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Results 1-10 of 15 (Search time: 0.003 seconds).
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Issue DateTitleAuthor(s)
6-Jul-2021Glutathione reductase is associated with the clinical outcome of septic shock in the patients treated using continuous veno-venous haemofiltrationMoisejevs, Georgijs; Bormane, Eva; Trumpika, Dace; Baufale, Regina; Busmane, Inara; Voicehovska, Julija; Grigane, Anda; Suba, Olegs; Silova, Alise; Skesters, Andrejs; Lejnieks, Aivars; Gailite, Linda; Brigis, Girts; Department of Internal Diseases; Scientific Laboratory of Biochemistry; Scientific Laboratory of Molecular Genetics; Department of Public Health and Epidemiology
Dec-2021A novel EDA variant causing X-linked hypohidrotic ectodermal dysplasia : Case reportAlksere, Baiba; Kornejeva, Liene; Grinfelde, Ieva; Dzalbs, Aigars; Enkure, Dace; Conka, Una; Andersone, Santa; Blumberga, Arita; Nikitina-Zake, Liene; Kangare, Liga; Radovica-Spalvina, Ilze; Vasiljeva, Inta; Gailite, Linda; Erenpreiss, Juris; Fodina, Violeta; Rīga Stradiņš University
2020Clinical and neurophysiological spectrum of polyneuropathies in childrenMillere, Elīna; Gribuste, Laura; Kazaine, Inese; Strautmanis, Jurgis; Gailite, Linda; Kenina, Viktorija; Rīga Stradiņš University
31-May-2023Oral Microbiome Traits of Type 1 Diabetes and Phenylketonuria Patients in LatviaAbola, Iveta; Gudra, Dita; Ustinova, Maija; Fridmanis, Davids; Emulina, Darta Elizabete; Skadins, Ingus; Brinkmane, Anda; Lauga-Tunina, Una; Gailite, Linda; Auzenbaha, Madara; Scientific Laboratory of Molecular Genetics; Department of Conservative Dentistry and Oral Health; Department of Biology and Microbiology
23-Jun-2021GJB1 Gene Analysis in Two Extended Families with X-Linked Charcot-Marie-Tooth DiseaseKovale, Sabine; Terauda, Ruta; Millere, Elina; Taurina, Gita; Murmane, Daiga; Isakova, Jekaterina; Kenina, Viktorija; Gailite, Linda; Scientific Laboratory of Molecular Genetics
Mar-2022New-Born Screening for Spinal Muscular Atrophy : Results of a Latvian Pilot StudyGailite, Linda; Sterna, Olga; Konika, Maija; Isakovs, Aleksejs; Isakova, Jekaterina; Micule, Ieva; Setlere, Signe; Diriks, Mikus; Auzenbaha, Madara; Scientific Laboratory of Molecular Genetics
3-Oct-2018Case report : Multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndromeGailite, Linda; Rots, Dmitrijs; Pukite, Ieva; Cernevska, Gunta; Kreile, Madara; Scientific Laboratory of Molecular Genetics
2019Novel variant of the androgen receptor gene in a patient with complete androgen insensitivity syndrome and polyorchidismKonrade, Ilze; Zavorikina, Julija; Fridvalde, Aija; Rots, Dmitrijs; Kalere, Ieva; Strumfa, Ilze; Dambrova, Maija; Gailite, Linda; Department of Internal Diseases; Scientific Laboratory of Molecular Genetics; Faculty of Pharmacy; Department of Pathology; Department of Human Physiology and Biochemistry
5-Oct-2022Alanyl-tRNA synthetase 1 gene variants in hereditary neuropathy genotype and phenotype overviewSetlere, Signe; Jurcenko, Marija; Gailite, Linda; Rots, Dmitrijs; Kenina, Viktorija; Department of Doctoral Studies; Scientific Laboratory of Molecular Genetics; Department of Biology and Microbiology
Jun-2022Dentalni status i parodontološko zdravlje pacijenata s fenilketonurijom u LatvijiAbola, Iveta; Emulina, Darta Elizabete; Skadins, Ingus; Brinkmane, Anda; Gailite, Linda; Auzenbaha, Madara; Scientific Laboratory of Molecular Genetics; Department of Conservative Dentistry and Oral Health; Department of Biology and Microbiology