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A rare cause of mediastinal expansion with a massive pleural effusion

Postgraduate medical journal, 2005-11, Vol.81 (961), p.e18-e18

2005

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The expression of PAX5, p53 immunohistochemistry and p53 mutation analysis in superficial bladder carcinoma tissue. Correlation with pathological findings and clinical outcome

International urology and nephrology, 2002, Vol.34 (4), p.495-501

2002

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The human genome and medicine

Časopis lékařů českých, 2002, Vol.141 (1), p.8

Sedlácek, Z

2002

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Non-linear free streaming in Vlasov plasma

Czechoslovak journal of physics, 2004-01, Vol.54 (S3), p.C82-C88

Sedláček, Z.

2004

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A database of germline p53 mutations in cancer-prone families

Nucleic acids research, 1998-01, Vol.26 (1), p.214-215

1998

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Oncogene amplification and expression in pediatric solid tumors

Neoplasma, 1998, Vol.45 (3), p.123

1998

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When is it useful to look for TP53 germline gene mutations in families of oncology patients?

Časopis lékařů českých, 2003, Vol.142 (4), p.220

2003

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Two Li-Fraumeni syndrome families with novel germline p53 mutations : loss of the wild-type p53 allele in only 50% of tumours

British journal of cancer, 1998-04, Vol.77 (7), p.1034-1039

1998

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The amphioxus rab GDP-dissociation inhibitor (GDI) gene is neural-specific: implications for the evolution of chordate rab GDI genes

Molecular biology and evolution, 1999-09, Vol.16 (9), p.1231-1237

1999

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The human genome--chromosome X. Focus on Xq28

Časopis lékařů českých, 1995-12, Vol.134 (23), p.760

Sedlácek, Z

1995

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Genetics of autism

Časopis lékařů českých, 2002-06, Vol.141 (12), p.376

2002

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Not EEG abnormalities but epilepsy is associated with autistic regression and mental functioning in childhood autism

European child & adolescent psychiatry, 2004-08, Vol.13 (4), p.209-213

2004

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Stationary equilibria of a collisionless plasma treated by the moment method

Plasma physics, 1967-01, Vol.9 (3), p.255-274

Sedlácek, Z

1967

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SECURITY QUESTIONS OF THE USE OF SMART MOBILE PHONES BY ELEMENTARY SCHOOL STUDENTS

Trends in Education, 2023-01, Vol.15 (1)

2023

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Torsion of the spleen--an unusual cause of sudden acute abdomen

Rozhledy v chirurgii, 2002-09, Vol.81 (9), p.492

2002

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DNA methylation and neoplasms

Časopis lékařů českých, 2000-05, Vol.139 (10), p.291

2000

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Subtypes of autism by cluster analysis based on structural MRI data

European child & adolescent psychiatry, 2005-06, Vol.14 (3), p.138-144

2005

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Diagnosis of spontaneous arteriovenous fistula complicating aortoiliac aneurysm using spiral CT. Report of 3 cases

Rozhledy v chirurgii, 2004-10, Vol.83 (10), p.493

2004

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Neolitická osada v Ohrade u Kolína

Archeologické rozhledy (Praha), 1994-01, Vol.46 (3), p.410-428

1994

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Genetic study of 20 patients with autism disorders

Časopis lékařů českých, 2002-06, Vol.141 (12), p.381

2002

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Use of DNA analysis in medicine

Časopis lékařů českých, 1992-06, Vol.131 (12), p.357

1992

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The experience with the foetal diagnosis of the cystic fibrosis in the second and first trimester

Acta Universitatis Carolinae. Medica, 1990, Vol.36 (1-4), p.120

1990

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Tumor suppressor genes

Časopis lékařů českých, 1997-01, Vol.136 (1), p.11

1997

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The rapid molecular genetic diagnosis of cystic fibrosis by polymerase chain reaction: an experience report

Czechoslovak medicine, 1990, Vol.13 (4), p.145

1990

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A rare cause of mediastinal expansion with a massive pleural effusion

The expression of PAX5, p53 immunohistochemistry and p53 mutation analysis in superficial bladder carcinoma tissue. Correlation with pathological findings and clinical outcome

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains

The human genome and medicine

Non-linear free streaming in Vlasov plasma

A database of germline p53 mutations in cancer-prone families

Oncogene amplification and expression in pediatric solid tumors

When is it useful to look for TP53 germline gene mutations in families of oncology patients?

Two Li-Fraumeni syndrome families with novel germline p53 mutations : loss of the wild-type p53 allele in only 50% of tumours

The amphioxus rab GDP-dissociation inhibitor (GDI) gene is neural-specific: implications for the evolution of chordate rab GDI genes

The human genome--chromosome X. Focus on Xq28

Genetics of autism

Not EEG abnormalities but epilepsy is associated with autistic regression and mental functioning in childhood autism

Stationary equilibria of a collisionless plasma treated by the moment method

SECURITY QUESTIONS OF THE USE OF SMART MOBILE PHONES BY ELEMENTARY SCHOOL STUDENTS

Torsion of the spleen--an unusual cause of sudden acute abdomen

DNA methylation and neoplasms

Subtypes of autism by cluster analysis based on structural MRI data

Diagnosis of spontaneous arteriovenous fistula complicating aortoiliac aneurysm using spiral CT. Report of 3 cases

Neolitická osada v Ohrade u Kolína

Genetic study of 20 patients with autism disorders

Use of DNA analysis in medicine

The experience with the foetal diagnosis of the cystic fibrosis in the second and first trimester

Tumor suppressor genes

The rapid molecular genetic diagnosis of cystic fibrosis by polymerase chain reaction: an experience report

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