Familial hematuria: A review von Plevová, Pavlína, Gut, Josef, Janda, Jan

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An Update on Inherited Colon Cancer and Gastrointestinal Polyposis von Plevová, Pavlína

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Genetic Causes of Rare Pediatric Ovarian Tumors von Plevová, Pavlína, Geržová, Hedvika

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Four novel point mutations in the PMP22 gene with phenotypes of HNPP and Dejerine-Sottas neuropathy von Brožková, Dana, Mazanec, Radim, Rychlý, Zdeněk, Haberlová, Jana, Böhm, Jiří, Staněk, Jan, Plevová, Pavlína, Lisoňová, Jana, Sabová, Jana, Sakmaryová, Iva, Seeman, Pavel

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Expression of the hMLH1 and hMSH2 proteins in normal tissues: relationship to cancer predisposition in hereditary non-polyposis colon cancer von PLEVOVA, Pavlina, SEDLAKOVA, Eva, ZAPLETALOVA, Jana, KREPELOVA, Anna, SKYPALOVA, Petra, KOLAR, Zdenek

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Elejalde syndrome—A case report von SIHANOVA, Eva, PLEVOVA, Pavlina, CURIK, Romuald, KASPERCIK, Ivo, KREPELOVA, Anna

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Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria von Savige, Judy, Storey, Helen, Watson, Elizabeth, Hertz, Jens Michael, Deltas, Constantinos, Renieri, Alessandra, Mari, Francesca, Hilbert, Pascale, Plevova, Pavlina, Byers, Peter, Cerkauskaite, Agne, Gregory, Martin, Cerkauskiene, Rimante, Ljubanovic, Danica Galesic, Becherucci, Francesca, Errichiello, Carmela, Massella, Laura, Aiello, Valeria, Lennon, Rachel, Hopkinson, Louise, Koziell, Ania, Lungu, Adrian, Rothe, Hansjorg Martin, Hoefele, Julia, Zacchia, Miriam, Martic, Tamara Nikuseva, Gupta, Asheeta, van Eerde, Albertien, Gear, Susie, Landini, Samuela, Palazzo, Viviana, Al-Rabadi, Laith, Claes, Kathleen, Corveleyn, Anniek, Van Hoof, Evelien, van Geel, Micheel, Williams, Maggie, Ashton, Emma, Belge, Hendica, Ars, Elisabeth, Bierzynska, Agnieszka, Gangemi, Concetta, Lipska-Ziętkiewicz, Beata S

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The APOE ε2 allele is associated with increased plasma apolipoprotein E levels in patients with coronary artery disease von Pleva, Leoš, Kušnierová, Pavlína, Plevová, Pavlína, Hilscherová, Šárka, Karpíšek, Michal, Zapletalová, Jana, Faldynová, Lucie, Kovářová, Petra, Kukla, Pavel

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STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic von Plevova, Pavlina, Paprskarova, Martina, Tvrda, Petra, Turska, Petra, Slavkovsky, Rastislav, Mrazkova, Eva

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Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene von Čada, Zdeněk, Šafka Brožková, Dana, Balatková, Zuzana, Plevová, Pavlína, Rašková, Dagmar, Laštůvková, Jana, Černý, Rudolf, Bandúrová, Veronika, Koucký, Vladimír, Hrubá, Silvie, Komarc, Martin, Jenčík, Ján, Poisson Marková, Simona, Plzák, Jan, Kluh, Jan, Seeman, Pavel

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Familiar Mediterranean fever in Czech Republic von Sedivá, Anna, Maňásek, Viktor, Gřegořová, Andrea, Plevová, Pavlína, Toplak, Nataša, Debeljak, Maruša

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Breast cancer in monozygotic twins von Hladíková, A, Plevová, P, Macháčková, E

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Increased levels of MMP-3, MMP-9 and MPO represent predictors of in-stent restenosis, while increased levels of ADMA, LCAT, ApoE and ApoD predict bare metal stent patency von Pleva, Leos, Kusnierova, Pavlina, Plevova, Pavlina, Zapletalova, Jana, Karpisek, Michal, Faldynova, Lucie, Kovarova, Petra, Kukla, Pavel

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A founder COL4A4 pathogenic variant resulting in autosomal recessive Alport syndrome accounts for most genetic kidney failure in Romani people von Plevova, Pavlina, Indrakova, Jana, Savige, Judy, Kuhnova, Petra, Tvrda, Petra, Cerna, Dita, Hilscherova, Sarka, Kudrejova, Monika, Polendova, Daniela, Jaklova, Radka, Langova, Martina, Jahnova, Helena, Lastuvkova, Jana, Dusek, Jiri, Gut, Josef, Vlckova, Marketa, Solarova, Pavla, Kreckova, Gabriela, Kantorova, Eva, Soukalova, Jana, Slavkovsky, Rastislav, Zapletalova, Jana, Tichy, Tomas, Thomasova, Dana

