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Vaccine|July 16, 2017
Repeated seasonal influenza vaccination among elderly in Europe: Effects on laboratory confirmed hospitalised influenzaMarc Rondy, Odile Launay, Jesus Castilla, et al.
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University|December 22, 2017
Antihypertensive treatment prescription in pediatric dialysis patients in Poland: A comparison between two nationwide studies 2003/2004-2013Krzysztof Wróblewski, Karolina Hincz, Monika Miklaszewska, et al.
Przeglad Lekarski|August 11, 2006
[Congenital and genetic related causes of end-stage renal disease--data from Polish Registry of Renal Rreplacement Therapy in Children 2000-2004]Aleksandra Zurowska, Ilona Zagozdzon, Irena Bałasz, et al.
Genomics|May 11, 2020
Parental somatic mosaicism for CNV deletions - A need for more sensitive and precise detection methods in clinical diagnostics settingsQian Liu, Justyna A Karolak, Christopher M Grochowski, et al.
Journal of the Neurological Sciences|May 12, 2009
Incidence and factors associated with treatment failure in the CLIMB multiple sclerosis cohort studyS A Gauthier, B I Glanz, M Mandel, et al.
Genes, Chromosomes & Cancer|February 16, 2012
High-resolution genome-wide copy-number analysis suggests a monoclonal origin of multifocal prostate cancerLara K Boyd, Xueying Mao, Liyan Xue, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 25, 2010
Severe mental retardation, seizures, and hypotonia due to deletions of MEF2CBeata A Nowakowska, Ewa Obersztyn, Krystyna Szymańska, et al.
Human Molecular Genetics|April 25, 2015
Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3Shen Gu, Bo Yuan, Ian M Campbell, et al.
Journal of Endocrinological Investigation|May 14, 2008
Effectiveness of the iodine prophylaxis model adopted in PolandZ Szybinski, F Golkowski, M Buziak-Bereza, et al.
Medycyna Wieku Rozwojowego|February 5, 2013
Assessment of the role of copy-number variants in 150 patients with congenital heart defectsKatarzyna Derwińska, Magdalena Bartnik, Barbara Wiśniowiecka-Kowalnik, et al.
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