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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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Spindle cell and cuboidal renal cell carcinoma (loopoma). 10 case reports

Časopis lékařů českých, 2004, Vol.143 (3), p.169

2004

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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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Studdy on arteriovenous malformmation at the carotid-vertebral artery anastomosis

Bratislavské lékarské listy, 1973, Vol.60 (5), p.622

1973

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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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Association of antral, Jejuno-ileal atresias and biliary peritonitis : an unusual case

Indian journal of pediatrics, 1992-05, Vol.59 (3), p.380-383

1992

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Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

Journal of medical genetics, 1999-04, Vol.36 (4), p.290-294

1999

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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, 2012-02, Vol.35 (1-2), p.43-45

2012

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The Western and Eastern Roots of the Saami—the Story of Genetic “Outliers” Told by Mitochondrial DNA and Y Chromosomes

American journal of human genetics, 2004-04, Vol.74 (4), p.661-682

2004

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High Frequency of Alkaptonuria in Slovakia: Evidence for the Appearance of Multiple Mutations in HGO Involving Different Mutational Hot Spots

American journal of human genetics, 2000-11, Vol.67 (5), p.1333-1339

2000

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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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Deep common ancestry of Indian and western-Eurasian mitochondrial DNA lineages

Current biology, 1999-11, Vol.9 (22), p.1331-1334

1999

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Correlation between Genotype and Phenotype in Patients with Cystic Fibrosis

The New England journal of medicine, 1993-10, Vol.329 (18), p.1308-1313

1993

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Linkage of Autosomal Recessive Primary Congenital Glaucoma to the GLC3A Locus in Roms (Gypsies) from Slovakia

Human heredity, 1998-01, Vol.48 (1), p.30-33

1998

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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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Lactase Haplotype Diversity in the Old World

American journal of human genetics, 2001-01, Vol.68 (1), p.160-172

2001

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Reconstructing the Population History of European Romani from Genome-wide Data

Current biology, 2012-12, Vol.22 (24), p.2342-2349

2012

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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

Spindle cell and cuboidal renal cell carcinoma (loopoma). 10 case reports

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

Studdy on arteriovenous malformmation at the carotid-vertebral artery anastomosis

Traumatic aneurysm of a cerebral artery

Spontaneous subarachnoid hemorrhage in ependymoma

Association of antral, Jejuno-ileal atresias and biliary peritonitis : an unusual case

Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

Population genetic data for 16 STR loci in Slovakia

Radiotherapy in the treatment of epididymal adenocarcinoma - case report

The Western and Eastern Roots of the Saami—the Story of Genetic “Outliers” Told by Mitochondrial DNA and Y Chromosomes

High Frequency of Alkaptonuria in Slovakia: Evidence for the Appearance of Multiple Mutations in HGO Involving Different Mutational Hot Spots

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

Deep common ancestry of Indian and western-Eurasian mitochondrial DNA lineages

Correlation between Genotype and Phenotype in Patients with Cystic Fibrosis

Linkage of Autosomal Recessive Primary Congenital Glaucoma to the GLC3A Locus in Roms (Gypsies) from Slovakia

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

Lactase Haplotype Diversity in the Old World

Reconstructing the Population History of European Romani from Genome-wide Data

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