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Results 11-18 of 18 (Search time: 0.002 seconds).
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Issue DateTitleAuthor(s)
1-Aug-2018Performance comparison of two whole genome amplification techniques in frame of multifactor preimplantation genetic testingVolozonoka, Ludmila; Perminov, Dmitry; Korņejeva, Liene; Alkšere, Baiba; Novikova, Natālija; Pīmane, Evija Jokste; Blumberga, Arita; Kempa, Inga; Miskova, Anna; Gailīte, Linda; Fodina, Violeta; Scientific Laboratory of Molecular Genetics; Department of Obstetrics and Gynaecology
14-Apr-2012Challenges in the management of a patient with Cowden syndrome : Case report and literature reviewMelbarde-Gorkuša, Inga; Irmejs, Arvids; Berziņa, Dace; Štrumfa, Ilze; Aboliņš, Arnis; Gardovskis, Andris; Subatniece, Signe; Trofimovičs, Genadijs; Gardovskis, Janis; Miklaševičs, Edvins; Hereditary Cancer Research Department
13-Aug-2019Meta-analysis of cancer triploidy : Rearrangements of genome complements in male human tumors are characterized by XXY karyotypesVainshelbaum, Ninel M.; Zayakin, Pawel; Kleina, Regina; Giuliani, Alessandro; Erenpreisa, Jekaterina; Department of Pathology
Dec-2012Strategies to work with HLA data in human populations for histocompatibility, clinical transplantation, epidemiology and population genetics : HLA-NET methodological recommendationsSanchez-Mazas, A.; Vidan-Jeras, B.; Nunes, J. M.; Fischer, G.; Little, A. M.; Bekmane, U.; Buhler, S.; Buus, S.; Claas, F. H.J.; Dormoy, A.; Dubois, V.; Eglite, E.; Eliaou, J. F.; Gonzalez-Galarza, F.; Grubic, Z.; Ivanova, M.; Lie, B.; Ligeiro, D.; Lokki, M. L.; da Silva, B. Martins; Martorell, J.; Mendonça, D.; Middleton, D.; Voniatis, D. Papioannou; Papasteriades, C.; Poli, F.; Riccio, M. E.; Vlachou, M. Spyropoulou; Sulcebe, G.; Tonks, S.; Nevessignsky, M. Toungouz; Vangenot, C.; van Walraven, A. M.; Tiercy, J. M.; Rīga Stradiņš University
18-Sep-2014Rare diseases and orphan drugs : Latvian storyLogviss, Konstantins; Krievins, Dainis; Purvina, Santa; Department of Internal Diseases
11-May-2016Impact of orphan drugs on Latvian budgetLogviss, Konstantins; Krievins, Dainis; Purvina, Santa; Department of Pharmacology
1-Jan-2016Mounier-Kuhn syndrome : A systematic analysis of 128 cases published within last 25 yearsKrustins, Eduards; Department of Internal Diseases
Sep-2011Whole Xp deletion in a girl with mental retardation, epilepsy, and biochemical features of OTC deficiencyJoost, K.; Tammur, P.; Teek, R.; Žilina, O.; Peters, M.; Kreile, M.; Lace, B.; Žordania, R.; Talvik, I.; Õunap, K.

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