 years experience with screening, prevention and treatment

Bratislavské lékarské listy, 2004, Vol.105 (9), p.291

2004

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Targeted metabolomics for diagnosing of inherited metabolic disorders

Clinical biochemistry, 2011-05, Vol.44 (7), p.520-520

2011

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Carbapenemase-producing Klebsiella pneumoniae in the Czech Republic in 2011

Euro surveillance : bulletin européen sur les maladies transmissibles, 2013-11, Vol.18 (45), p.20626-20626

2013

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Evaluation of MP4OX for prevention of perioperative hypotension in patients undergoing primary hip arthroplasty with spinal anesthesia: a randomized, double-blind, multicenter study

Anesthesiology (Philadelphia), 2011-05, Vol.114 (5), p.1048-1063

2011

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A double-blind, randomized, multicenter study of MP4OX for treatment of perioperative hypotension in patients undergoing primary hip arthroplasty under spinal anesthesia

Anesthesia and analgesia, 2011-04, Vol.112 (4), p.759-773

2011

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Identification of three novel mutations in the PHKA2 gene in Czech patients with X‐linked liver glycogenosis

Journal of inherited metabolic disease, 2001-02, Vol.24 (1), p.85-87

2001

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Mutation and haplotype analysis of phenylalanine hydroxylase alleles in classical PKU patients from the Czech Republic: identification of four novel mutations

Journal of medical genetics, 1997-11, Vol.34 (11), p.893-898

1997

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Racism and Ethnic Inequality in a Time of Crisis: Findings from the Evidence for Equality National Survey

2023

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Mutation analysis of the GALT gene in Czech and Slovak galactosemia populations: Identification of six novel mutations, including a stop codon mutation (X380R)

Human mutation, 2000-02, Vol.15 (2), p.206-206

2000

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Identification of mutations in the glucose-6-phosphatase gene in Czech and Slovak patients with glycogen storage disease type Ia, including novel mutations K76N, V166A and 540del5

Human mutation, 2000-07, Vol.16 (1), p.89-89

2000

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Anthropologic study of women with hyperphenylalaninemia

Ceská gynekologie, 2002-07, Vol.67 (4), p.215

2002

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Sexual life of women with hyperphenylalaninemia

Ceská gynekologie, 2002-05, Vol.67 (3), p.171

2002

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Is the anti-selection initiative in reproductive medicine anti-biological?

Ceská gynekologie, 1997-08, Vol.62 (4), p.233

1997

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Mutation of the phenylalanine hydroxylase gene in the population of central Bohemia. Relation to the clinical picture of phenylketonuria

Časopis lékařů českých, 1997-05, Vol.136 (9), p.282

1997

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The Role of Proteomics in Identification of Key Proteins of Bacterial Cells with Focus on Probiotic Bacteria

International journal of molecular sciences, 2024-08, Vol.25 (16), p.8564

Stastna, Miroslava

2024

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Advances in separation and identification of biologically important milk proteins and peptides

Electrophoresis, 2024-01, Vol.45 (1-2), p.101-119

Stastna, Miroslava

2024

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Post-translational modifications of proteins in cardiovascular diseases examined by proteomic approaches

The FEBS journal, 2024-03

Stastna, Miroslava

2024

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Proteomics as a Tool for the Study of Mitochondrial Proteome, Its Dysfunctionality and Pathological Consequences in Cardiovascular Diseases

International journal of molecular sciences, 2023-02, Vol.24 (5), p.4692

Stastna, Miroslava

2023

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Continuous flow electrophoretic separation — Recent developments and applications to biological sample analysis

Electrophoresis, 2020-01, Vol.41 (1-2), p.36-55

Stastna, Miroslava

2020

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Maternal hyperphenylalaninemia in a population of healty Czech women. 18 years' experience with mass screening, diet therapy and metabolic monitoring

Časopis lékařů českých, 1996-01, Vol.135 (2), p.50

1996

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Molecular Genetic Analysis of SLC3A1 and SLC7A9 Genes in Czech and Slovak Cystinuric Patients

Presence of a deletion in the 5′ upstream region of the GALT gene in Duarte (D2) alleles

First Report of a Multicenter Prospective Registry of Cranioplasty in the United Kingdom and Ireland

International Tuberculum Sellae Meningioma Study: Surgical Outcomes and Management Trends

International Tuberculum Sellae Meningioma Study: Preoperative Grading Scale to Predict Outcomes and Propensity-Matched Outcomes by Endonasal Versus Transcranial Approach

Maternal hyperphenylalaninemias in healthy Czech population of pregnant women: 30 years experience with screening, prevention and treatment

Targeted metabolomics for diagnosing of inherited metabolic disorders

Carbapenemase-producing Klebsiella pneumoniae in the Czech Republic in 2011

Evaluation of MP4OX for prevention of perioperative hypotension in patients undergoing primary hip arthroplasty with spinal anesthesia: a randomized, double-blind, multicenter study

A double-blind, randomized, multicenter study of MP4OX for treatment of perioperative hypotension in patients undergoing primary hip arthroplasty under spinal anesthesia

Identification of three novel mutations in the PHKA2 gene in Czech patients with X‐linked liver glycogenosis

Mutation and haplotype analysis of phenylalanine hydroxylase alleles in classical PKU patients from the Czech Republic: identification of four novel mutations

Racism and Ethnic Inequality in a Time of Crisis: Findings from the Evidence for Equality National Survey

Mutation analysis of the GALT gene in Czech and Slovak galactosemia populations: Identification of six novel mutations, including a stop codon mutation (X380R)

Identification of mutations in the glucose-6-phosphatase gene in Czech and Slovak patients with glycogen storage disease type Ia, including novel mutations K76N, V166A and 540del5

Anthropologic study of women with hyperphenylalaninemia

Sexual life of women with hyperphenylalaninemia

Is the anti-selection initiative in reproductive medicine anti-biological?

Mutation of the phenylalanine hydroxylase gene in the population of central Bohemia. Relation to the clinical picture of phenylketonuria

The Role of Proteomics in Identification of Key Proteins of Bacterial Cells with Focus on Probiotic Bacteria

Advances in separation and identification of biologically important milk proteins and peptides

Post-translational modifications of proteins in cardiovascular diseases examined by proteomic approaches

Proteomics as a Tool for the Study of Mitochondrial Proteome, Its Dysfunctionality and Pathological Consequences in Cardiovascular Diseases

Continuous flow electrophoretic separation — Recent developments and applications to biological sample analysis

Maternal hyperphenylalaninemia in a population of healty Czech women. 18 years' experience with mass screening, diet therapy and metabolic monitoring

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