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Guidelines for Genetic Testing and Management of Alport Syndrome von Savige, Judy, Lipska-Zietkiewicz, Beata S, Watson, Elizabeth, Hertz, Jens Michael, Deltas, Constantinos, Mari, Francesca, Hilbert, Pascale, Plevova, Pavlina, Byers, Peter, Cerkauskaite, Agne, Gregory, Martin, Cerkauskiene, Rimante, Ljubanovic, Danica Galesic, Becherucci, Francesca, Errichiello, Carmela, Massella, Laura, Aiello, Valeria, Lennon, Rachel, Hopkinson, Louise, Koziell, Ania, Lungu, Adrian, Rothe, Hansjorg Martin, Hoefele, Julia, Zacchia, Miriam, Martic, Tamara Nikuseva, Gupta, Asheeta, van Eerde, Albertien, Gear, Susie, Landini, Samuela, Palazzo, Viviana, Al-Rabadi, Laith, Claes, Kathleen, Corveleyn, Anniek, Van Hoof, Evelien, van Geel, Micheel, Williams, Maggie, Ashton, Emma, Belge, Hendica, Ars, Elisabet, Bierzynska, Agnieszka, Gangemi, Concetta, Renieri, Alessandra, Storey, Helen, Flinter, Frances

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Epidermal growth factor receptor expression in colorectal tumors with and without microsatellite instability von Plevová, Pavlína, Sedláková, Eva, Papezová, Martina, Zapletalová, Jana, Curik, Romuald, Kolár, Zdenek, Krepelová, Anna

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HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain von Jolly, Lachlan A, Nguyen, Lam Son, Domingo, Deepti, Sun, Ying, Barry, Simon, Hancarova, Miroslava, Plevova, Pavlina, Vlckova, Marketa, Havlovicova, Marketa, Kalscheuer, Vera M, Graziano, Claudio, Pippucci, Tommaso, Bonora, Elena, Sedlacek, Zdenek, Gecz, Jozef

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Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria von Savige, Judy, Storey, Helen, Watson, Elizabeth, Hertz, Jens Michael, Deltas, Constantinos, Renieri, Alessandra, Mari, Francesca, Hilbert, Pascale, Plevova, Pavlina, Byers, Peter, Cerkauskaite, Agne, Gregory, Martin, Cerkauskiene, Rimante, Ljubanovic, Danica Galesic, Becherucci, Francesca, Errichiello, Carmela, Massella, Laura, Aiello, Valeria, Lennon, Rachel, Hopkinson, Louise, Koziell, Ania, Lungu, Adrian, Rothe, Hansjorg Martin, Hoefele, Julia, Zacchia, Miriam, Martic, Tamara Nikuseva, Gupta, Asheeta, van Eerde, Albertien, Gear, Susie, Landini, Samuela, Palazzo, Viviana, Al-Rabadi, Laith, Claes, Kathleen, Corveleyn, Anniek, Van Hoof, Evelien, van Geel, Micheel, Williams, Maggie, Ashton, Emma, Belge, Hendica, Ars, Elisabeth, Bierzynska, Agnieszka, Gangemi, Concetta, Lipska-Ziętkiewicz, Beata S

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Guidelines for Genetic Testing and Management of Alport Syndrome von Savige, Judy, Lipska-Zietkiewicz, Beata S, Watson, Elizabeth, Hertz, Jens Michael, Deltas, Constantinos, Mari, Francesca, Hilbert, Pascale, Plevova, Pavlina, Byers, Peter, Cerkauskaite, Agne, Gregory, Martin, Cerkauskiene, Rimante, Ljubanovic, Danica Galesic, Becherucci, Francesca, Errichiello, Carmela, Massella, Laura, Aiello, Valeria, Lennon, Rachel, Hopkinson, Louise, Koziell, Ania, Lungu, Adrian, Rothe, Hansjorg Martin, Hoefele, Julia, Zacchia, Miriam, Martic, Tamara Nikuseva, Gupta, Asheeta, van Eerde, Albertien, Gear, Susie, Landini, Samuela, Palazzo, Viviana, al-Rabadi, Laith, Claes, Kathleen, Corveleyn, Anniek, Van Hoof, Evelien, van Geel, Micheel, Williams, Maggie, Ashton, Emma, Belge, Hendica, Ars, Elisabet, Bierzynska, Agnieszka, Gangemi, Concetta, Renieri, Alessandra, Storey, Helen, Flinter, Frances

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Dědičné nádorové syndromy s možnou manifestací prenatálně von Plevová, Pavlína, Grečmalová, Dagmar

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