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Year Number of Results
2004 1
2007 1
2008 2
2009 2
2011 2
2012 3
2013 3
2015 2
2016 4
2017 2
2018 3
2019 4
2020 1
2021 3
2022 10
2023 3
2024 1

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41 results

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Page 1
Reply to: Questioning the cycad theory of Kii ALS-PDC causation.
Menšíková K, Rosales R, Colosimo C, Spencer P, Lannuzel A, Ugawa Y, Sasaki R, Giménez-Roldán S, Matej R, Tuckova L, Hrabos D, Kolarikova K, Vodicka R, Vrtel R, Strnad M, Hlustik P, Otruba P, Prochazka M, Bares M, Boluda S, Buee L, Ransmayr G, Kaňovský P. Menšíková K, et al. Among authors: vrtel r. Nat Rev Neurol. 2024 Mar;20(3):195-196. doi: 10.1038/s41582-024-00938-y. Nat Rev Neurol. 2024. PMID: 38336911 No abstract available.
Endemic parkinsonism: clusters, biology and clinical features.
Menšíková K, Steele JC, Rosales R, Colosimo C, Spencer P, Lannuzel A, Ugawa Y, Sasaki R, Giménez-Roldán S, Matej R, Tuckova L, Hrabos D, Kolarikova K, Vodicka R, Vrtel R, Strnad M, Hlustik P, Otruba P, Prochazka M, Bares M, Boluda S, Buee L, Ransmayr G, Kaňovský P. Menšíková K, et al. Among authors: vrtel r. Nat Rev Neurol. 2023 Oct;19(10):599-616. doi: 10.1038/s41582-023-00866-3. Epub 2023 Sep 8. Nat Rev Neurol. 2023. PMID: 37684518 Review.
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk.
Stolarova L, Kleiblova P, Zemankova P, Stastna B, Janatova M, Soukupova J, Achatz MI, Ambrosone C, Apostolou P, Arun BK, Auer P, Barnard M, Bertelsen B; Biobank Japan; Blok MJ, Boddicker N, Brunet J, Burnside ES, Calvello M, Campbell I, Chan SH, Chen F, Chiang JB, Coppa A, Cortesi L, Crujeiras-González A; Consortium CZECANCA; De Leeneer K, De Putter R, DePersia A, Devereux L, Domchek S, Efremidis A, Engel C, Ernst C, Evans DGR, Feliubadaló L, Fostira F, Fuentes-Ríos O, Gómez-García EB, González S, Haiman C, Hansen TVO, Hauke J, Hodge J, Hu C, Huang H, Ishak NDB, Iwasaki Y, Konstantopoulou I, Kraft P, Lacey J, Lázaro C, Li N, Lim WK, Lindstrom S, Lori A, Martinez E, Martins A, Matsuda K, Matullo G, McInerny S, Michailidou K, Montagna M, Monteiro ANA, Mori L, Nathanson K, Neuhausen SL, Nevanlinna H, Olson JE, Palmer J, Pasini B, Patel A, Piane M, Poppe B, Radice P, Renieri A, Resta N, Richardson ME, Rosseel T, Ruddy KJ, Santamariña M, Dos Santos ES, Teras L, Toland AE, Trentham-Dietz A, Vachon CM, Volk AE, Weber-Lassalle N, Weitzel JN, Wiesmuller L, Winham S, Yadav S, Yannoukakos D, Yao S, Zampiga V, Zethoven M, Zhang ZW, Zima T, Spurdle AB, Vega A, Rossing M, Del Valle J, De Nicolo… See abstract for full author list ➔ Stolarova L, et al. Clin Cancer Res. 2023 Aug 15;29(16):3037-3050. doi: 10.1158/1078-0432.CCR-23-0212. Clin Cancer Res. 2023. PMID: 37449874 Free PMC article.
Prenatal detection of copy number variants in fetuses with detected congenital devolpmental disordes, from 2015 to 2020 by Multiplex Ligation-Dependent Probe Amplification and microarray analysis.
Štefeková Andrea, Čapková Pavlína, Curtisová Václava, Mracká Enghjargalan, Filipová Hana, Spurná Zuzana, Procházka Martin, Ľubušký Marek, Pilka Radovan, Vrtěl Radek. Štefeková Andrea, et al. Among authors: vrtel radek. Ceska Gynekol. 2023;88(3):162-171. doi: 10.48095/cccg2023162. Ceska Gynekol. 2023. PMID: 37344181 English.
Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features.
Pavlicek J, Soucek O, Vrtel R, Klaskova E, Hana V, Stara V, Adamova K, Fürst T, Hana V Jr, Kapralova S, Prochazka M, Snajderova M, Tomaskova H, Tüdös Z, Vrbicka D, Vrtel P, Zapletalova J, Tauber Z, Lebl J. Pavlicek J, et al. Among authors: vrtel r. Horm Res Paediatr. 2022;95(5):465-475. doi: 10.1159/000525823. Epub 2022 Jul 1. Horm Res Paediatr. 2022. PMID: 35970147
Ovarian tumors and genetic predisposition.
Štellmachová Júlia, Vrtěl Petr, Vrtěl Radek, Janíková Mária, Kolaříková Kristýna, Procházka Martin, Vodička Radek. Štellmachová Júlia, et al. Among authors: vrtel radek. Ceska Gynekol. 2022;87(3):211-216. doi: 10.48095/cccg2022211. Ceska Gynekol. 2022. PMID: 35896402 English.
Screening for congenital defects and genetic diseases of the fetus at University Hospital in Olomouc and sending/ reporting to the National register of reproductive health in the Czech Republic.
Maděrková Tozzi Michaela, Dvořák Jr. Vladimír, Klásková Eva, Šuláková Soňa, Wita Martin, Hálek Jan, Vrtěl Radek, Curtisová Václava, Pilka Radovan, Dušek Ladislav, Ľubušký Marek. Maděrková Tozzi Michaela, et al. Among authors: vrtel radek. Ceska Gynekol. 2022;87(3):162-172. doi: 10.48095/cccg2022162. Ceska Gynekol. 2022. PMID: 35896393 English.
Reply: Matters Arising 'Lewy body disease or diseases with Lewy bodies?'.
Menšíková K, Matěj R, Colosimo C, Rosales R, Tučková L, Ehrmann J, Hraboš D, Kolaříková K, Vodička R, Vrtěl R, Procházka M, Nevrlý M, Kaiserová M, Kurčová S, Otruba P, Kaňovský P. Menšíková K, et al. Among authors: vrtel r. NPJ Parkinsons Dis. 2022 Jun 23;8(1):80. doi: 10.1038/s41531-022-00338-3. NPJ Parkinsons Dis. 2022. PMID: 35739112 Free PMC article. No abstract available.
Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing.
Vrtel P, Slavik L, Vodicka R, Stellmachova J, Prochazka M, Prochazkova J, Ulehlova J, Rohon P, Simurda T, Stasko J, Martinkova I, Vrtel R. Vrtel P, et al. Among authors: vrtel r. Diagnostics (Basel). 2022 Apr 23;12(5):1060. doi: 10.3390/diagnostics12051060. Diagnostics (Basel). 2022. PMID: 35626216 Free PMC article.
41 results