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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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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, 374-371

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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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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Multiple Unilateral Reddish Tumors on the Ear and Forehead in a Woman With Early Syphilis

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

Filo, Viliam

1994

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

2012

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Favorable Long Term Outcome of Locally Advanced Adenocarcinoma Epididymis - An Extended Follow-Up: Case Report

Mathews Journal of Case Reports, 2023-01, Vol.8 (1)

2023

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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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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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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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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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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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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.578-592

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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Novel mutations in the homogentisate- 1,2-dioxygenase gene identified in Slovak patients with alkaptonuria

Journal of medical genetics, 2000-07, Vol.37 (7), p.539-542

ZATKOVA, A

2000

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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

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

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

Multiple Unilateral Reddish Tumors on the Ear and Forehead in a Woman With Early Syphilis

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

Favorable Long Term Outcome of Locally Advanced Adenocarcinoma Epididymis - An Extended Follow-Up: 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

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

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

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

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

Novel mutations in the homogentisate- 1,2-dioxygenase gene identified in Slovak patients with alkaptonuria

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