About: Kristýna Pivovarčíková

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
field of work	wds:Q56924456-6DAA787D-0EC1-46D9-9AD5-F70604954D6C wds:Q56924456-CABCCCAB-8E0C-43B0-B899-DBB0244F452C
field of work	medicine pathology
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) patoložka (cs) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідниця (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtuese (sq)
rdfs:label	Kristyna Pivovarcikova (es) Kristyna Pivovarcikova (nl) Kristyna Pivovarcikova (ast) Kristýna Pivovarčíková (cs) Kristýna Pivovarčíková (en)
skos:prefLabel	Kristyna Pivovarcikova (es) Kristyna Pivovarcikova (nl) Kristyna Pivovarcikova (ast) Kristýna Pivovarčíková (cs) Kristýna Pivovarčíková (en)
name	Kristyna Pivovarcikova (es) Kristyna Pivovarcikova (nl) Kristyna Pivovarcikova (ast) Kristýna Pivovarčíková (cs) Kristýna Pivovarčíková (en)
Scopus author ID	wds:Q56924456-BBC7BD28-1ECF-4B05-9645-A4A769899D86
Scopus author ID	56003922800
given name	wds:Q56924456-DB7EC48D-851E-480E-B8C8-217B3DB3B764
given name	Kristýna
described by source	wds:Q56924456-40AC8227-1211-4353-A729-50981BB722E8
instance of	wds:Q56924456-BD4AF867-6D93-44B7-B25B-4916353C0BFC
NL CR AUT ID	wds:Q56924456-12707191-4c63-3836-7a1b-ba300df5516f
described by source	Medvik
instance of	Homo sapiens
NL CR AUT ID	xx0233028
occupation	wds:Q56924456-52BD6FD1-CE5B-42C7-ABEE-2085373920CF wds:Q56924456-5A5AF60C-503D-47D2-8A81-F76F52B9D444 wds:Q56924456-f4734fd2-d368-4f04-922c-69733cda97dc
employer	wds:Q56924456-D9BF4239-71CB-42B5-839C-89BCFB46560C wds:Q56924456-DB00E47B-1437-4589-ACE4-AA70F55BC1E9
languages spoken, written or signed	wds:Q56924456-45A3CDC4-D3EF-45D4-8B9E-ED6D24D29486
sex or gender	wds:Q56924456-C8F8FD43-E3C1-4315-BB00-FC9A597B7D39
VIAF ID	wds:Q56924456-6F20943B-8B33-4EBA-803A-22FF626FCA53
WorldCat Identities ID (superseded)	wds:Q56924456-4E3DA901-981C-46BA-AEFB-CAB41FEF7ECF
VIAF ID	http://viaf.org/viaf/25155190006882132414
occupation	pathologist physician researcher
employer	Charles University Faculty of Medicine in Pilsen, Charles University
languages spoken, written or signed	Czech
sex or gender	female organism
VIAF ID	25155190006882132414
WorldCat Identities ID (superseded)	viaf-25155190006882132414
ORCID iD	wds:Q56924456-DF48A556-7AEA-43DB-A37B-55C13E4E5548
Dimensions author ID	wds:Q56924456-752B4252-2E8B-4D50-9FBD-DF52EC233B95
ORCID iD	https://orcid.org/0000-0002-9553-0105
ORCID iD	0000-0002-9553-0105
Dimensions author ID	01172207766.37
ResearcherID	wds:Q56924456-54946064-C68F-427D-9670-22D5019D9E04
ResearcherID	Q-5634-2018
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56924456
is author of	Solid papillary renal cell carcinoma: clinicopathologic, morphologic, and immunohistochemical analysis of 10 cases and review of the literature Chromophobe renal cell carcinoma with neuroendocrine and neuroendocrine-like features. Morphologic, immunohistochemical, ultrastructural, and array comparative genomic hybridization analysis of 18 cases and review of the literature Biphasic Squamoid Alveolar Renal Cell Carcinoma: A Distinctive Subtype of Papillary Renal Cell Carcinoma? Advances in Experimental Targeted Therapy and Immunotherapy for Patients with Glioblastoma Multiforme. Aggressive and nonaggressive translocation t(6;11) renal cell carcinoma: comparative study of 6 cases and review of the literature Low-grade Spindle Cell Proliferation in Clear Cell Renal Cell Carcinoma is Unlikely to be an Initial Step in Sarcomatoid Differentiation. Papillary renal cell carcinoma with cytologic and molecular genetic features overlapping with renal oncocytoma: Analysis of 10 cases Mucinous spindle and tubular renal cell carcinoma: analysis of chromosomal aberration pattern of low-grade, high-grade, and overlapping morphologic variant with papillary renal cell carcinoma. Renal Cell Carcinoma With Leiomyomatous Stroma: A Group of Tumors With Indistinguishable Histopathologic Features, But 2 Distinct Genetic Profiles: Next-Generation Sequencing Analysis of 6 Cases Negative for Aberrations Related to the VHL gene Warthin-like papillary renal cell carcinoma: Clinicopathologic, morphologic, immunohistochemical and molecular genetic analysis of 11 cases Cystic and necrotic papillary renal cell carcinoma: prognosis, morphology, immunohistochemical, and molecular-genetic profile of 10 cases Molecular-genetic analysis is essential for accurate classification of renal carcinoma resembling Xp11.2 translocation carcinoma. TFE3-Fusion Variant Analysis Defines Specific Clinicopathologic Associations Amog Xp11 Translocation Cancers Renal cell carcinoma with leiomyomatous stroma--further immunohistochemical and molecular genetic characteristics of unusual entity Foamy cell (hibernoma-like) change is a rare histopathological feature in renal cell carcinoma Comparative study of TERT gene mutation analysis on voided liquid-based urine cytology and paraffin-embedded tumorous tissue. Magnetic resonance imaging as an adjunct diagnostic tool in computed tomography defined Bosniak IIF-III renal cysts: a multicenter study. Distinctive renal cell tumor simulating atrophic kidney with 2 types of microcalcifications. Report of 3 cases. The leiomyomatous stroma in renal cell carcinomas is polyclonal and not part of the neoplastic process. Choriogonadotropin positive seminoma-a clinicopathological and molecular genetic study of 15 cases Programmed death-1 (PD-1) receptor/PD-1 ligand (PD-L1) expression in fumarate hydratase-deficient renal cell carcinoma. "Mucin"-secreting papillary renal cell carcinoma: clinicopathological, immunohistochemical, and molecular genetic analysis of seven cases. Morphological, immunohistochemical, and chromosomal analysis of multicystic chromophobe renal cell carcinoma, an architecturally unusual challenging variant. High-grade renal cell carcinoma with emperipolesis: Clinicopathological, immunohistochemical and molecular-genetic analysis of 14 cases. Mixed Epithelial and Stromal Tumor of the Kidney: Mutation Analysis of the DICER 1 Gene in 29 Cases.
is author of	wds:Q38840969-83E3576E-32A0-4CB4-82F6-AF8AA82A064C wds:Q38510998-3089C8BD-D6B6-41B6-820B-7E099DB384C6 wds:Q39901657-5F927270-C7C1-454B-9FB8-892FAB296ACB wds:Q47384466-20ED6619-BD1A-4828-8AD1-7495B5D20A59

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