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Spindle and cuboidal renal cell carcinoma, a tumour having frequent association with nephrolithiasis: report of 11 cases including a case with hybrid conventional renal cell carcinoma/ spindle and cuboidal renal cell carcinoma components

Histopathology, 2002-12, Vol.41 (6), p.549-555

2002

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Intususception of appendical cystadenoma imitating a caecal tumor

Rozhledy v chirurgii, 2005-12, Vol.84 (12), p.617

2005

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Appendectomy--comparison of results of laparoscopy versus open surgery

Rozhledy v chirurgii, 2007-02, Vol.86 (2), p.92

2007

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The Peutz-Jeghers syndrome--a case review

Rozhledy v chirurgii, 2007-01, Vol.86 (1), p.24

2007

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Multiple unilateral reddish tumors on the ear and forehead in a woman with early syphilis. Angiolymphoid hyperplasia (ALHE) with eosinophilia coexisting with early latent syphilis

Archives of dermatology (1960), 1994-03, Vol.130 (3), p.371, 374

1994

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The etiology of underlying liver lesions in 70 autopsied cases of hepatocellular carcinoma

Neoplasma, 1985, Vol.32 (5), p.629

1985

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Traumatic aneurysm of a cerebral artery

Ceskoslovenska neurologie a neurochirurgie, 1983-09, Vol.46 (5), p.336

1983

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Spontaneous subarachnoid hemorrhage in ependymoma

Ceskoslovenska neurologie a neurochirurgie, 1981-07, Vol.44 (4), p.230

1981

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Population genetic data for 16 STR loci in Slovakia

Legal medicine (Tokyo, Japan), 2018-09, Vol.34, p.36-40

2018

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Radiotherapy in the treatment of epididymal adenocarcinoma - case report

Onkologie, 2012, Vol.35 (1-2), p.43-45

2012

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High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL)

General physiology and biophysics, 2003-12, Vol.22 (4), p.549

2003

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Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia

General physiology and biophysics, 2007-12, Vol.26 (4), p.306-310

2007

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Expanding the morphologic spectrum of chromophobe renal cell carcinoma: A study of 8 cases with papillary architecture

Annals of diagnostic pathology, 2020-02, Vol.44, p.151448-151448, Article 151448

2020

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A Clinicopathological Study of 29 Spitzoid Melanocytic Lesions With ALK Fusions, Including Novel Fusion Variants, Accompanied by Fluorescence In Situ Hybridization Analysis for Chromosomal Copy Number Changes, and Both TERT Promoter and Next-Generation Sequencing Mutation Analysis

The American journal of dermatopathology, 2020-08, Vol.42 (8), p.578

2020

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Papillary renal cell carcinoma with prominent spindle cell stroma - tumor mimicking mixed epithelial and stromal tumor of the kidney: Clinicopathologic, morphologic, immunohistochemical and molecular genetic analysis of 6 cases

Annals of diagnostic pathology, 2020-02, Vol.44, p.151441-151441, Article 151441

2020

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2 clinico-genetic types of primary congenital glaucomas in Slovakia

Česká a slovenská oftalmologie, 1998, Vol.54 (5), p.289

1998

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Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma

Česká a slovenská oftalmologie, 1998, Vol.54 (5), p.281

1998

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PKU in Slovakia : mutation screening and haplotype analysis

Human genetics, 1995, Vol.95 (1), p.112-114

1995

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Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset

Human genetics, 1982, Vol.61 (3), p.193-197

1982

Volltextzugriff (PDF)

P3-347 Frontotemporal dementia with spastic quadruparesis with intronic polymorfism of tau protein's gene — a case report

Neurobiology of aging, 2004-07, Vol.25, p.S454-S454

2004

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Deletion ΔF508 and haplotype analysis of CFTR gene region in Slovak CF patients

Human genetics, 1992-05, Vol.89 (3), p.305-306

1992

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The Dermatoglyphics of Egyptian Nubians

Trends in Dermatoglyphic Research, p.234-243

Volltextzugriff (PDF)

Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effect

Human genetics, 1982-10, Vol.61 (3), p.198-200

1982

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Haplotype analysis of the CFTR gene region and the proportion of delta F508 deletion in Slovak patients with cystic fibrosis

Functional and developmental morphology, 1992, Vol.2 (2), p.141

1992

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A unique RFLP haplotype at the phenylalanine hydroxylase locus in Czechoslovak Gypsies with phenylketonuria

Functional and developmental morphology, 1992, Vol.2 (2), p.139

1992

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Spindle and cuboidal renal cell carcinoma, a tumour having frequent association with nephrolithiasis: report of 11 cases including a case with hybrid conventional renal cell carcinoma/ spindle and cuboidal renal cell carcinoma components

Intususception of appendical cystadenoma imitating a caecal tumor

Appendectomy--comparison of results of laparoscopy versus open surgery

The Peutz-Jeghers syndrome--a case review

Multiple unilateral reddish tumors on the ear and forehead in a woman with early syphilis. Angiolymphoid hyperplasia (ALHE) with eosinophilia coexisting with early latent syphilis

The etiology of underlying liver lesions in 70 autopsied cases of hepatocellular carcinoma

Traumatic aneurysm of a cerebral artery

Spontaneous subarachnoid hemorrhage in ependymoma

Population genetic data for 16 STR loci in Slovakia

Radiotherapy in the treatment of epididymal adenocarcinoma - case report

High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL)

Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia

Expanding the morphologic spectrum of chromophobe renal cell carcinoma: A study of 8 cases with papillary architecture

A Clinicopathological Study of 29 Spitzoid Melanocytic Lesions With ALK Fusions, Including Novel Fusion Variants, Accompanied by Fluorescence In Situ Hybridization Analysis for Chromosomal Copy Number Changes, and Both TERT Promoter and Next-Generation Sequencing Mutation Analysis

Papillary renal cell carcinoma with prominent spindle cell stroma - tumor mimicking mixed epithelial and stromal tumor of the kidney: Clinicopathologic, morphologic, immunohistochemical and molecular genetic analysis of 6 cases

2 clinico-genetic types of primary congenital glaucomas in Slovakia

Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma

PKU in Slovakia : mutation screening and haplotype analysis

Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset

P3-347 Frontotemporal dementia with spastic quadruparesis with intronic polymorfism of tau protein's gene — a case report

Deletion ΔF508 and haplotype analysis of CFTR gene region in Slovak CF patients

The Dermatoglyphics of Egyptian Nubians

Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effect

Haplotype analysis of the CFTR gene region and the proportion of delta F508 deletion in Slovak patients with cystic fibrosis

A unique RFLP haplotype at the phenylalanine hydroxylase locus in Czechoslovak Gypsies with phenylketonuria

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