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Minimal residual disease detection using real-time quantitative PCR analysis of immunoglobulin and T-cell receptor gene rearrangements in the non-MRD-based ALL IC-BFM 2002 protocol for childhood ALL: Slovak experience.
Kolenova A, Hikkel I, Ilencikova D, Hikkelova M, Sejnova D, Kaiserova E, Cizmar A, Puskacova J, Bubanska E, Oravkinova I, Gencik M. Kolenova A, et al. Among authors: hikkelova m. Neoplasma. 2010;57(6):552-61. doi: 10.4149/neo_2010_06_552. Neoplasma. 2010. PMID: 20845994
Novel missense variant of CACNA1A gene in a Slovak family with episodic ataxia type 2.
Petrovicova A, Brozman M, Kurca E, Gobo T, Dluha J, Kalmarova K, Nosal V, Hikkelova M, Krajciova A, Burjanivova T, Sivak S. Petrovicova A, et al. Among authors: hikkelova m. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2017 Mar;161(1):107-110. doi: 10.5507/bp.2016.066. Epub 2017 Jan 13. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2017. PMID: 28096552 Free article.
Novel missense variant of CACNA1A gene: A case report of a family with episodic ataxia type 2.
Sivák Š, Kurča E, Krajčiová A, Hikkelová M, Šimko J, Mišovicová N, Kantorová E, Turčanová-Koprušáková M, Burjanivová T, Čierny D, Nosál' V. Sivák Š, et al. Among authors: hikkelova m. J Neurol Sci. 2017 May 15;376:119-120. doi: 10.1016/j.jns.2017.03.008. Epub 2017 Mar 11. J Neurol Sci. 2017. PMID: 28431595 No abstract available.
Brain of miyoshi myopathy/dysferlinopathy patients presents with structural and metabolic anomalies.
Hnilicova P, Grendar M, Turcanova Koprusakova M, Trancikova Kralova A, Harsanyiova J, Krssak M, Just I, Misovicova N, Hikkelova M, Grossmann J, Spalek P, Meciarova I, Kurca E, Zilka N, Zelenak K, Bogner W, Kolisek M. Hnilicova P, et al. Among authors: hikkelova m. Sci Rep. 2024 Aug 20;14(1):19267. doi: 10.1038/s41598-024-69966-4. Sci Rep. 2024. PMID: 39164335 Free PMC article.