Katalóg evidencie publikačnej činnosti PU

ID záznamu:	PU.Prešov.2011031611311596
Kategória:	ADC
Autor:	Dojčáková Dana (80%)
Autor:	Frykholm C. (5%)
Autor:	Friberg U. (3%)
Autor:	Lahsaee S. (3%)
Autor:	Entesarian M. (3%)
Autor:	Dahl N. (3%)
Autor:	Klar J. (3%)
Názov:	Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association [print, elektronický dokument]
Zdroj:	Journal of Human Genetics [print]
Lokácia:	Roč. 55, č. 12. - Londýn : Springer Nature, (2010), s. 834-837
ISSN:	1434-5161. - ISSN 1435-232X
Ohlas:	[1] 2011. JEN, J.C. Genetics of vestibulopathies. In Advances in oto-rino-laryngology, ISSN 0065-3071. 2011, vol. 70, s. 130-134.
Ohlas:	[1] 2011. HIETIKKO, E., KOTIMÄKI, J., KENTALA, E. et al. Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings. In Genetics in medicine, ISSN 1098-3600. 2011, vol. 13, no. 5, s. 415-420.
Ohlas:	[1] 2011. GAZQUEZ, I., LOPEZ-ESCAMEZ, J.A. Genetics of recurrent vertigo and vestibular disorders. In Current genomics, ISSN 1389-2029. 2011, vol. 12, no. 6, s. 443-450.
Ohlas:	[1] 2011. EPPSTEINER, R.W., SMITH, R.J.H. Genetic disorders of the vestibular system. In Current opinion in otolaryngology and head and neck surgery, ISSN 1068-9508. 2011, vol. 19, no. 5, s. 397-402.
Ohlas:	[1] 2012. GASQUEZ, I., REQUENA, T., ESPINOSA, J.M. et al. Genetic and clinical heterogeneity in Meniere`s disease. In Autoimunity reviews, ISSN 1568-9972. 2012, vol. 11, no. 12, s. 925-926.
Ohlas:	[1] 2012. NOGUCHI, Z. Meniere`s disease and gene. In Equilibrium research, ISSN 0385-5716. 2012, vol. 71, no. 4, s. 247/251.
Ohlas:	[1] 2012. HIETIKKO, E., KOTIMÄKI, J., OKULOFF, A. et al. A replication study on proposed candidate genes in Méniere`s disease, and a review of the current status of genetic studies. In International journal of audiology, ISSN 1499-2027. 2012, vol. 51, no. 11, s. 841-845.
Ohlas:	[1] 2013. HIETIKKO, E., KOTIMÄKI, J., SORRI, M. et al. High incidence of meniere-like symptoms in relatives of meniere patients in the areas of Oulu University Hospital and Kainuu Central Hospital in Finland. In European journal of medical genetics, ISSN 1769-7212. 2013, vol. 56, no. 6, s. 279-285.
Ohlas:	[1] 2014. REQUENA, T., ESPINOSA-SÁNCHEZ, J.M., CARBRERA, S. et al. Familial clustering and genetic heterogeneity in Meniere's disease. In Clinical genetics, ISSN 0009-9163. 2014, vol. 85, no. 3, s. 245-252.
Ohlas:	[1] 2015. REQUENA, T., CABRERA, S., MARTIN-SIERRA, C. et al. Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere`s disease. In Human molecular genetics, ISSN 0964-6906. 2015, vol. 24, no. 4, s. 1119-1126.
Ohlas:	[1] 2015. LOPEZ-ESCAMEZA, J.A., CAREY, J., CHUNG, W-H. et al. Diagnostic criteria for Meniere's disease. In Journal of vestibular research-equilibrium & orientation, ISSN 0957-4271. 2015, vol. 25, no. 1, s. 1-7.
Ohlas:	[1] 2015. CHIARELLA, G., PETROLO, C., CASSANDRO, E. The genetics of Méniere's disease. In Application of clinical genetics, ISSN 1178-704X. 2015, vol. 8, s. 9-17.
Ohlas:	[1] 2020. ESCALERA-BALSERA, A., ROMAN-NARANJO, P., LOPEZ-ESCAMEZ, J.A. Systematic review of sequencing studies and gene expression profiling in familial meniere disease. In Genes, ISSN 2073-4425. 2020, roč. 11, č. 12, art. no. 1414. SCOPUS;WOS:000602160600001.
Ohlas:	[1] 2020. GALLEGO-MARTINEZ, A., LOPEZ-ESCAMEZ, J.A. Genetic architecture of Meniere's disease. In Hearing research, ISSN 0378-5955. 2020, roč. 367, art. no. 107872. SCOPUS;WOS:000591555600006.
Ohlas:	[1] 2020. PEREZ-CARPENA, P., LOPEZ-ESCAMEZ, J.A. Current understanding and clinical management of Meniere's disease: a systematic review. In Seminars in neurology, ISSN 0271-8235. 2020, roč. 40, č. 1, s. 138-150. SCOPUS;WOS:000519106600016.
Ohlas:	[1] 2017. LOPEZ-ESCAMEZ, J.A., CAREY, J., CHUNG, W.H. et al. Diagnostic criteria for Meniere's disease according to the classification committee of the Bárány society. In HNO, ISSN 0017-6192. 2017, roč. 65, č. 11, s. 887-893. SCOPUS;WOS:000414501800004.
Ohlas:	[1] 2017. MARTÍN-SIERRA, C., GALLEGO-MARTINEZ, A., REQUENA, T. et al. Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease. In European journal of human genetics, ISSN 1018-4813. 2017, roč. 25, č. 2, s. 200-207. SCOPUS;WOS:000394122900012.
Ohlas:	[1] 2017. OBERMAN, B.S., PATEL, V.A., CUREOGLU, S. et al. The aetiopathologies of Ménière’s disease: a contemporary review. In Acta Otorhinolaryngologica Italica, ISSN 0392-100X. 2017, roč. 37, č. 4, s. 250-263. SCOPUS;WOS:000410293200002.
Ohlas:	[1] 2016. ESPINOSA-SANCHEZ, J.M., LOPEZ-ESCAMEZ, J.A. Menière's disease. In Handbook of clinical neurology , ISSN 0072-9752. Amsterdam : Elsevier B.V., 2016, roč. 137, s. 257-277. SCOPUS;WOS:000403758200021.
Ohlas:	[1] 2016. LOPEZ-ESCAMEZ, J.A., CAREY, J., CHUNG, W.H. et al. Diagnostic criteria for Menière's disease: Consensus document of the Bárány Society, the Japan Society for Equilibrium Research, the European Academy of Otology and Neurotology (EAONO), the American Academy of Otolaryngology-Head and Neck Surgery (AAO-HNS) and the Korean Balance Society. In Acta Otorrinolaringologica Espanola, ISSN 0001-6519. 2016, roč. 67, č. 1, s. 1-7. SCOPUS;WOS:000399092600004.
Ohlas:	[1] 2023. DAI, Q., LONG, L., ZHAO, H. et al. Genetic advances in meniere disease. In Molecular biology reports, ISSN 0301-4851. 2023, roč. 50, č. 3, s. 2901-2908. WOS:000903436700009; SCOPUS.